JP2020528797A - Patient treatment system and method - Google Patents

Abstract

It comprises a system comprising a sensor having electrodes comprising an active electrode and a passive electrode, the sensor making physical contact with the patient's skin to form an electrical circuit with the controller's control electronics, which electrical circuit Electrical parameters can be measured using active and passive electrodes within a closed-loop electrical muscle stimulation system. A sensor can be used to apply a detected electrical pulse to the tissue, electrical parameters are measured from the tissue, and a stimulus pulse is applied to the tissue based at least in part on the measured electrical parameters. The stimulus is tunably controlled by the controller to maintain a constant power output to the tissue based on electrical parameters. The article is coupled to at least one computer-readable medium configured to store the usage data, and the usage data is associated with the patient's use of the article. [Selection diagram] None

Description

This application has priority from US Provisional Application Nos. 62 / 170,001 filed June 2, 2015 and US Provisional Application Nos. 62 / 107,954 filed January 26, 2015. Allegedly a partial continuation of US Patent Application No. 15 / 007,014 filed on January 26, 2016, US Application No. 15 / 663,532 filed on July 28, 2017. Claiming the interests of the issue and claiming priority, the entire contents of which are incorporated herein by reference.

Orthopedic braces and wraps are useful as prophylactic support to prevent damage to the joint caused by joint movement and orientation that deviates from the biomechanical limits of the joint. Orthopedic braces and wraps are also useful for promoting proper healing of joints following joint damage or joint surgery and are used to stabilize joints with arthritis and thereby reduce pain. can do.

An important part of the successful healing process after injury and possible surgery is the rehabilitation process. As a major part of the rehabilitation process, patients usually recover their range of motion after suffering injury, after surgery, or when suffering from a condition that can lead to arthritis, muscle atrophy, Talk to a physiotherapist to strengthen the patient's muscles (s). Knee braces are particularly used in the treatment of various knee disorders. Such braces can be configured to exert force or leverage on the limbs around the knee joint to relieve pressure within a portion of the knee joint or to reduce the load on that portion of the knee. .. In addition, if the knee ligaments are fragile, frail, or surgically repaired, the knee brace can stabilize, protect, support, or rehabilitate the knee. Typical knee braces and knee brace formulations have some significant limitations and drawbacks. First, after the injury has occurred and medical professionals such as doctors have recommended that the patient wear a knee brace, the medical professional will re-introduce the patient for weeks or months after the first visit. You may not see it. Healthcare professionals may not receive any feedback on the range of motion of the joint or the strength of the muscles surrounding the joint.

When the patient wears the brace, the physiotherapist manually adjusts the brace under the guidelines provided by the doctor to reduce or increase the permissible movement of the injured joint or follow muscle atrophy. The loosened brace can be adjusted, or both. Because these manual adjustments are based on the personal judgment of the physiotherapist (or medical professional), for example, the muscles and surrounding tissues may not be strong enough to support the joint. This adjustment is often erroneous.

In some cases, patients receive electrical muscle stimulation (EMS) at the beginning of the physical treatment process and have the ability to voluntarily contract their muscles before exercise and stretching begin. You can recover. EMS, also known as neuromuscular electrical stimulation ("NMES: neuromuscular electrical stimulation"), has been used in therapeutic practice virtually unchanged for the past 30 years. The current model employs a target muscle group and provides electrical stimulation that mimics the action potentials normally generated from neurological signals to activate and manifest the action potentials and the resulting contraction of muscle fibers. , It is intended to contract muscles. Electrical stimulation therapy includes the appropriate level of power and / or duration of the electrical pulse, pulse width, phase characteristics (single-phase, two-phase, three-phase, polyphase, symmetric), frequency, waveform (sine wave, square, triangle). , Trapezoidal, serrated, custom), duty cycle, work cycle on / off time, work cycle can be enhanced by determining the lamp type. EMS is also used by therapists (as prescribed by health care providers) to strengthen atrophied muscles. However, delivery of EMS for muscle strengthening is suboptimal as it is usually performed when the patient is with the therapist. In addition, the physician treating the patient (eg, a surgeon) often sees the patient multiple times after treating the injury (eg, surgery). Physicians usually determine the next step in treating a patient based on how the patient looks and feels during the visit. However, physicians usually do not have objective data related to patient injury to aid the physician's assessment of the patient and the next step in the patient's treatment. Specifically, physicians may not be able to obtain accurate range of motion or muscle strength. As a result, the physician determines the patient's next course of treatment based on his subjective analysis of the patient at the time of the patient's visit, and this analysis may be suboptimal. In addition to the data being suboptimal, the time points at which these data are observed are inadequate and suboptimal. The patient may heal faster or slower than the typical patient, and the patient's treatment can be well customized according to the patient's actual progression.

Therefore, there is still a need for a brace system that can provide monitoring of the brace system in use and provide feedback and adjustment (preferably in real time) of the brace system during the course of treatment.

Some embodiments of the present invention include at least one sensor comprising a plurality of electrodes including at least one active electrode and at least one passive electrode, the at least one sensor physically with the patient's skin. Includes systems configured and arranged to contact and form electrical circuits with at least one controller control electronics. The electrical circuit is configured and arranged to measure electrical parameters using at least one active electrode and said at least one passive electrode to form a closed-loop electrical muscle stimulation system, with at least one active electrode and at least one by a sensor. The stimulation current or voltage applied to the skin between the passive electrodes is based on at least one program and at least one electrical parameter measured through at least one active electrode and at least one passive electrode. In some embodiments, the at least one controller (a) applies a detected electrical pulse to the tissue using at least one sensor, (b) measures at least one electrical parameter from the tissue, and (c). ) Using at least one of the active electrodes, a stimulus pulse is tunably applied to the tissue based at least in part based on the measured electrical parameters, and the stimulus pulse is tunably controlled by at least one controller. It is configured and arranged to maintain a constant power output to the tissue based on at least one electrical parameter, at least in part, and to repeat (d) steps (a)-(c). Some embodiments comprise an article coupled to at least one computer-readable medium configured to store usage data, the usage data relating to patient use of the article.

Some embodiments further include computer programs, applets or applications configured to upload said usage data for analysis. In some embodiments, the at least one controller is configured and arranged to electromagnetically couple with a mobile computing device using at least a portion of a computer program, applet or application. In some embodiments, at least a portion of a computer program, applet or application is configured and arranged to include at least one user interface on a user's computing device, at least one user interface being at least a portion. It is configured to display usage data and allow control of article parameters.

In some embodiments, at least one controller is configured to update at least one user interface with at least one of the state of a portion of the article, the position of a portion of the article, and data from at least one sensor. Will be done. In some embodiments, the at least one user interface comprises a display that includes an option to scan the article and synchronize it with at least one controller. In some embodiments, at least one user interface comprises a display that includes an option to scan and synchronize more than one article. In some embodiments, the at least one user interface comprises a display that includes an option to activate a wired or wireless link that connects the article to at least one controller. In other embodiments, the display is configured and arranged to allow the user to set or reconfigure at least one stimulus pulse.

Some embodiments relate to at least one of the stimuli provided by at least a portion of the article and the range of motion measured by at least a portion of the article by at least a portion of a computer program, applet or application. Includes a display that can be configured to display the above parameters. In some embodiments, the display relates to at least one of the stimuli provided by at least a portion of the article and the range of motion measured by at least a portion of the article by at least a portion of a computer program, applet or application. It can be configured to provide a visual representation of the user's behavior wearing at least a portion of the article.

In some embodiments, the computing device is a desktop computer, laptop computer, digital tablet, digital information terminal, mobile phone or smartphone, smartwatch, wearable activity monitor, glasses, camera, pager, and internet appliance. It has at least one. In some embodiments, the article comprises a brace assembly. In some embodiments, the brace assembly comprises at least one of a brace, stay, sleeve, band, sling, garment, wrap, and strap.

In some embodiments, the at least one sensor is an accelerometer, motion sensor, proximity sensor, optical sensor, motion sensor, gyromometer, magnetometer, proximity sensor, hydration sensor, force or pressure sensor, position sensor, all. Earth positioning sensor (GPS), optical sensor, magnetic sensor, magnetometer, induction sensor, capacitance sensor, eddy current sensor, resistance sensor, magnetic resistance sensor, induction sensor, infrared sensor, tilt meter sensor, piezoelectric material or piezoelectric It includes a base sensor, a blood oxygen sensor, a heart rate sensor, a laser or ultrasonic base sensor, and an electromyogram type sensor.

Some embodiments are computer programs, applets or applications configured to initiate or maintain the exchange of usage data between the article and the server and / or between the combined mobile computing device and the server. Includes remote servers including. In some embodiments, the server is configured as a host to a web portal or is coupled to a host server that provides the web portal, which is the usage data or at least one associated with the use of at least a portion of the article. It is configured to access or display parameters.

In some embodiments of the invention, the web portal is configured to generate one or more alerts based on at least one user customization criteria related to usage data, which criteria are at least one article by the user. Partial usage level, usage limit of at least part of the article by the user, usage time of at least part of the article by the user, usage type of at least part of the article by the user, and / or behavior of at least part of the article in use by the user. Can include.

In some embodiments, the alert comprises at least one of an email, text or SMS message, display icon, rendered text, rendered graphic, categorized or customized alert. In some other embodiments, at least one user customization criterion is a monitoring window, utilization and / or activity level, one or more designated compliance or rehabilitation goals, compliance rate, range of motion (ROM), and pain. Contains at least one of the values.

Shown is a knee brace according to an embodiment of the invention that includes two sets of geometric structures, each coupled to one rigid segment for a joint. A knee brace including stay and lap components according to some embodiments of the present invention is shown. A brace sensor for motion data capture and motion capture from a brace according to some embodiments of the present invention is shown. Some of the knee wraps according to some embodiments of the present invention are shown. Knee wraps according to some embodiments of the present invention are shown. Demonstrates a brace system with a combined modular orthopedic brace and conductive wrap according to some embodiments of the present invention. A side view shows a combined modular orthopedic brace and conductive wrap according to some embodiments of the present invention. The shoulder sling according to some embodiments of the present invention is shown. A wrist brace comprising a plurality of sensors according to some embodiments of the present invention is shown. The rear view of the full shoulder vest according to some embodiments of the present invention is shown. The rear view of the full shoulder vest according to some embodiments of the present invention is shown. The front view of the full shoulder vest according to some embodiments of this invention is shown. A full shoulder vest showing an integrated sling according to some embodiments of the present invention is shown. A full shoulder vest showing electrode compression straps according to some embodiments of the present invention is shown. A full shoulder vest showing a median vest closure according to some embodiments of the present invention is shown. A full shoulder vest showing electrode access and trapezius compression straps according to some embodiments of the present invention is shown. It is a rear view of the half vest according to some embodiments of this invention. It is an enlarged rear view of the half vest according to some embodiments of this invention. It is a front view of the half vest according to some embodiments of this invention. It is a front perspective side view of the half vest according to some embodiments of this invention. An air bladder according to some embodiments of the present invention is shown. An air bladder according to some embodiments of the present invention is shown. An arm brace comprising a plurality of accelerometer sensors according to some embodiments of the present invention is shown. A calf brace 470 comprising a plurality of accelerometer sensors according to some embodiments of the present invention is shown. Ankle braces comprising multiple accelerometer sensors according to some embodiments of the present invention are shown. In some embodiments of the invention, the inner region of the brace showing the two contact points used to determine if the brace is worn by a person is shown. FIG. 5 is a front view of a hip brace assembly having an integrated sensor according to some embodiments of the present invention. FIG. 5 is a side view of a hip brace assembly having an integrated sensor according to some embodiments of the present invention. It is a rear view of a hip brace assembly having an integrated sensor according to some embodiments of the present invention. FIG. 5 is a front view of an abdominal / back device having an integrated sensor according to some embodiments of the present invention. FIG. 3 is a rear view of an abdominal / back device having an integrated sensor according to some embodiments of the present invention. A radio aggregate of data including cellular data from a knee brace according to some embodiments of the present invention is shown. The radio data transfer data between the knee brace and the controller according to some embodiments of the present invention is shown. A computer system controller according to some embodiments of the present invention is shown. A computer system including a back-end server according to some embodiments of the present invention is shown. Shown is a screen image showing the current state of the brace, including representation of the degree of bending and orientation with respect to the ground, according to some embodiments of the invention. FIG. 5 shows a diagram of a brace system having a kinematic data acquisition sensor according to some embodiments of the present invention. FIG. 6 shows a diagram of possible motion of various parts of the brace system that can be monitored in the brace system shown in FIG. 7 according to some embodiments of the present invention. FIG. 6 shows a diagram of possible motion of various parts of the brace system that can be monitored in the brace system shown in FIG. 7 according to some embodiments of the present invention. A sensor assembly for detecting surface edema through optical detection according to some embodiments of the present invention is shown. A system for non-anesthetic pain relief using electrical stimulation therapy to nullify pain impulses according to some embodiments of the present invention is shown. Biological feedback data collection according to some embodiments of the present invention is shown. The smart electrodes according to some embodiments of the present invention are shown. Adaptive electrodes according to some embodiments of the present invention are shown. Adaptive electrodes according to some embodiments of the present invention are shown. Adaptive electrodes according to some embodiments of the present invention are shown. NMES postoperative oscilloscope scans of pulse trains according to some embodiments of the invention are shown. NMES postoperative oscilloscope scans of individual pulses of the channel according to some embodiments of the invention are shown. NMES postoperative oscilloscope scans of individual pulses of the channel according to some embodiments of the invention are shown. NMES intensity oscilloscope scans of pulse trains according to some embodiments of the present invention are shown. NMES intensity oscilloscope scans of individual pulses of the channel according to some embodiments of the invention are shown. NMES intensity oscilloscope scans of individual pulses of the channel according to some embodiments of the invention are shown. A TENS oscilloscope scan of a pulse train according to some embodiments of the present invention is shown. A TENS oscilloscope scan of individual pulses according to some embodiments of the invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. The display portion of the treatment system control GUI according to some embodiments of the present invention is shown. The display portion of the treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A display of a treatment system control GUI according to some embodiments of the present invention is shown. A part of the stimulation circuit of the treatment control system according to some embodiments of the present invention is shown. Various displays of a therapeutic system control GUI according to some embodiments of the present invention are shown. Various displays of a therapeutic system control GUI according to some embodiments of the present invention are shown. Various displays of a therapeutic system control GUI according to some embodiments of the present invention are shown. Various displays of a therapeutic system control GUI according to some embodiments of the present invention are shown. Various displays of a therapeutic system control GUI according to some embodiments of the present invention are shown. Various displays of a therapeutic system control GUI according to some embodiments of the present invention are shown. Various displays of a therapeutic system control GUI according to some embodiments of the present invention are shown. Various displays of a therapeutic system control GUI according to some embodiments of the present invention are shown. Various displays of a therapeutic system control GUI according to some embodiments of the present invention are shown. Various displays of a therapeutic system control GUI according to some embodiments of the present invention are shown. Various displays of a therapeutic system control GUI according to some embodiments of the present invention are shown. A therapeutic system according to some embodiments of the present invention is shown. The data types for the treatment system of FIG. 75 according to some embodiments of the present invention are shown. The data categories exchanged between and stored within the components of the treatment system of FIG. 75 according to some embodiments of the present invention are shown. Shown is a provider portal dashboard according to some embodiments of the present invention. Shown are customizable panels and alert windows for provider portal dashboards according to some embodiments of the present invention. Shown is a provider portal patient list window according to some embodiments of the present invention. A patient overview window according to some embodiments of the present invention is shown. A tabular diagram of a patient overview window according to some embodiments of the present invention is shown. A printable patient summary chart according to some embodiments of the present invention is shown. A printable patient summary chart according to some embodiments of the present invention is shown. A printable patient summary chart according to some embodiments of the present invention is shown. A printable patient summary chart according to some embodiments of the present invention is shown. A detailed window of patient stimulation according to some embodiments of the present invention is shown. A detailed window of patient range of motion (ROM) according to some embodiments of the present invention is shown. A patient pain detail window according to some embodiments of the present invention is shown. A patient pain detail window according to some embodiments of the present invention is shown. The patient passive range of motion (PROM) n according to some embodiments of the present invention is shown. The start screen of the mobile application according to some embodiments of the present invention is shown. A scan screen of a mobile application according to some embodiments of the present invention is shown. An information screen of a mobile application according to some embodiments of the present invention is shown. The start stimulus screen of the mobile application according to some embodiments of the present invention is shown. A dashboard screen of a mobile application according to some embodiments of the present invention is shown. The stimulator session start screen of the mobile application according to some embodiments of the present invention is shown. The pain survey screen of the mobile application according to some embodiments of the present invention is shown. The stimulus treatment screen of the mobile application according to some embodiments of the present invention is shown. The stimulation level information screen of the mobile application according to some embodiments of this invention is shown. The stimulation level screen of the mobile application according to some embodiments of this invention is shown. The stimulation level screen of the mobile application according to some embodiments of this invention is shown. The stimulation level screen of the mobile application according to some embodiments of this invention is shown. The stimulation level information screen of the mobile application according to some embodiments of this invention is shown. The range of motion (ROM) start screen of the mobile application according to some embodiments of the present invention is shown. The range of motion (ROM) connection screen of the mobile application according to some embodiments of the present invention is shown. The range of motion (ROM) measurement screen of the mobile application according to some embodiments of the present invention is shown. The range of motion (ROM) measurement screen of the mobile application according to some embodiments of the present invention is shown. The range of motion (ROM) result screen of the mobile application according to some embodiments of the present invention is shown. The setting screen of the mobile application according to some embodiments of this invention is shown. A profile screen of a mobile application according to some embodiments of the present invention is shown. Shows one's own set goal screen of a mobile application according to some embodiments of the present invention. The stimulation help screen of the mobile application according to some embodiments of this invention is shown.

Prior to elaborating on any embodiment of the invention, it is understood that the invention is not limited in its application to the details of the structure and arrangement of components described in the following description or shown in the accompanying drawings. I want to. The present invention can be made in other embodiments and can be carried out in various ways. Similarly, it should be understood that the expressions and terms used herein are for illustration purposes only and should not be considered limiting. The use of "inclusion", "comprising", or "having", and variants thereof herein, includes the items listed below and their equivalents and further items. Means. Unless otherwise stated or limited, the terms "mounted", "connected", "supported", and "combined", as well as their variants, are widely used and directly and indirectly. Includes both mounting, connecting, supporting, and coupling. Furthermore, "connected" and "combined" are not limited to physical or mechanical connections or connections.

The following considerations are presented to allow one of ordinary skill in the art to implement and use embodiments of the present invention. Various modifications to the exemplary embodiments will be readily apparent to those skilled in the art, and the general principles herein apply to other embodiments and applications without departing from the embodiments of the present invention. can do. Accordingly, embodiments of the present invention are not intended to be limited to exemplary embodiments, but the broadest scope consistent with the principles and features disclosed herein should be acknowledged. The following detailed description should be read with reference to drawings with similar elements but with similar reference numbers in different figures. Each figure is not necessarily on scale and depicts selected embodiments and is not intended to limit the scope of embodiments of the present invention. Those skilled in the art will appreciate that the examples provided herein have many useful alternatives and are within the scope of the embodiments of the present invention.

FIG. 1A is a diagram of a knee brace 100 in which one or more stays are coupled to the user (user legs are shown). In some embodiments, the knee brace 100 may comprise a stay 105 that is movably coupled to the stay 110 through the pivotal region 115. When positioned in this way, the knee brace 100 comprises two sets of geometric structures, the stay 105 freely moving relative to the stay 110 and pivoting and / or moving around the pivot region 115. can do. In some embodiments of the invention, the knee brace 100 and any of the brace systems or assemblies disclosed herein are systems for determining the position data of any component or part of the brace system and A method can be provided. For example, in some embodiments, one or more sensors are integrated or coupled to at least a portion of the brace system and also measure or monitor user parameters, track the functional characteristics of the brace system, and / or It can be used to monitor the user's environment. In some embodiments, one or more sensors are integrated or coupled to at least a portion of the brace system and, while attached to the user, are absolute or relative to any part of the brace system. Can be used to measure position and / or movement. In some embodiments, the wrap can be used without a brace and can fully support the sensors and other components disclosed herein as being attached to the brace. .. In some embodiments, one or more sensors can be added to any rigid portion of the brace system. For example, in some embodiments, the knee brace 100 may include at least one sensor coupled to at least one of the stays 105, 110. For example, in some embodiments, the knee brace 100 may include a sensor 120 coupled to a stay 105. In some further embodiments, the knee brace 100 can include a sensor 125 coupled to a stay 110. Sensors 120, 125 can include triaxial movement by coupling to stays 105, 110. Further, the sensors 120 and 125 can move independently of each other in three dimensions according to the movement of the user. In some embodiments, the stay 105 can be coupled to the upper portion 132 of the wrap 130 for positioning in close proximity to or adjacent to the user's thigh, and the stay 110 can be attached to the user. It can be attached to the lower portion 134 of the wrap 130 for positioning in close proximity or adjacent to the lower leg. For example, FIG. 1B shows a knee brace 100 including stays 105, 110 and lap 130 according to some embodiments of the present invention. In some embodiments, the wrap 130 can include a breathable, highly compressed and non-slip material. In some embodiments, sensors 120, 125 position and / or move and accelerate any one set of geometrical structures of the brace 100 on any x, y, and / or z axis. Can be measured at. In some embodiments, the sensors 120, 125 can be coupled to the outer surface of any portion of the brace 100, including, for example, a location within the lap 130 or stay 105, 110 system shown in FIG. 1B. In some embodiments, the sensor can be integrated with the brace 100 by integrating it within an internal portion of the brace 100 or by coupling it to the outer surface of the brace 100.

In some embodiments of the invention, the sensor can include an accelerometer. For example, in some embodiments, the sensor can include one or more small solid or microelectromechanical system (MEMS) accelerometers, gyroscopes, and / or magnetometers, which are of the brace system. Combined into one or more parts, it can be used to measure / detect position and orientation, acceleration, velocity, vibration, or impact along a single axis or multiple axes. In some embodiments of the invention, the sensor may include at least one Hall effect sensor. In some further embodiments, the brace system can be used in combination with a magnetic sensor and can include one or more magnets coupled to a predetermined portion of the brace system. For example, some embodiments of the invention may include at least one Hall effect sensor, the at least one Hall effect sensor being used with one or more magnets to move at least a portion of the brace system. Can be determined. For example, in some embodiments, the sensor can determine the rotation of the brace system relative to a fixed point on the hinge.

Some embodiments of the present invention include brace systems or assemblies capable of capturing range of motion (“ROM”). In some embodiments, range of motion data is used preoperatively to undergo surgery, which may indicate that swelling and soft tissue mobility are at acceptable levels for surgery. It is possible to determine when the patient has fully recovered from the initial traumatic injury. In some further embodiments, range of motion data can be used postoperatively to determine when the patient recovers (and thus can be used to determine the rate of recovery from surgery). ). For example, FIG. 1C shows an example of range of motion data capture from the brace system 140. In some embodiments, position data can be added to any brace system 140 having one or more rigid structures to which one or more motion sensors can be coupled. For example, in some embodiments, the brace system 140 may include a stay 145 that includes a coupled sensor 155 and the stay 150 may include a coupled sensor 160. In some embodiments, the brace sensors 155, 160 may include one or more accelerometers, gyroscopes, and / or position encoders that are coupled to at least one rigid portion of the brace system. In some embodiments, as one or both of the stays 145, 150 move, rotate, or pivot around the joint 170, sensors 155, 160 are used and the patient with respect to the current range of motion. Can give active feedback to. In some embodiments, range of motion data can be used to provide continuous feedback to the user, thereby encouraging the user to stretch muscles or move joints during the recovery phase. .. For example, in some embodiments, palpable feedback can be provided whenever the user exceeds a specified maximum range of motion. Further, in some embodiments, the brace system 140 can be used to warn the user when the user has reached a range of motion that is not considered safe based on the user's recovery stage. In some other embodiments, the brace system 140 can incorporate dynamic resistance, spring constant, and / or force or damping to protect the joint if high acceleration or range of motion is detected. In some embodiments, this can be achieved using magnetic rheological fluids, inertial valve designs, piezoelectric springs / materials, and the like. Some embodiments of the present invention include a kinematic data acquisition sensor for measuring the position and movement of the brace system 140. Further, in some embodiments, the brace system 140 may include a range of motion sensor for any brace system that includes one or more hinge features. In some embodiments, the sensor can include indexing points so that the absolute position is determined. Some embodiments of the present invention include proximity or contact-based sensors to determine where a set point on the hinge is in close proximity to the sensor. In some embodiments, the sensors are light (shadow, self-imaging, or interference) sensors, magnetic sensors, inductive sensors, capacitance sensors, eddy current sensors, resistance sensors, magnetic resistance sensors, inductive sensors, infrared sensors. , Accelerator sensor, tilt meter sensor, piezoelectric sensor and the like.

In some embodiments of the invention, any of the brace systems or assemblies disclosed herein can include one or more controllers. In some embodiments, the controller can be integrated and / or coupled to a stay, joint, pivot, or wrap of the brace system. For example, in some embodiments of the invention, the control electronics include a pivot joint configured to allow the brace of the brace system to flex (eg, during patient flexion and extension). be able to. The pivot joint can include a solenoid and an accelerometer to lock the brace (eg, after detecting stress). In one embodiment, the pivot joint comprises a digital position encoder that determines the absolute position of the joint. The position encoder can allow adjustment of the physical resistance applied to the joint as the patient moves the joint. Brace control electronic devices can include communication modules (eg, transmitters or transmitters / receivers or wires) for communicating with computing devices.

Some embodiments include a dynamic bracing system with integrated electrical stimulation that can be configured to assist in achieving joint flexion and / or extension. In some embodiments, one or more linear springs, torsion springs, and / or cam-based systems can be used to provide dynamic bracing options. In some embodiments, the brace system can comprise a hip brace with integrated electrical stimulation to provide NMES treatment to the target tissue within the pelvic region.

In some embodiments, one or more sensors can be integrated within a wearable wrap or garment. For example, FIG. 1D shows a portion of the knee wrap 180 according to some embodiments of the present invention, and FIG. 1E shows a portion of the knee wrap 180. As illustrated, in some embodiments, the knee wrap 180 may include a main body wrap 185 that includes a non-slip compression material 187. In some embodiments, the material can assist in preventing the knee wrap 180 from moving when positioned on the wearer by frictional and compressive forces. In some embodiments, the main body wrap 185 can include various extensions 189 that allow the wrap 180 to be wrapped and attached to the user's knees and also accommodates different parts of the wearer's body. It can include various apertures. For example, in some embodiments, the knee wrap 180 may include a popliteal cutout 191 corresponding to structure and movement near the back of the wearer's knee. Further, in some embodiments, various electronic devices can be coupled or integrated with the main body wrap 185. For example, in some embodiments, the main body wrap 185 can include one or more stimulation electrodes or electrode pairs 195, such as the quadriceps electrodes 195a and / or the calf electrodes 195b. Further, in some embodiments, the electrodes or electrode pairs 195 can be placed on the inner surface 181 of the wrap 180 to allow contact with the wearer's skin. As used herein, each stimulus electrode pair can comprise a first electrode structure having a first polarity and a second electrode structure having a second polarity. Since the first and second polarities can be different, the first and second electrode structures function to form a pair of electrodes capable of electrical stimulation. In some embodiments, the structure of the first electrode can be substantially the same or similar to that of the second electrode. In other embodiments, the structures of the first and second electrodes can be different. In some embodiments, the electrodes are not limited to conventional electrode structures. For example, in some embodiments, one or more electrodes are capable of efficiently transmitting signals, or in some embodiments, while still providing sufficient signal strength for a particular application. Conductive materials with significant loss or degradation can be included. As used herein, the terms "stimulation electrode" and "stimulation electrode pair" can be used interchangeably.

In some embodiments, one or more brace assemblies can be integrated and / or combined with the knee wrap to form a combined modular orthopedic brace and conductive wrap. For example, FIG. 1F shows a brace system 200 with a modular orthopedic brace 210 and a conductive wrap assembly 220 combined according to some embodiments of the invention, and FIG. 1G shows some embodiments of the invention. A side view shows a brace system 200 with a modular orthopedic brace 210 and a conductive wrap assembly 220 combined by. In some embodiments of the invention, the wrap assembly 220 may include a brace strap 230, an inner malleolus pad 235, and a slide lock 240 for positioning, compression, and comfort. Further, in some embodiments, the stimulation module 250 can be coupled to the assembly 220 to allow application of stimulation therapy. Further, in some embodiments, the assembly may include a dial hinge 245 with a ROM stop to allow customized fitting and treatment.

Some embodiments include brace systems or assemblies configured for the target area of the wearer's body. For example, FIG. 2A shows a shoulder sling 300 according to some embodiments of the present invention. In some embodiments, the shoulder sling 300 may include a wrap or partial garment 301 that wraps or surrounds at least a portion of the wearer's body, including at least the shoulder area. In some embodiments, the shoulder sling 300 may include an electrode inside, the electrode being a rotator cuff muscle (eg, supraspinatus, infraspinatus, etc., scapular skin muscle, other muscle groups, etc.) And / or shoulder joints) can be used to stimulate. For example, in some embodiments, the shoulder sling 300 may include an electrode 305 coupled or integrated with the sling 300. Further, in some embodiments, the sling 300 may include at least one accelerometer, the at least one accelerometer moving the wearer, including the movement of the wearer's shoulders with respect to the wearer's torso. Can be measured, monitored, or tracked. For example, in some embodiments, the sling 300 may include an accelerometer 310 that is located at one end of the sling 300 near the wearer's head or neck end. In some further embodiments, the sling 300 may include an accelerometer 310 that is located at one end of the sling 300 near, adjacent to, or close to the wearer's shoulders or arms.

FIG. 2B shows a wrist brace 320 with a wrap 325 configured to wrap or surround the wearer's wrist and / or hand at least partially. In some embodiments, the wrist brace 320 can include multiple sensors 330. In some embodiments, the sensor 330 may include one or more accelerometers. In some further embodiments, motion sensors, proximity sensors, optical sensors, magnetic sensors, inductive sensors, capacitive sensors, eddy current sensors, resistance sensors, magnetic resistance sensors, inductive sensors, infrared sensors, tilt meter sensors. Other types of sensors such as, piezoelectric materials and piezoelectric base sensors can be included. In some embodiments, the wrist brace 320 is also configured to stimulate the distal arm muscle groups and / or wrist joints (s), electrodes 335 placed inside the wrap 325. Can be included.

Some embodiments include wraps, braces, or vests that include an integral support and / or tension member. In some embodiments, the tension or support member can function to provide support and / or tension to the wrap, brace, or vest. For example, FIG. 2C shows a rear view of the Fulsholda Best 350 according to some embodiments of the present invention. In some embodiments, the vest 350 may include one or more internal tension members 355. In some embodiments, one or more of the tension members 355 can function to provide mechanical force to the wearer's body (eg, the wearer's shoulders, etc.) to correct the posture. In some embodiments, the vest 350 may include functional electrodes for posture. For example, FIG. 2D shows a rear view of the full shoulder vest 350 according to some embodiments of the present invention, and FIG. 2E shows a front view of the full shoulder vest 350 according to some embodiments of the present invention. In some embodiments, the vest 350 may include a main vest body 351 that can be closed using one or more closure extensions 372. In some embodiments, the vest 350 can include a paraspinal / scapula stabilizer electrode 362 for posture. In addition, some embodiments may include an air bladder pocket 364 containing at least one air bladder configured for sleep support and electrode compression.

2N and 2P show an air bladder 425 that can be used in various embodiments of the invention described herein. In some embodiments, the air bladder 425 can comprise at least one reversibly expandable bladder 430 coupled to the expansion assembly 433. In some embodiments, the expansion assembly 433 can include a removable expansion tube 440 and a contraction valve 438 coupled to a pump 435 (eg, a manual pump). In some other embodiments, the vest 350 is also integrated by inserting or attaching a heat pack or ice pack in the pocket of the vest or under the shoulder area, in contact with the patient's skin. Thermal or cold treatment can also be included. In addition, some embodiments provide an integrated sling support 358 for the wearer.

Various figures of the full shoulder vest 350 shown on the wearer can be seen in FIGS. 2F-2I. For example, FIG. 2F shows a full shoulder vest 350 showing an integral sling 358 according to some embodiments of the present invention. FIG. 2G shows a full shoulder vest 350 showing an approximate location of the electrode compression strap 368 and the compressed electrode 360, and FIG. 2H shows a midline vest closure including a closure extension 372 according to some embodiments of the invention. The full shoulder best 350 shown is shown. FIG. 2I shows a full shoulder vest 350 showing electrode access and trapezius compression strap 368a according to some embodiments of the invention. In some embodiments, the strap 368 comprises a strap 368a.

Some embodiments include vests that cover other areas of the wearer's upper body. For example, some embodiments include a vest that covers a partial area of the wearer's torso (eg, left, right, or central area). For example, FIG. 2J shows a rear view of a half vest 380 according to some embodiments of the present invention. Further, FIG. 2K shows an enlarged rear view of the half vest 380, and FIG. 2L shows a front view of the half vest 380 according to some embodiments of the present invention. Similar to the Full Best 350 described above, some embodiments may include one or more electrical stimulation electrodes 386. In some embodiments, the half vest 380 may include one or more air bladder pockets 390. Some embodiments include at least one compression strap. For example, as shown in FIG. 2L, in some embodiments, the half vest 380 may include a mitral muscle compression strap 384 attached to the torso wrap 382. The half vest 380 can also include an integral sling 388 coupled to the torso wrap 382. Some embodiments include at least one electrode access opening 400. In addition, some embodiments may include at least one strap or pocket configured to hold or support a portion of the wearer's body. For example, some embodiments include an adjustable quarterback pocket 395 coupled or integrated with the half vest 380. Further, FIG. 2M shows a front side perspective view of the half vest 380 according to some embodiments of the present invention. In some embodiments, the vest 380 may comprise at least one strap or fastener 405, the at least one strap or fastener 405 may be used by the wearer to fasten the vest and tighten the vest. The vest can be loosened, or the vest can be removed.

Moreover, in some embodiments, the vest can include at least one stimulus module 410. In some embodiments, one or more stimulation modules 410 can be integrated within the vest 380. In some further embodiments, one or more stimulation modules 410 are best used with various mounting mechanisms including, but not limited to, fasteners, clips, Velcro, buttons, snap fits, or snap-on assemblies. Can be reversibly fastened to.

FIG. 2Q shows an elbow brace 450 containing multiple accelerometer sensors according to some embodiments of the present invention. In some embodiments, the elbow brace may include an electrode 455 inside the brace 450, which may include the proximal arm muscle group, the distal arm muscle group, and / or the elbow joint (s). May be used to stimulate. In some embodiments, the electrode 455 can be positioned within the upper arm portion 452 of the brace 450 and / or the forearm portion 454 of the brace 450. In some embodiments, the brace 450 can include an accelerometer 460 integrated or coupled to the upper arm portion 452 and an accelerometer 462 integrated or coupled to the forearm portion 454.

FIG. 2R shows a calf brace 470 including a plurality of accelerometer sensors according to some embodiments of the present invention. In some embodiments, the calf brace 470 can be used to stimulate the distal leg muscles and / or knee joints (s) and / or ankle joints (s) on the medial side of the brace 470. Can be equipped with a wrap 475 that also includes a sensor and / or an electrode 480. In some embodiments, the electrode 480 is energized by an electrical stimulus that stimulates the calf muscles to induce an electrical or mechanical pumping effect that pumps body fluids such as blood, thereby reducing edema. Deep vein thrombosis (DVT: deep vein thrombosis) can be prevented.

FIG. 2S shows ankle brace 500 with lap 501 including multiple accelerometer sensors according to some embodiments of the present invention. In some embodiments, the ankle brace 500 is on the medial side of the wrap 501 that can be used to stimulate the distal leg muscles and / or the ankle joints (s) and / or the ankles (s). Can include an electrode 505. The brace 500 may include an accelerometer 510 within the leg portion 503 of the lap 501. In another embodiment, the brace 500 may include an accelerometer 515 within the foot portion 504 of the lap 501.

In some further embodiments, one or more sensors can be coupled to various inner regions of the brace system. For example, FIG. 2T shows the inner region of the brace system and shows two sensors located within the inner region of the brace system. In some embodiments, a predetermined portion of the sensor may comprise a contact point configured located on the outer surface of the brace system inner region. In some embodiments, the sensor can include a human contact sensor, which can be used to determine if the brace is worn by a person. In some embodiments, measurements from sensors can be used to provide patient compliance data in which the use of the brace system is monitored and logged. In some other embodiments, sensors can be used to monitor whether the brace system is properly placed on the user. For example, in some embodiments, the brace 550 may include a main body portion 555 as well as upper and lower strap portions 557 and 559. In some embodiments, the hip brace 550 can include electrodes on the inside of one of the strap portions 557 and 559, which can be used to stimulate muscle groups. For example, in some embodiments, the strap portion 557 may include a plurality of electrodes 560 positioned on various regions of the strap portion 557. Further, in some embodiments, one or both of the strap portions 557 and 559 may include at least one contact sensor. For example, in some embodiments, the strap portion 557 can include at least one integrated or coupled contact sensor 565.

Some embodiments of the invention may include wraps, braces, and / or vests suitable for the wearer's hip area. As with the wraps, braces, and vests described above, some embodiments of the hip device can include various integrated or coupled sensors, electrodes, supports, and / or tension members. .. For example, FIG. 2V shows a front view of a hip brace assembly 570 with an integrated sensor according to some embodiments of the present invention. FIG. 2W shows a side view of the hip brace assembly 570. Further, FIG. 2X shows a rear view of the hip brace assembly 570 with integrated sensors according to some embodiments of the present invention. In some embodiments, the hip brace assembly 570 can include an abdominal / back belt 575, a compression short conductive garment 578, and a brace bar assembly 580. In some embodiments, the brace bar assembly 580 can include an upper bar 582 and a lower bar 584 coupled by a brace hinge 586. In some embodiments, the hip brace assembly 570 is an electrode on the medial side that can be used to stimulate the proximal leg muscles, abductor muscles, adductor muscles, gluteal muscles, and / or gluteal joints. Can also be included. For example, in some embodiments, the hip brace assembly 570 stimulates the abdominal muscles, lower back muscles, and / or back joints (s) and / or pelvic joints (s) and / or hip joints. Can include an abdominal electrode 577 integrated or coupled within the abdominal / back belt 575 used in. In other embodiments, the compressive short conductive garment 578 can include a gluteal muscle group stimulation electrode 590.

In some further embodiments, measurements of the position, movement, and / or acceleration of a portion of the brace assembly can be used to determine the position and movement of the user. For example, in some embodiments, an assembly is used to monitor the user to determine how much time the user spends in an upright position and / or in a supine position. Can be done. In some embodiments, the acceleration data from the brace system can be calculated for each limb and aggregated as a moving average. Further, in some embodiments, this average acceleration value can be used to directly correlate the limbs with the amount of movement of the patient and can also be used as a key to identify a decrease in range of motion. Can be done. For example, the smaller the number, the lower the overall movement level of the user as a whole. In some embodiments, when the maximum number of flexions received from the sensor is high and the average acceleration value is very low, the user is seated in place with the extremities flexed. However, if the average acceleration number is very high and the maximum number of flexions is low, the user is moving around, but with no joint movement, keeping the braced limbs in the locked position. In some other embodiments, using either the integrated or coupled sensors or accelerometers disclosed herein, a free fall incident is determined by one or more sensors in the brace assembly and is computerized. It can be reported to the system (eg, a combined computer, server, back-end system, mobile device, etc. disclosed herein). In some embodiments, the brace system can record free fall to indicate any time the brace (and user) has fallen. Further, in some embodiments, the brace system can determine the height of the fall based on the duration and rate of acceleration. In some embodiments, the brace system can determine if the user has begun to fall and then held up. Further, in some embodiments, the back-end system allows the medical professional to create and / or schedule a follow-up request to determine if the fall actually caused damage. Can be done. Referring to FIG. 2W, in some embodiments, the assembly 570 is integrated into one or more parts of the brace bar assembly 580, including, for example, the upper bar 582 and / or the lower bar 584 and / or the brace hinge 586. A sensor / accelerometer 588 that can be combined and / or combined can be included.

In some further embodiments of the invention, patient compliance data obtained from cumulative measurements from sensors can be stored on a database (eg, in a back-end computer system) and, for example, Used by a physician or medical professional, data from the brace system can be retrieved, reviewed, and / or analyzed. In some embodiments, the physician can utilize the data from the brace in the physician's analysis or patient recommendations. In addition, physicians can utilize data from one patient's brace system when recommending to other patients with similar conditions or injuries. For example, if a doctor tells a patient recovering from ACL reconstruction to run Program 1 during the first week and Program 2 during the second week, and by these programs, If the doctor sees a significant improvement in the patient's strength in the patient's knees, the doctor will probably tell another patient recovering from similar surgery to perform the same program during the same period. In some embodiments, the physician can have a program for a second patient that is updated remotely by a wired or wireless connection to the Internet or a private network. The doctor may then obtain data from both patients to see how they respond to the brace system, and the program is executed by the brace system.

Some embodiments of the invention may include wraps, braces, and / or vests suitable for the wearer's abdominal / back area. As with the wraps, braces, and vests described above, some embodiments of the abdominal / back device include various integrated or coupled sensors, electrodes, supports, and / or tension members. Can be done. For example, FIG. 2Y shows a front view of the abdominal / back device 600 having integrated sensors according to some embodiments of the present invention, and FIG. 2Z shows an abdomen having integrated sensors according to some embodiments of the present invention. / The rear view of the back device 600 is shown. Some embodiments may include a main body 605 with a combined or integrated brace panel 610. In some embodiments, the abdominal electrode 615 can be coupled or integrated with the abdominal / back device 600. In addition, some embodiments include an abdominal / back belt brace 620 coupled to the main body 605. In some embodiments, the abdominal / back belt brace 620 may include one or more coupled or integrated back electrodes 625. Further, as in the other embodiments described above, the abdominal / back device 620 can include one or more optional air bladder for electrode compression and / or back support.

In some embodiments of the invention, the various electronic components can be integrated within one or more modules of the brace system, the modules being able to be combined and recombined into various configurations. For example, in some embodiments, some brace systems or assemblies may comprise a set of modules, each of which has a separate function, and the combination of modules has a different user interface and / or Create a generic NMES platform with different sensors for data collection. In some embodiments, the platform can include at least one stimulus system, one or more sensor systems, and at least one display system. Further, in some embodiments, the brace system can be controlled by a controller in a wired or wireless manner and / or transfer data through the controller. For example, in some embodiments of the invention, any of the brace systems or assemblies described herein can be configured to transmit and / or receive information wirelessly. For example, FIG. 3A wirelessly collects data from the knee brace brace assembly 670, including data communicated through a mobile network 650 and / or WiFi network 655 to a coupled or integrated controller 675 with a wireless antenna 675a. FIG. 6 shows a diagram of a wireless brace system 630 that can be configured for this purpose. In some embodiments, one or more portions of the knee brace assembly 670 are one or more sensors such as sensor 681 coupled to stay 682 and / or sensor 683 coupled to stay 684 (eg, first. The accelerometer or other sensor discussed) can be included and one or more sensors are coupled to controller 675 and wirelessly transmit data from and / or to controllers 676 and / or sensors 681,683. Can be made possible. In some embodiments, a graphical user interface (GUI) 640 is used to control the functionality of various functional aspects of the wireless brace system 630, including any component of the components within the wireless brace system 630. Can and / or can be monitored. In some embodiments, the controller 675 can include rechargeable power and a control unit configured for stimulus and sensor data collection.

In some embodiments, the controller 675 can manage detection and / or stimulation of a patient wearing a brace system or garment (eg, wireless brace system 630, etc.). In some embodiments of the invention, the controller 675 (a) applies at least one stimulus detection pulse to the patient's tissue using at least one sensor and / or electrode, and (b) detection within the tissue. At least one electrical parameter from the patient's tissue associated with pulse power dissipation is measured and (c) at least one stimulus pulse is tunably applied to the patient's tissue based on the measured power dissipation at least in part. Can be configured to: In some embodiments, at least one stimulus pulse may be tunably controlled by at least one controller to maintain a constant power output to the patient's tissue based at least in part on at least one electrical parameter. it can. In some embodiments, steps (a)-(c) can be repeated at least once.

FIG. 3B shows wireless data transfer between the knee brace assembly 670 and the controller 675 according to some embodiments of the present invention. In some embodiments, the radio RF transmission from the brace system 670 has adequate bandwidth from the brace system while minimizing tissue propagation characteristics and specific absorption rates (to avoid tissue heating). It can have sufficient power to enable reliable operation and data transmission and reduce the user's exposure to near-field and long-range RF transmissions. In some embodiments, the brace system 670 is, but not limited to, a zero generation radio signal, a first generation radio signal, a second generation radio signal, a third generation radio signal, a fourth generation radio signal, a fifth generation radio. Signals, arbitrary global positioning satellite signals (such as "GPS" or "GLONASS"), industrial, scientific, and medical (ISM: industrial, scientific and medical) frequency bands (eg, 240-2493.5 MHz), Bluetooth® radio signal (IEEE802.5.4 Bluetooth® class II), RFID electromagnetic radiation, WiFi radio signal, two-way radio RF signal, UHF or VHF signal ("walkie-talkie") It can be configured to transmit and / or receive RF transmissions including civilian band radio signals or other radio signals emitted from type devices), high speed and millimeter wave signals, and near field radio signals. Bluetooth® is a computing and telecommunications industry specification that allows mobile devices to easily interconnect with each other and with non-mobile devices using short-range wireless connections. Describe in detail what can be done. Bluetooth® is available from Bluetooth SIG, Inc. Is a registered trademark of.

In some embodiments, the controller 675 can include a computer system or device. In some embodiments, the brace system can be configured to communicate (eg, wirelessly or by wired connection) with a computing device capable of performing the functions of controller 675. Examples of computing devices are personal computers, digital assistants, personal digital assistants, mobile phones, wearable technology devices (eg smart watches, activity monitors, heart rate monitors, glasses, cameras, etc.), smartphones, tablets, or laptops. Includes, but is not limited to, computers. In some embodiments, the computing device can be a patient device or a device associated with a healthcare professional. Both types of devices can allow healthcare professionals to retrieve and analyze the data transmitted from the brace system. In one embodiment, the data is transmitted in real time so that the healthcare professional can analyze the data and / or adjust the brace at any time. For example, in some embodiments, the patient can access the data using a mobile application on the patient's device. In some further embodiments, physicians and / or therapists can access the data via a web portal. In some embodiments, any data accessed from any of the brace systems of the brace system described herein, including any data collected or streamed through a controller such as controller 675, is 1 or It can be protected using multiple traditional encryption methods. In some embodiments, the protocols and methods for data transfer described are HIPAA compliant.

Referring to FIG. 4, in some embodiments, the brace system or assembly described herein is electronically configured to transfer data from and / or to the brace system 700. Can be combined. Further, in some embodiments, the brace system can also include brace control electronics that can be configured to provide NMES by a program selected from a plurality of programs. In at least one embodiment of the invention, the brace control electronics can be configured to receive a selection of programs by a receiver (eg, from a patient, from a healthcare professional, etc.). In one embodiment, the medical professional can block patient control of the brace (eg, for a period of time). Further, as shown in FIGS. 3A-3B, in some embodiments, the brace system (brace system 670 and the like) can communicate with the computer system 700 using a controller such as controller 675. In some embodiments, the controller 675 can act as an internet transmitter / receiver that coordinates and routes data between the brace and the computer system 700. In some embodiments, the system 700 comprises a controller 675. In some embodiments of the invention, the computer system 700 can be configured to receive and / or transmit information to the brace system 670 (eg, a computer system in the user's home). Can be. In some embodiments, the computer system 700 may include a bus 701 for communicating information between components within the computer system 700. Further, in some embodiments, at least one processor 702 can be coupled to bus 701 to execute software code or instructions and process information. In some embodiments of the invention, the computer system 700 further comprises a main memory 704 that can be implemented using random access memory (RAM) and / or other random memory storage devices. In some embodiments, the main memory 704 can be coupled to the bus 701 to store information and instructions executed by the processor 702. Further, in some embodiments, the main memory 704 can also be used to store temporary variables, NMES program parameters, or other intermediate information during instruction execution by processor 702. .. In some embodiments, the computer system 700 also has a read-only memory (ROM) and / or other static storage device coupled to the bus 701 to store static information and instructions about the processor 702. Can include. In some embodiments of the invention, the computer system 700 may include one or more peripheral components that allow user interaction with the system 700. For example, in some embodiments, the system 700 moves the cursor over a conventional mouse, touch mouse, trackball, trackpad, or to communicate direction information and command selection to processor 702 and on display 721. Cursor control devices 723, such as other types of cursor direction keys for control, can be included. Further, the system 700 also has at least one keyboard 722 for facilitating data entry and commands and control of various aspects of the system 700, and at least one operably coupled to the processor 702 by bus 701. One communication device 725 can be included.

In some embodiments, any of the brace systems or assemblies described herein (including the brace system 670) receives and / or transmits information to the brace system and any coupled computer system. Information can be transferred from and / or to a computer system that is configured to do so. Looking at FIG. 5, in some embodiments, the computer system 800 can include a back-end system that can be used as a host computer for storing information measured and transmitted by the brace system. In some embodiments of the invention, the information refers to a computer system 700 (eg, a local computer system and / or controller that can be configured to receive and / or transmit information locally to a brace system). It can be used to receive and / or transmit between the brace system and the computer system 800. In some further embodiments, information can be received and / or transmitted directly between the brace system and the computer system 800 (eg, using portable wireless transmission). Further, in some embodiments, the brace can communicate with the computer system 800 and the computer system 700 using a controller such as controller 100. In some embodiments, the controller can act as an internet transmitter / receiver that coordinates and routes data between the brace and computer systems 700, 800.

In some embodiments of the invention, the system 800 may include at least one computing device that includes at least one or more processors 820. In some embodiments, some processors 820 may include processors 820 that reside within one or more conventional server platforms. In some embodiments, the system 800 can include a network interface 850a and an application interface 850b coupled to at least one processor 820 capable of running at least one operating system 840. Further, the system 800 may include a network interface 850a and an application interface 850b coupled to at least one processor 820 capable of processing one or more of the software modules 880 (eg, one or more enterprise applications). it can. In some embodiments, the software module 880 may include a server-based software platform. In some embodiments, the system 800 may also include at least one computer-readable medium 860. In some embodiments, the at least one computer-readable medium 860 can be coupled to at least one data storage device 870b and / or at least one data source 870a and / or at least one input / output device 870c.

In some embodiments, the invention can also be embodied as computer-readable code on a computer-readable medium 860. In some embodiments, the computer-readable medium 860 can be any data storage device capable of storing data, which data can then be read by a computer system. Examples of computer readable media 860 include hard drives, network attached storage, read-only memory, random access memory, flash-based memory, CD-ROMs, CD-Rs, CD-RWs, DVDs, magnetic tapes, other optical and non-optical. Includes an optical data storage device, or any other physical or material medium that can be used to tangibly store desired information, data, or instructions and is accessible by a computer or processor. Can be done.

In some embodiments, the computer-readable medium 860 can also be distributed across conventional computer networks. For example, in some embodiments, the computer-readable medium 860 can also be distributed across the network interface 850a and / or be accessible via it. In this case, the computer-readable code can be stored and executed in a distributed manner using the computer system 800. For example, in some embodiments, one or more components of the system 800 may be moored to transmit and / or receive data through a local area network (“LAN”) 890a. In some further embodiments, one or more components of System 800 can be moored to transmit or receive data through the Internet 890b (eg, wireless Internet). In some embodiments, at least one software module 880 running on at least one processor 820 can be configured to be coupled for communication through networks 890a, 890b.

In some embodiments, one or more components of the networks 890a, 890b may include one or more resources for data storage and retrieval. It can include any computer-readable medium in addition to the computer-readable medium 860, and can be used to facilitate the communication of information from one electronic device to another. Also, in some embodiments, the networks 890a, 890b are wide area networks (“WAN”), direct connections (eg, through a universal serial bus port), other forms of computer-readable medium 860, or any of them. Can include combinations of. In some embodiments, the software module 880 is configured to transmit and receive data from a database (eg, from a computer-readable medium 860 that includes a data source 870a and a data storage 870b that can configure the database). Can be done. Moreover, in some embodiments, the data can be accessed and received by the software module 880 from at least one other source.

In some embodiments, one or more components of the networks 890a, 890b can be worn, for example, a desktop computer, a personal computer including a laptop computer, an information terminal, a personal digital assistant, a mobile phone, a mobile phone, a smartphone, or the like. It can include several user-coupled devices 900 such as technology devices (eg smart watches, activity monitors, heart rate monitors), glasses, cameras, pages, digital tablets, and internet appliances, or other processor-based devices. .. In general, the client device can be any type of external or internal device such as a mouse, CD-ROM, DVD, keyboard, display, or other input or output device 870c. In some embodiments, at least one of the software modules 880 can be configured within the system 800 to output data to the user by at least one digital display. Further, in some embodiments, the various other forms of computer-readable medium 860 include routers, private or public networks, or other transmission devices or channels (both wired and wireless), coupled devices 900. Instructions can be transmitted or transmitted to a user interface such as.

In some embodiments, the described system 800 comprises one or more users 950 running on and from the software module 880 running on the system 800, and then to the system 800. , Data can be received, analyzed, entered, modified and transmitted. Some embodiments include having at least one user 950 access one or more modules, including at least one software module 880, through LAN 890a via fixed I / O device 870c. In some other embodiments, the system 800 can allow at least one user 950 to access the software module 880 via the Internet 890a or via a fixed or mobile I / O device 870c.

In some embodiments, the brace system or controller may include an upgradeable software module. In some embodiments, the software module can be upgraded by internet download (eg, through internet 890a shown in FIG. 5). In some embodiments of the invention, Internet downloads can include accessing at least one or more software modules stored in a cloud-based storage location. In some embodiments, the brace system may access a cloud-based storage location to perform periodic software updates and / or brace system data and / or data from the brace system controller and / or user. Data (ie, data from the brace system attached to the user) can be stored.

Considering the above embodiments, it is understood that some embodiments of the present invention can use various computer-implemented operations, including data stored in a computer system (such as the system 800 shown in FIG. 5). It should be. Further, in some embodiments, the above-mentioned application of the monitoring system can be stored on a computer-readable storage medium (computer-readable medium 860, etc.). These operations are operations that require a physical amount of physical manipulation. Usually, but not always, these quantities can be stored, transferred, combined, compared, and otherwise manipulated in the form, optical or magneto-optical of electrical, electromagnetic, or magnetic signals. Take the form.

Any of the actions described herein that form part of the present invention is a useful mechanical action. The present invention also relates to a device or device for carrying out these operations. An embodiment of the present invention can be defined as a machine that transforms data from one state to another. The data can represent articles that can be represented as electronic signals and electronically manipulated data. The transformed data can, in some cases, be visually rendered on the display to represent the physical object resulting from the data transformation. The transformed data can be stored in storage as a whole or in a specific format that allows the construction or depiction of physical and tangible objects. In some embodiments, the operation can be performed by one or more processors 820. In such an example, processor 820 can transform data from one thing to another. Furthermore, the method can be processed by one or more machines or processors that can be connected through the network. Each machine can convert data from one state or thing to another, also process the data, store the data in storage, send the data over the network, display the results, Alternatively, the results can be communicated to another machine. In addition, the described brace system has been manipulated, transformed, refined and refined so that the user or clinician can efficiently decompose into meaningful segments of data that can be made using medical-based decisions based on it. It will result in a large amount of data that must be reduced or changed from one state to another. In one embodiment, the brace system or controller comprises software that implements a data acquisition and pre-filtering algorithm, the algorithm satisfying some of the desired conditions (eg, the user wearing the brace). Movement is occurring above / below the desired threshold, or only when the ROM data is vertical to the user, or at regular time points throughout the day, such as once per minute. The data is stored on the storage medium only after it is captured (or during the user's awakening time, etc.). In another embodiment, the computer system 800 implements data reduction and pre-filtering functions. Computer-readable storage media (such as computer-readable media 860) as used herein refer to physical or tangible storage (as opposed to signals) and, without limitation, computer-readable instructions, data structures. Includes volatile and non-volatile, removable and non-removable storage media implemented in any method or technique for tangible storage of information such as, programming modules, or other data.

In some embodiments of the invention, the initiation of wireless data transfer from and / or to the brace system (eg, by using mobile transfer of data) is autonomous and / or semi-autonomous. It can be configured so that it does not require user configuration. For example, in some embodiments, the device can automatically check in when powered on. In some embodiments of the invention, the brace system can include a back-end system with one or more servers looking for a device to check in at a given time for configuration use. The back-end system is a recording system for patient compliance data. In some embodiments, if the device does not check in, the backend system or controller sends a message to the patient (or someone else on the contact list) indicating that the device should be checked in. can do.

Some embodiments of the invention can include uploading data to the backend by coupling to a smart device or computer. By way of example, in some embodiments, Bluetooth® products are used with any of the brace systems or assemblies described herein, as well as mobile computers, mobile phones, portable handheld devices, wearable techniques. It may provide a link between devices (eg, smartwatches, activity monitors, heart rate monitors, glasses, cameras, etc.), personal digital assistants (PDAs), tablets, and other mobile devices, as well as connectivity to the Internet. it can. In some embodiments, wireless transmission can be performed from the brace system to a smart device or computer via Bluetooth® radio signals. In some embodiments, a user interface screen can be used to allow device pairing by using the Bluetooth® protocol. In some further embodiments, uploading data to the backend can be done by binding to WiFi and connecting to the user's home or office network. In some embodiments, this will require the creation of a user interface screen that allows the user to select a wireless network to connect to and provide credentials to connect to that network.

In some embodiments of the invention, the brace system can utilize a radio protection scheme to control data access to and from the brace system. This can protect patient confidentiality and secure data. Some embodiments include protection against unauthorized radio access to device data and controls. In some embodiments, it is software that maintains the security of communications while avoiding the known drawbacks of existing older protocols (including, for example, Wired Equivalent Privacy (WEP)). Alternatively, it can include a hardware assisted protocol. In some embodiments, the usage data transmitted from the device (via Bluetooth, WiFi, or other means) is encrypted to ensure that only the patient or the patient's physician has access to this medical information. be able to. Encryption can be done by software running on the processor or by external hardware that processes the data before it is transmitted. In one embodiment, each set of logs is uniquely associated with the device that created the log. This can be done by the device tagging the data transmitted by the device with a unique identifier associated with the device. The unique identifier is set by the processor or by an external component of the system (eg, a UUID chip).

In some embodiments, wireless collection can include wireless collection of compliance data. For example, in some embodiments, brace system data, including the user's compliance with certain daily movements and / or one or more physiotherapy or exercise routines, can be monitored and recorded wirelessly. In some embodiments, the brace system can include wireless collection of compliance data and also includes making a record of all cases that the brace system sensor determines that the patient is wearing the brace system. be able to. In some embodiments, it can include stored data (eg, data previously measured by a brace system and stored in volatile or non-volatile memory). For example, this can include wireless collection of motion data, including data such as orientation data and acceleration data. In some embodiments, the brace system can continue to store and transmit data when the user is not wearing the brace system. In some embodiments, the data can be ignored, and in other embodiments, the data can be stored and / or transmitted wirelessly. In some embodiments, the brace system can wirelessly transmit data from the brace system to at least one remote medical system. In some embodiments, the brace system can wirelessly transmit data from the brace system to at least one physiotherapist and / or at least one physiotherapist system.

FIG. 6 shows a screen image 950 showing the current state of the brace assembly 960. In some embodiments of the invention, the brace system 951 is configured to project the state of the brace system 951 including the brace assembly 960 and display a display of the degree of bending and orientation of the brace assembly 960 with respect to the ground 965. Display screen 950 can be included. In some embodiments, the brace system 951 can render the display of the brace system 951 in substantially real time and also sensor data obtained from the brace assembly 960 (eg, usage tendency, muscle strength tendency, ROM). A graphical display or data related to (trends, etc.) can be displayed (see display portion 970 with trend data plot 975). In some embodiments of the invention, using one or more sensors, the brace system can communicate the position and movement of one or more sections of the brace system 951 in substantially real time. This information is processed by system 951 for representation on the display screen 950 and / or for communicating through a wired or wireless connection (eg, wireless data transfer between the knee brace assembly 670 and controller 675 shown in FIG. 3B). can do. In some embodiments, the data collected by the brace system 951 can allow healthcare professionals to adjust the brace system 951 based on this data. For example, the brace system 951 can measure muscle strength and / or range of motion of the knee surrounding the knee (eg obtained by an accelerometer or position encoder). The healthcare professional can then use this feedback and data to adjust the patient's treatment based on these readings and / or adjust the brace system 951.

In some embodiments, one or more brace control programs can be dynamic (eg, variable or variable, non-fixed frequency, non-fixed timing, non-fixed waveform, etc.) and also. One or more brace control programs that cause different types of EMS to be performed on different parts of the patient's body can be selected by the healthcare professional or patient. For example, feedback data obtained and rendered by the brace system 951 from the control electronics of the brace system shows that the patient's vastus medialis oblique muscle is stronger, but the patient's distal central hamstring (or another practice). If the morphology indicates that the patient's calf muscles) are not strengthened, a medical professional (eg, a doctor or physiotherapist) will perform a predetermined brace control program by one or more of these programs. The brace system 951 can be instructed. In some embodiments, the brace system 951 may include a specific program for the first week after surgery, a specific program for the first month after surgery, a specific program for arthritis, and the like. it can.

In some further embodiments, motion of any part of the brace assembly or system described herein can be detected. In some embodiments, at least one optical sensor or other type of sensor can be coupled or integrated with an assembly or system to detect motion and / or position. For example, FIG. 7 shows a display of a brace system 980 with motion data acquisition sensors 982, 984 according to some embodiments of the present invention. In some embodiments, one or more components of the brace assembly 986 can be monitored by sensors 982, 984. 8-9 provide a display of possible motion of various parts of the brace system that can be monitored in the brace system 950 shown in FIG. 7 (the brace system 980 indicates the brace system 950). In some embodiments, the optical sensor (eg, sensors 982, 984, etc.) can be used in combination with a portion of the brace system 980 that includes an optically identifiable area with an observed area. For example, in some embodiments, one or more optical sensors 982, 984 are for detecting motion in the vicinity of a brace system 980 comprising an observed region (ie, the region of the brace system detected by the optical sensor). Can be placed in. In some other embodiments, one or more photosensors 982, 984 can be arranged to detect motion relative to a region in the vicinity of a brace system that comprises an observed region (eg, including an observed region). The part of the brace system remains immobile, and the part of the brace system, including the optical sensor, can move relative to the observed area). In some embodiments of the invention, the observed area can include an optically reflective material. In some further embodiments, the observed area can comprise one or more markings that can be detected by one or more optical sensors. In some embodiments, the observed area can be provided with light emitting means. For example, in some embodiments, one or more of the observed areas may include light or infrared LEDs. For example, in some embodiments, the position and / or movement of the stay 987 can be monitored by the sensor 982. In some embodiments, the sensor 982 can include an optical sensor and the stay 987 can include an optical encoder 987a (eg, a tab or mark that can be read or detected by the sensor 982). Further, in some embodiments, the position and / or movement of the stay 988 can be monitored by the sensor 984. In some embodiments, the sensor 984 may include an optical sensor, the stay 988 may include an optical encoder 988a (eg, a tab or mark that can be read or detected by the sensor 984).

In some other embodiments of the invention, electrical detection of motion of the brace system 950 can be used. For example, in some embodiments, the components of the brace system 950 (eg, hinges) include an electrical resistor and / or an electrical resistant portion that has an electrical resistance that changes as a portion of the brace system 950 moves. Can be done. For example, in some embodiments, the electrical resistance can start at a known value and increase as the degree of hinge openness increases.

In some embodiments, one or more of the sensors 982, 984 may include linear, angular, rotation based position sensors / encoders. Some embodiments of the invention are linear displacement sensors, which can be utilized on a hinge bar to include a linear displacement sensor that determines which length setting the patient has selected. In some embodiments, the position sensor has been used to determine which ROM stop, and the ROM limit has been compared to what should or should not be used, or an extension lockout. Can be used to determine if was applied as prescribed. In some other embodiments, either the brace system or assembly described herein (eg, brace system 950, etc.) determines joint strength or force / torque output and correlates with patient recovery. It can be equipped with a force sensor, a torque sensor, and / or a dynamometer that can be integrated for the purpose.

Traditional NMES uses a variety of dc, ac, two-phase waveforms to elicit a muscle response in human tissue. These can be voltage driven or current driven and can be open loop or closed loop, and the wave amplitude can be controlled directly by device settings. Electrical stimulation can also be used to reduce edema or swelling in the target tissue. FIG. 10 shows a sensor assembly 1000 for detecting surface edema by photodetection according to some embodiments of the present invention. In some embodiments, Assembly 1000 can be used to regulate closed-loop feedback for electrical stimulation treatment of edema. In some embodiments, the emitter / sensor assembly 1005 emits red light from one or more LEDs 1010 into the skin epidermis layer (1060) and dermis layer (1070) of the patient and one or more lights. A detector (eg, phototransistor 1020, etc.) can be used to detect the light signal or wavelength (1085) reflected posteriorly from the skin. In some embodiments, the assembly 1000 can optically determine the level of surface edema near the detector. Water has a characteristic light absorption that can be used to make this decision. In some embodiments, the output from this assembly 1000 is used in a closed-loop feedback manner to allow the electrical stimulation system to optimize the stimulation parameters to achieve the desired level of edema reduction. Can be done. Some embodiments include waveform adjustment by setting a maximum current to set the wave amplitude. In addition, in some embodiments, two separate feedback loops are used to regulate the wave (dynamically fluctuate both current and voltage), thereby maintaining constant power dissipation. .. The amplitude of the current and voltage waveforms can be changed, but the overall shape of the waveform cannot be changed. In some embodiments, the waveform is constructed on carrier pulses from about 30 Hz to about 100 Hz and can provide pulse blocks that are about 100 μs to about 10,000 μs wide. Some embodiments include a closed loop feedback mechanism. In some embodiments, the power supply can provide a high current low voltage power supply with multiple nested feedback loops that, when added, produce a time-approximate constant power system. In some embodiments, the power supply can maintain a constant power output by attempting to maintain, firstly, the current load of the system and secondly, the voltage load of the system. The power output becomes relatively constant when added over a predetermined period of time and can be based on the amplitude selected by the user in the user interface.

In some embodiments, feedback can be collected behind the feedback loop after the feedback loop has passed the user. Some embodiments include a control system configured to maintain a constant output from the system. In some embodiments, the system can be configured to maintain a constant output as it passes through the user. In some embodiments, the conductive properties of the user's tissue are altered during the process of NMES. In some embodiments of the invention, the brace system can include a feedback loop that compensates for tissue changes by attempting to keep the output constant. As the resistance increases, the system can induce more current to keep the power dissipation level constant in the system. In some embodiments, if the resistance exceeds a certain point, the voltage of the system will spike in an attempt to break through the high resistance element and allow current to flow.

Some embodiments of the invention can comprise a system for pain relief. In some embodiments, pain relief can be provided using electrical stimulation without the use of anesthetics. In some embodiments, the electrical stimulation can be provided by one or more electrical stimulators coupled to the user using the brace system. In some embodiments, the brace system can include at least one electrical stimulator configured to provide electrical stimulation that provides pain relief to the user. The nerve responsible for transmitting sharp pain sends out a signal burst encoded to return to the autonomic nervous system. The introduction of a constant signal can disrupt the coding of the pain signal and provide some degree of pain relief. Some embodiments of the invention are configured to allow the user to self-adjust the signal for maximum usefulness. In some embodiments, this can be achieved by varying the pulse amplitude, pulse width, and / or pulse duration. For example, FIG. 11 shows a system 1100 for non-anesthetic pain relief using electrical stimulation therapy that negates pain impulses according to some embodiments of the invention. In some embodiments of the invention, non-anesthetic pain relief can be provided using electrical stimulation that overrides the pain impulse. In some embodiments, the non-anesthetic pain relief system may include a control unit 1105 that is connected to the epidermis 1103 by electrodes 1110 and 1115 configured to provide current 1120 through nociceptor 1125 of user 1101. it can.

Some embodiments of the invention can include systems configured to obtain biological feedback. In some embodiments, biological feedback can be provided by one or more biological feedbacks that are bound to the user using a brace system. In some embodiments, one or more of the brace systems or assemblies described herein may comprise at least one biological feedback sensor configured to provide biological feedback from the user. it can. For example, in some embodiments, the human contact sensor shown in FIG. 2T can include one or more biological feedback sensors located within the inner region of the brace. In some embodiments, these sensors can be proximity or contact sensors capable of determining whether a device (eg, brace, etc.) is worn by the user. Further, for example, an electrical sensor can be included that determines the impedance between the sensors to determine if the device is attached to human skin. In some further embodiments, blood pressure sensors, blood oxygen level sensors, heart rate sensors, laser or ultrasonic based sensors for measuring tissue or fluid movement, interstitial fluid levels for determining hydration levels. Used by other sensors such as hydration sensors to measure, force or pressure sensors to measure muscle activity / response, electrocardiogram type sensors to measure muscle mobilization by electrical stimulation therapy or to measure the level of muscle fatigue can do. In some further embodiments, by measuring the user's hydration level, the system can adjust the electrical stimulation signal to be more optimized or less painful for the user, or more. It is possible to provide the user with feedback to drink a lot of liquid.

In some further embodiments, the biological feedback sensor can include one or more temperature sensors. In some embodiments, one or more temperature sensors can be coupled or integrated with the brace system and used to monitor temperatures in close proximity to the user. In some embodiments, one or more temperature sensors are used in combination with NMES treatment and can be used to detect temperatures in close proximity to the stimulating electrodes. In some embodiments of the invention, one or more temperature sensors can be used in combination with NMES treatment and can be used for feedback control. For example, in some embodiments, the brace system can include a closed loop feedback system that provides electrical muscle stimulation (EMS) to the joints of a human patient in response to feedback from the detected temperature. In some embodiments, the brace system is one or more sensors from the area of the NMES electrode that is in physical contact with the patient's skin and / or in contact with the patient's skin. It can include one or more sensors configured to detect and / or obtain information. For example, in some embodiments, one or more temperature sensors can be used to detect temperatures in close proximity to one or more NMES electrodes. In some embodiments, the brace system also includes a sensor (s) and a brace control electronic device in communication, forming a closed loop system by a combination of joint bracing and electromuscular stimulation (EMS). be able to. Further, in some embodiments, the brace control electronics are configured to receive one or more temperature measurements of the patient's skin and / or electrodes and current / voltage / on the skin based on temperature. It can be further configured to instruct the sensor to apply power. For example, NMES can be reduced or increased, at least in part, based on temperature measurements from one or more temperature electrodes. In some embodiments, NMES burns are used using one or more temperature sensors to detect temperatures in close proximity to one or more NMES electrodes (the detected temperatures are used to control NMES). Can be substantially reduced or eliminated. In some further embodiments, one or more temperature sensors that detect changes in the user's body temperature and / or body core temperature can be used to estimate the user's activity level or the presence of infection. ..

Some embodiments of the invention include a system for monitoring the presence or concentration of at least one chemical, biochemical marker, or other analyte. In some embodiments, the analyte can include spontaneous or synthetic compounds or molecules and / or metabolites. For example, in some embodiments, the brace system can include a blood oxygen sensor device configured to measure the oxygen concentration of the blood. In some embodiments, a brace system configured to have a blood oxygen monitor can allow assessment of blood retention and also such as deep vein thrombosis (DVT) and pulmonary embolism, peripheral edema, etc. It can be used to prevent other potentially fatal events. For example, an example of collecting biological feedback is shown in FIG. Some embodiments include a blood oxygen sensor 1200 coupled to a stimulus system that includes at least two electrodes 1205, 1210.

In some further embodiments, one or more of the brace systems or assemblies described herein are nicotine, nicotine metabolites, and / or stimulants, inhibitors, stimulants, synthetic narcotics, and anabolic steroids. Can include sensor devices configured to measure other drugs or drug metabolites, including. In some embodiments, at least one of the brace systems or assemblies described herein is configured to detect one or more of these substances in vivo and notify a healthcare professional. It can be equipped with a plurality of sensors. The reason is that these substances can affect the healing and rehabilitation process. In some other embodiments, the brace system can be configured to have a sensor that detects the user's current environment. For example, in some embodiments, nicotine from active or second-hand smoke is detected using one or more brace system chemical sensors to determine whether the user has smoked and / or high levels of tobacco. It can be used to determine if it has been exposed to smoke.

In some embodiments, any of the brace systems or assemblies described herein can include at least one sensor configured to measure a user's heart rate. For example, in some embodiments, at least one heart rate sensor can be used to determine if a patient is performing prescribed exercise and / or physiotherapy. In addition, in some embodiments, at least one heart rate sensor can be used to determine the user's overall activity level (used for healing and data correlation). In some additional embodiments, lung and / or respiratory sensors can be used to provide data for maximal oxygen uptake (VO ₂ max) calculations and provide additional data on activity levels. .. In some embodiments, the brace system can include at least one heart rate sensor integrated into a portion of the brace. In other embodiments, the brace system can include at least one heart rate sensor coupled to the brace and adjacent to or at a distance from the brace.

Some embodiments of the invention can comprise a non-invasive blood pressure sensor configured to measure arterial blood pressure continuously or intermittently. In some further embodiments, the user's heart rate can be measured in addition to measuring the user's blood pressure. In some embodiments, one or more of the brace systems or assemblies described herein can include at least one blood pressure sensor integrated into a portion of the brace. In other embodiments, the brace system can include at least one blood pressure sensor coupled to the brace and adjacent to or at a distance from the brace.

In some further embodiments of the invention, one or more of the brace systems or assemblies described herein measure an electromyogram sensor, strain gauge sensor, or strain continuously or intermittently. Other sensors configured as such can be provided. In some embodiments, these measurements can be used to assess exercise, bias, or quantifiable data of muscle growth, muscle contraction or force, torque, or pressure resulting from muscle contraction. Can be provided. Muscle contraction may be manifested voluntarily or involuntarily by electrical muscle stimulation. In some embodiments, the data collected from the EMG or strain gauge sensor is utilized in a closed-loop feedback control method to optimize / customize electrical stimulation parameters, thereby being most efficient for the patient. Or can provide the strongest muscle contraction. The data can also be utilized by healthcare providers to fine-tune the treatment program based on patient data taken from electromyographic or strain gauge sensors.

Some embodiments of the invention can include the brace system or assembly described herein that can include at least one smart electrode. For example, FIG. 13 shows a smart electrode 1300 according to some embodiments of the present invention. In some embodiments, at least one of the brace systems, assemblies, or methods described herein can include one or more smart electrodes 1300, one or more smart electrodes 1300 having electrodes. It can include temperature responsive color change pigments that can be used to determine if an overheated condition has been experienced. In some embodiments, temperature-responsive color changes can be used to determine if the electrode has been heated past a point that would result in dielectric breakdown of the electrode material. Deterioration of the stimulating electrode due to dielectric breakdown can result in unsafe electrodes due to changes in electrical properties, and this type of degraded electrode should not be used with respect to humans. In some embodiments, any change within the smart electrode 1300 can be used to signal whether the electrode is safe to use or whether the electrode should be replaced. In some embodiments, color change can also be used to indicate to the physiotherapist whether the electrodes have probably resulted in skin burns, or the temperature threshold at which skin burns can occur. It can allow the physiotherapist to choose an electrical stimulation setting that produces a lower energy output. Some embodiments of the smart electrode 1300 can include a conductive silicon layer 1310 containing one or more sensors 1320 containing a temperature sensitive color changing material mounted on a fabric substrate 1340. In addition, some embodiments include a transparent hydrogel layer 1330 that covers at least a portion of the conductive silicon layer. The transparent hydrogel layer 1330 is a sensor layer and can provide physical protection for the sensor layer, which is optically transparent to allow detection of one or more sensors. In some other embodiments, the conductive silicon layer 1310 may be replaced by an alternative conductive or semi-conductive layer, including PCB, HDMI, conductive glass layer, conductive polymer layer, ceramic layer and the like. it can. In some other embodiments, a light sensor or photodetector element can be included to detect a color change in the smart electrode. In some embodiments, this automation can be achieved by including a color detection sensor that is placed directly on and / or in close proximity to the electrode surface, where the color detection sensor is at least a portion of the electrode. Can be configured to monitor the color of. In some embodiments, the color sensor can be coupled to a controller to monitor changes in electrode color that indicate unsafe electrode operating conditions for human use. In some embodiments, the color sensor can be used by the system to identify a change and stop the output of the system after the change is detected. In addition, in some embodiments, color changes can be detected automatically and are used in a closed-loop feedback scheme to optimize electrical stimulation parameters, thereby causing excessive temperature and patient burns. May prevent that from happening during electrical stimulation.

In some embodiments of the invention, at least one of the brace systems or assemblies described herein can include at least one adaptive electrode. For example, FIGS. 14A-14C show adaptive electrodes 1400, 1425, 1450 according to some embodiments of the present invention. In some embodiments, adaptive electrodes can be placed on one or more muscles to provide stimulation. In some embodiments, the electrodes can include a flexible PCB layer (shown as layer 1450), a layer with an array of silicon pads (layer 1425), and a hydrogel layer (layer 1400). Some embodiments include electrode clusters that include a plurality of individual electrodes (eg, electrodes comprising layers 1400, 1425, 1450). In some embodiments of the invention, the brace system can be self-adjusting by allowing current to pass through a selected number or all of the electrodes. In some embodiments, the electrode selectivity can be an indicator that it is aligned with a muscle fiber or muscle movement point and can include a set with minimal power dissipation, greater conductor performance. Furthermore, by dividing the single electrode into an aggregate of electrodes, it is possible to provide an improved distribution of the current applied to the surface of the user's skin. In addition, modern electrodes have maximum current densities around the edges of their pads, and the use of adaptive electrodes described effectively tiles the electrodes and currents outside the hot zone and over a larger area. Can be distributed, thereby improving user comfort and preventing skin burns.

In some further embodiments of the invention, the brace system may include one or more electrodes, including a circuit board located at the electrodes. Some embodiments of the present invention include systems and methods for using SPI communication from the controller to communicate with the setting gate of the electrode site. In addition, the set gate can determine which section of the electrode produces an effective electrical stimulation signal. In some embodiments of the invention, one or more electrodes and / or an array of electrodes is such that a particular stimulation pattern introduces blood flow into the muscles of a given limb and into the tissue of that limb. Can include an arrangement of electrodes configured to contract in a pattern or reduce edema within the region.

Some embodiments of the invention include a brace system with an integral stimulus that is coupled to cold or hyperthermia. In some embodiments, the brace system can apply selective hyperthermia and cryotherapy, and the hyperthermia and cryotherapy can change the internal temperature of at least a portion of the brace within the brace. It can be delivered to the extremities. In some embodiments, this can be achieved in conjunction with applying the stimulus to the selected limbs. In some embodiments, heating and / or cooling can be applied to the entire inside of the brace or to selected locations inside the brace. In some embodiments, the brace system can include a solid heat exchanger that directly heats or cools a particular location or region inside the brace using the Peltier effect. Some embodiments of this system can use heat exchangers on the outside of the brace. For example, in some embodiments, a tube system of heat conductive material can circulate a fluid cooled by an external heat exchanger. In some further embodiments, the system can use phase change cooling material to provide cooling throughout the inside of the brace or to selected locations inside the brace. In some embodiments, the system can use a phase change cooling material that freezes at 58 ° F. (about 14.4 ° C.) and does not lower the temperature of the limb under treatment below safe levels.

Some embodiments of the present invention may comprise a brace system that provides mechanical manipulation of muscles to improve blood flow and / or prevent the formation of blood clots. Some embodiments of the present invention can use multiple air bladder to form concentric rings around a given limb. In some embodiments, if the pressure in these rings increases in a continuous ring aligned with each other, a peristaltic pumping action is introduced into the underlying tissue and blood into the tissue of a given limb. It is possible to bring about an increase in flow.

Some embodiments include a shoulder vest or sling with an integrated electrical stimulation electrode and an inflatable bolster, the inflatable bolster being utilized to improve contact, conductivity, and comfort with respect to the skin. Pressure can be applied to. In some embodiments, the expansion of the air bladder is selectively applied as a method of improving the contact pressure of the electrodes, is electronically controlled, and is comfortable for the user without mechanically rearranging the electrodes. Bring. In addition, in some embodiments, a pump and / or expansion gas and / or fluid system (eg, including a bladder) can be used for electrode compression. In addition, in some embodiments, the inflatable bolster can be utilized to increase or decrease pressure on specific tissues for the comfort of the patient during exercise, sleep, or other activity. For example, an inflatable bolster can be applied posterior to the shoulder joint complex during sleep and manually inflated by the user to provide pain relief and comfort while sleeping.

Some embodiments include a brace system with an integrated pressure therapy system. For example, in some embodiments, an integrated pressure therapy system can be used to treat deep vein thrombosis as well as perform general compression therapy. For example, in some embodiments, the brace system can function as a pressure therapy system using an inflatable bolster or bladder in combination with selectively applied and electronically controlled operation. In some embodiments, the pressure therapy system can be combined with an electrical stimulation electrode and system to provide a comprehensive tissue treatment system. Further, in some embodiments, the pressure therapy system can be combined with an electrical stimulation system and combined with the application of heat / ice temperature therapy to provide a comprehensive tissue treatment system.

Figures 15-22 show oscilloscope scan data of NMES under various stimulation conditions generated using at least one of the brace systems or assemblies described herein. For example, referring first to FIG. 15 showing the NMES postoperative oscilloscope scan 1500 of the pulse train, the scan shows a pulse train view with a pulse train duration of 3 seconds, a working cycle of 13 seconds on / 10 seconds off, and a vertical of 20 V. It is a division and a horizontal division of 5 seconds. The exemplary electrical stimulation pulse is a single-phase pulse at a rate of about 50 pulses / sec with a 5 ms pulse width and a 25% duty cycle, with a power level set to 100 on the device under a 500 ohm load. As illustrated, the pulse trains oscillate between channels (eg, muscle groups) over a predetermined period of time and do not overlap. In some embodiments, the pulse train is an extension of 3 seconds to regain motivation and allow the patient to better coordinate voluntary contractions with electrically stimulated contractions.

FIG. 16 shows the NMES post-operative oscilloscope scan 1600 of individual pulses of the channel according to some embodiments of the invention, waveforms of 20 V vertical section and 5 ms (hereinafter “ms”) horizontal section Show the view. The single-phase pulse was applied at a rate of about 50 pulses / sec with a 5 ms pulse width and a 25% duty cycle, and the device power level was set to 100 under a 500 ohm load. The illustrated waveform is not a standard square, sine, triangle, sawtooth, or other waveform and is therefore not a typical waveform seen during electrical stimulation. The illustrated waveform is a complex waveform, which has a high voltage spike on the front end, which rapidly transitions to the low voltage saddle, followed by towards the end of the pulse. Accompanied by an increase in voltage. The waveform indicates the closed-loop feedback power control used by the system, as it responds quickly to the desired power delivery and current flow for the device configuration. Compared to traditional NMES electrical stimulation parameters, the voltage is much lower and the pulse width is much longer. FIG. 16 shows electrical stimulation pulses targeting the vastus medialis plagiocephalic (VMO) muscle group. FIG. 17 shows a scan 1700 with a waveform that is similar to FIG. 16 and targets the rectus femoris (RF) group. In some embodiments, this waveform is identical to VMO, but in other embodiments, this waveform is modified and differs for optimal stimulation of both muscle groups.

FIG. 18 shows the NMES intensity osloscope scan 1800 of the pulse train according to some embodiments of the present invention. Scan 1800 shows a pulse train view showing a 1 second pulse train duration with a working cycle of 12 seconds on / 10 seconds off. The vertical division is 20V and the horizontal division is 5 seconds. The view is a single-phase pulse at a rate of 50 pulses / sec with a 5 ms pulse width and a 25% duty cycle, and the device power level is set to 100 under a 500 ohm load. As seen in osloscope scans, the pulse trains oscillate between channels (eg, muscle groups) over a predetermined period of time and do not overlap. The 1 second pulse train allows for a sustained contraction time similar to the contraction length that the patient will experience during exercise.

FIG. 19 shows a scan 1900 with a view of the electrical stimulation pulse waveform with a vertical section of 20 V and a horizontal section of 5 ms. Scan 1900 is a single-phase pulse at a rate of 50 pulses / sec with a 5 ms pulse width and a 25% duty cycle, with the device power level set to 100 under a 500 ohm load. The illustrated waveform is not a standard square, sine, triangle, sawtooth, or other waveform and is therefore not a typical waveform seen during electrical stimulation. The illustrated waveform is a complex waveform, which has a high voltage spike on the front end, which rapidly transitions to the low voltage saddle, followed by towards the end of the pulse. Accompanied by an increase in voltage. The waveform indicates the closed-loop feedback power control used by the system, as it responds quickly to the desired power delivery and current flow for the device configuration. Compared to traditional NMES electrical stimulation parameters, the voltage is much lower and the pulse width is much longer. FIG. 19 shows electrical stimulation pulses targeting the vastus medialis plagiocephalic (VMO) muscle group. FIG. 20 shows a scan 1900 with a waveform targeting the rectus femoris (RF) group, similar to FIG. In some embodiments, this waveform is identical to VMO, but in other embodiments, this waveform is modified and differs for optimal stimulation of both muscle groups.

FIG. 21 shows a TENS intensity osloscope scan 2100 of a pulse train according to some embodiments of the present invention. FIG. 21 shows a pulse train view with a vertical section of 20 V and a horizontal section of 10 ms. The electrical stimulation pulse is a biphasic symmetric pulse at a rate of 100 pulses / sec with a 1 ms pulse width and a 20% duty cycle, with the device power level set to 50 under a 500 ohm load.

FIG. 22 shows a TENS intensity osloscope scan 2200 of individual pulses according to some embodiments of the present invention. This figure shows a view of the electrical stimulation pulse waveform with a vertical section of 20 V and a horizontal section of 2.5 ms. The electrical stimulation pulse is a biphasic symmetric pulse at a rate of 100 pulses / sec with a 1 ms pulse width and a 20% duty cycle, with the device power level set to 50 under a 500 ohm load. The illustrated waveform is not a standard square, sine, triangle, sawtooth, or other waveform and is therefore not a typical waveform seen during electrical stimulation. The illustrated waveform is a complex waveform, the complex waveform having a high voltage spike on the front end, the high voltage spike rapidly transitioning to a low voltage ramp down at the end of the pulse. The waveform indicates the closed-loop feedback power control used by the system, as it responds quickly to the desired power delivery and current flow for the device configuration. Compared to traditional TENS electrical stimulation parameters, the voltage is much lower and the pulse width is much longer.

As mentioned earlier, some embodiments of the invention can include a brace system or assembly that includes a controller 675 that is coupled to a computer system or device such as a personal computer and / or smartphone. When coupled to a treatment control system, one or more functions and / or modes of operation of the wearer's brace system or assembly are controlled and monitored through a graphical user interface (“GUI”) using a computer system or device. be able to. For example, FIG. 23 shows a display 2300 of a treatment system control GUI with some of the systems of the invention. In some embodiments, the display 2300 allows the user to combine, pair, or synchronize and / or register the brace assembly for use, and / or confirm help information. An introductory and start menu that encourages and enables, and can include an introductory and start menu that includes text, audio, video, and / or other media files. In addition, the display 2300 may select one or more selectable actions from which the user may select to combine, pair and / or register the brace assembly, or to access help information. Can include steps. For example, in some embodiments, step 2310 sends audio information (eg, verbal instructions) to a sound generator for display on the GUI and / or coupled to the user's computer system or device. To initiate the sending of help information for, a "find barcode" selection means that the user can optionally select can be included. In some further embodiments, step 2320 can be used to select an in-application scanner to scan and synchronize a brace or brace assembly with garment. In some further embodiments, step 2330 can be used to add additional documentation to the system and related applications. In other embodiments, alternative optional steps or processes can be used in place of steps 2310, 2320, 2330, and / or include additional optional optional steps. Can be done.

In some embodiments, if the user selects step 2310, the media window can display instructions for the location of the barcode. For example, FIG. 24 shows a display 2400 of a therapeutic system control GUI according to some embodiments of the present invention. In some embodiments, the display 2400 can include a media window 2410, which can display information related to the position of the garment barcode within the media window 2410. The information can include text, graphics, video, still images, or a combination thereof. In some embodiments, audio information can be displayed in place of or in addition to text, graphics, video, still images, or a combination thereof.

In some embodiments of the invention, the user can download the treatment control application to a wireless device (eg, mobile phone, smartphone, etc.). In some embodiments, the user can set up a profile and then pair the application to the user's brace and use the user's GUI to initiate stimulation and / or range of motion treatment. Can be done. For example, in some embodiments of the invention, the GUI of the user can be used to initiate Bluetooth support pairing or coupling of one or more components of a treatment control system. Can be or can be monitored. FIG. 25 shows one embodiment of the display 2500 of the treatment system control GUI according to some embodiments of the present invention. In some embodiments, the display 2500 may include at least one indicator 2510 that indicates or indicates the state of synchronization with the user's garment. In some embodiments, the display 2500 can include step 2520, which allows the user to activate Bluetooth. Further, in some embodiments, step 2530 can be used to synchronize with a mobile device.

FIG. 26 shows a display 2600 of a treatment system control GUI according to some embodiments of the present invention. In some embodiments, the display 2600 can include a media window 2610, within which information related to Bluetooth® synchronization can be displayed. The information can include text, graphics, video, still images, or a combination thereof. In some embodiments, audio information can be displayed in place of or in addition to text, graphics, video, still images, or a combination thereof.

FIG. 27 shows a display 2700 of a treatment system control GUI according to some embodiments of the present invention. In some embodiments, the display 2700 can include a visual icon 2710 that encourages the user to pair the user's garment with the user's device using the selector bar 2720. In some embodiments, the information bar 2730 can display the state of the Bluetooth® binding that is bound between the user's garment and the device. In addition, FIG. 28 shows a display 2800 of a therapeutic system control GUI according to some embodiments of the present invention. In some embodiments, the display 2800 can include an information bar 2810 indicating an error connection.

In some embodiments of the invention, the GUI can provide guidance for using garments. For example, FIG. 29 shows a display 2900 of a therapeutic system control GUI according to some embodiments of the present invention. In some embodiments, the information display 2910 can contact the user for help in wearing the garment. In addition, the associated visual icon 2920 can provide a display of the garment where the user may need assistance or guidance regarding wearing it, and the selection bar 2930 gives the user access to any help display. I will provide a. For example, FIG. 30 shows a display 3000 of a treatment system control GUI according to some embodiments of the present invention. In some embodiments, the display 3000 can include an information bar 3010 having one or more instructions, and the information segment 3030 can include mounting instructions. Further, the visual indicator 3020 includes a visual display of text, graphics, video, still images, or a combination thereof, and can show or illustrate one or more steps of the garment wearing procedure. In some embodiments, audio information can be played in place of or in addition to text, graphics, video, still images, or a combination thereof.

In some embodiments, the selection bar 3040 is used to exit help or proceed to another help step or topic. For example, FIG. 31 shows a display 3100 of a treatment system control GUI according to some embodiments of the present invention. In some embodiments, the display 3100 can include an information bar 3110 that provides help for aligning the electrodes. In addition, the visual indicator 3120 includes a visual display of text, graphics, video, still images, or a combination thereof, and can show or illustrate one or more steps of a fitting procedure for aligning electrodes. In some embodiments, audio information can be played in place of or in addition to text, graphics, video, still images, or a combination thereof.

FIG. 32 shows a display 3200 of a treatment system control GUI according to some embodiments of the present invention. In some embodiments, the display 3200 can include an information bar 3210 that provides help for fastening the brace straps. Further, the visual indicator 3220 includes a visual display of text, graphics, video, still images, or a combination thereof, and can indicate or illustrate one or more steps of the wearing procedure for fastening the brace strap. In some embodiments, audio information can be played in place of or in addition to text, graphics, video, still images, or a combination thereof.

FIG. 33 shows a display 3300 of a treatment system control GUI according to some embodiments of the present invention. In some embodiments, the display 3300 may include an information bar 3310 indicating instructions for inserting a garment controller. Further, the visual indicator 3320 includes a visual display of text, graphics, video, still images, or a combination thereof, and can indicate or illustrate one or more steps of inserting a garment controller. In some embodiments, audio information can be played in place of or in addition to text, graphics, video, still images, or a combination thereof.

In some embodiments, the GUI can be used to activate the garment. For example, FIG. 34 shows a display 3400 of a therapeutic system control GUI according to some embodiments of the present invention. In some embodiments, the display 3400 can include information or an action bar 3410 that informs the garment-activated stomach. In some embodiments, the information segment 3420 can include instructions or information related to the garment activation state or procedure. In some embodiments, the visual indicator 3425 can include an example of a garment requesting activation, and the action selection 3430 can include a test garment action icon 3430.

The GUI of the present invention can allow the user to test the garment in some embodiments. For example, FIG. 35 shows a display 3500 of a therapeutic system control GUI according to some embodiments of the present invention. In some embodiments, the display 3500 can include information related to the state of various aspects of the user's garment. For example, in some embodiments, the function 3515 may include an indicator 3515a associated with a Bluetooth® connection state. In addition, the function 3520 may include an indicator 3520a associated with the connection of the controller. Display portions 3600 and 3650 shown in FIG. 36 show different Bluetooth® states and connection states. For example, the display portion 3600 includes a state 3610 indicating that the Bluetooth® connection is being processed, and the display portion 3650 includes a state 3625 indicating that the controller connection is being processed.

FIG. 37 shows a display 3700 of a treatment system control GUI according to some embodiments of the present invention. In some embodiments, the display 3700 may include a help icon 3710 that allows the user to access one or more help information sections (eg, as described above). The display 3700 can also include an access bar 3725 that includes various functions or access icons. For example, the home icon 3750 can be used to direct to the GUI home page. In addition, the stimulator icon 3760 or range of motion icon 3770 can be used by the user to select a treatment. For example, the stimulator icon 3760 can be used to access one or more functions or states of the stimulator combined or integrated with the user's garment, and the range of motion icon 3770 is used to the wearer Procedures designed to increase range of motion can be initiated. In addition, the menu icon 3780 can allow the user to access further goals and application preferences.

In some embodiments, the GUI can make it possible to set goals for treatment. For example, FIG. 38 shows a display portion 3800 of a therapeutic system control GUI according to some embodiments of the present invention. In some embodiments, the display 3800 can include a set stimulus target section 3825 that includes a target section 3810, a range of motion target section 3827. In some embodiments, the target section 3910 can include one or more icons that reference the treatment site. For example, the icon 3815 can include a reference to a knee procedure and the icon 3820 can include a reference to a shoulder procedure. In some embodiments, the set stimulus goal 3825 section may include advice relating to the goal and the interests of the goal, including the procedure to be advised. In some embodiments, the range of motion target 3827 can include a date selector 3830 configured to allow the user to select a treatment date. In some embodiments, the exercise setting display 3832 can include a movable indicator 3832a for setting a user's target goal associated with a body part displayed as an icon 3834. For example, with reference to a goal related to the user's selection of the knee treatment icon 3815, the exercise setting display 3832 can include a movable indicator 3832a for setting the user's desired target extension angle. Further, the exercise setting display 3836 can include a movable indicator 3836a for setting a user's target target associated with the body part displayed as the icon 3838. In this example, the motion setting display 3836 can include a movable indicator 3836a for setting the user's desired target flexion angle. In addition, FIG. 39 shows a display portion 3900 of a treatment system control GUI according to some embodiments of the present invention. In some embodiments, the display 3900 can include an information chart 3850 with goals selected by the user, including goals as a function of dates selected by data selection 3830. For example, in some embodiments, user-defined flexion, extension, and range of motion goals can be displayed as a function of date.

Some embodiments allow the user to increase the number of goals. For example, in some embodiments, the pain reduction goal section 3860 can be used to set a target pain reduction goal. In some embodiments, this can be set as a function of dates defined using data selection 3860a. In some embodiments, a pain gauge 3870 is used and a movable indicator 3782 can be used to set a target level of pain. In addition, the pain gauge 3870 can include multiple icons 3875 indicating pain levels from no pain to moderate pain to worst pain. Further, in some embodiments, the action indicator 3878 can be used to add a goal and the action selection 3890 can be used to set a goal. In some embodiments, the display 3879 can include a target display that is displayed as a function of date 3880 and pain level 3885. At any time, the access bar 3892 can be provided to allow the user to access other features of the system.

FIG. 40 shows a display portion 4000 of a treatment system control GUI according to some embodiments of the present invention. In some embodiments, the display 4000 can include a drop-down menu 4010 configured to select a date range, FIG. 41 shows the correspondence of the treatment system control GUI according to some embodiments of the present invention. The display portion 4100 to be used is shown.

FIG. 42 shows a display portion 4200 of a treatment system control GUI according to some embodiments of the present invention. In some embodiments, the display 4200 may include a selection 4220 configured to allow the user to switch between goal and achievement. In some embodiments, the icon 4230 can display one or more body parts associated with a goal or achievement, and the goal and achievement display 4240 is a treatment type 4260 and date 4270 (eg, daily goal). As a function of (1 week goal, and / or 1 month goal, etc.), a display of target goal 4245 vs. actual achievement 4250 can be included. In some embodiments, the goal and achievement display 4240 can be configured as a goal and achievement display 4340 having a one-day comparison of goals and achievements (see, eg, FIG. 43 and display portion 4300). FIG. 44 shows the display portion 4400 of the treatment system control GUI according to some embodiments of the present invention and displays a monthly version of the goal and achievement display 4240 (shown as the goal and achievement display 4440).

FIG. 45 shows a display portion 4500 of a treatment system control GUI according to some embodiments of the present invention. In some embodiments, the display portion 4500 may comprise an achievement display 4510 (having a selector toggle 4505 set to achieve), wherein the award section 4515 is directed to a specific or non-specific goal. It can include one or more achievement awards based on the user reaching or exceeding. Award section 4515 can include awards for stimulus goals. FIG. 46 shows a display portion 4600 of a therapeutic system control GUI according to some embodiments of the present invention, for flexion-related awards (award display 4610), extension-related awards (award display 4620), and range of motion. The relevant awards (award display 4630) are shown. FIG. 47 shows the display portion 4700 of the treatment system control GUI according to some embodiments of the present invention, including an award display 4715 with the award 4720, and FIG. 48 shows the treatment according to some embodiments of the present invention. It shows the display portion 4800 of the system control GUI and includes the award display 4810, the award display 4820, and the award display 4830. FIG. 49 shows a display portion 4900 of a treatment system control GUI according to some embodiments of the present invention, including an award display 4915 having an award 4918, and FIG. 50 shows treatment system control according to some embodiments of the present invention. A display portion 5000 of the GUI is shown, showing an award display 5015, an award display 5020, and an award display 5025.

FIG. 51 shows a display 5100 of a treatment system control GUI according to some embodiments of the present invention. In some embodiments, the display 5100 may include a notification or information display 5110 configured to display the therapeutic status (eg, the number of completed stimuli, etc.). In some embodiments, the award indicator 5120 can display based on the display treatment status.

FIG. 52 shows a display 5200 of a treatment system control GUI according to some embodiments of the present invention. In some embodiments, the display 5200 can be displayed based on the user's choice of access bar 3725. In some embodiments, the display 5200 may include a help icon 5210 that allows the user to access one or more help menus. The display 5200 may also include a garment selector 5220, which can be optionally selected by the user to add additional garment to the stimulation session. Further, in some embodiments, the battery indicator 5230 can be used to indicate the battery charge of the user's device. Stimulation pulse activity can also be monitored. For example, FIG. 53 shows a display 5300 of a treatment system control GUI according to some embodiments of the present invention. In some embodiments, the display 5300 may include a pulse current indicator 5310 and / or a pulse level indicator 5320.

FIG. 54 shows a display 5400 of a treatment system control GUI according to some embodiments of the present invention. In some embodiments, the display 5400 can include a timer 5410 capable of displaying the time remaining in the treatment session. In addition, some embodiments include a pause selection 5420 configured to allow the user to pause the treatment session.

In some embodiments, the GUI can be configured to have different help menus that allow the user to select from different help topics. For example, FIG. 55 shows a display 5500 of a therapeutic system control GUI according to some embodiments of the present invention. In some embodiments, the display 5500 can include a dashboard help section 5510 that includes a menu 5525 that allows the user to select one or more help subjects. In addition, FIG. 56 shows a display 5600 of a therapeutic system control GUI according to some embodiments of the present invention. In some embodiments, the display 5600 can include a PIN management help section 5610 that can include a menu 5620 configured to have selectable topics related to PIN management.

FIG. 57 shows a display 5700 of a treatment system control GUI according to some embodiments of the present invention. In some embodiments, the display 5700 can include a menu 5710 configured to have selectable preferences. In addition, FIG. 58 shows a display 5800 of a therapeutic system control GUI according to some embodiments of the present invention. In some embodiments, the display 5800 can include a menu 5810 configured to have a user-selectable profile help topic. FIG. 59 shows a display 5900 of a treatment system control GUI according to some embodiments of the present invention. In some embodiments, the display 5900 may include a topic title 5910, and the menu 5920 may include one or more questions related to that topic. The visual window 5930 includes a visual overview of the treatment, and the information segment 5940 can contain instructions, advice, or other information related to the treatment. In addition, FIG. 60 shows a display 6000 of a treatment system control GUI according to some embodiments of the present invention. In some embodiments, the display 6000 can include a range of motion test help 6010 that includes a menu 6020 configured to select at least one help topic.

FIG. 61 shows a display 6100 of a treatment system control GUI according to some embodiments of the present invention. In some embodiments, the display 6100 may include a range of motion help 6110 that includes a menu 6120 that includes one or more selectable help topics. In addition, FIG. 62 shows a display 6200 of a therapeutic system control GUI according to some embodiments of the present invention. In some embodiments, the display 6200 can include a resting stimulus help 6210 that includes a menu 6220 containing one or more help topics related to the stimulus. In addition, FIG. 63 shows a display 6300 of a treatment system control GUI according to some embodiments of the present invention. In some embodiments, the display 6300 can include a resting stimulus help 6325 including a menu 6330 containing one or more help topics related to the stimulus.

FIG. 64 shows a portion of the stimulation circuit 6400 of a treatment control system according to some embodiments of the present invention. In some embodiments, the circuit 6400 may include at least one resistor 6450 coupled in parallel with at least one capacitor 6460 coupled to ground. In some embodiments, this configuration allows a comfortable stimulation pulse when delivered to the wearer.

FIG. 65A shows a display 6500 of a treatment control system according to some embodiments of the present invention. In some embodiments, the display 6500 allows the user to enter and / or review personal information, including, but not limited to, height, weight, birthday, and gender within the information window 6510. Can be done. In addition, FIG. 65B shows a display 6550 of a treatment control system according to some embodiments of the present invention. In some embodiments, the display 6550 may include an information window 6560 that includes at least a portion of the user's health information. For example, in some embodiments, certain information may include information about the immediate surgery associated with the current or pending treatment provided by the treatment control system.

In some embodiments, the user can select a garment type and initiate a connection to the garment. For example, FIG. 66 shows a display 6600 of a treatment control system according to some embodiments of the present invention. In some embodiments, the display 6600 can include a garment type 6610 from which the user can select and add one or more garments for use in one or more treatment sessions. Using the Bluetooth® connection 6620, the user can connect to one or more garments to initiate a treatment session. In addition, FIG. 67 shows the display 6700 of the treatment control system including the scroll portion of the display 6600 showing the background information window 6710. In some embodiments, the user can scroll through information window 6710 to access different parts of window 6710.

In some embodiments, the user can use the dashboard to monitor and track treatment sessions. For example, FIG. 68 shows a display 6800 of a treatment control system that includes a dashboard 6810. In this example focused on knee treatment, the progress bar 6820 includes the number and type of treatment sessions completed or in progress and / or the state of treatment including the number and type of treatment sessions pending or planned. be able to. Further, in some embodiments, one or more access tabs allow the user to access various treatment sessions or programs, session or program settings, or data recorded during any session or program. Can be. For example, some embodiments include a stimulation tab 6830 and / or a ROM / flexion / extension tab 6840, a pain indicator tab 6850, and a step indicator tab 6860.

Some embodiments include a display of treatment settings that can be configured or reconfigured by the user. FIG. 69 shows a display 6900 of a treatment control system according to some embodiments of the present invention. In some embodiments, the display 6900 can include a treatment session window 6910 that includes one or more treatment settings or controls. For example, some embodiments include a thigh dial 6920 and / or a knee dial 6930 and / or a site 3 dial 6940 and / or a site 4 dial 6950. In some embodiments, any of the dials 6920, 6930, 6940, 6950 provides controls that allow the user to increase or decrease one or more therapeutic parameters indicated by the dials 6920, 6930, 6940, 6950. Can include.

Some embodiments may include a visual or graphical display during the treatment session. For example, FIG. 70 shows a display 7000 of a treatment control system according to some embodiments of the present invention. In some embodiments, the display 7000 can include a visual guide 7010 that provides an anatomical display of a portion of the body of the user being treated. In some embodiments, the visual guide 7010 can include therapeutic parameters 7020 from the user, including flexion and / or extension and / or range of motion data. In some further embodiments, the therapeutic parameter 7020 can be tracked and plotted over a predetermined period of time. For example, FIG. 71 shows a display 7100 of a treatment control system according to some embodiments of the present invention. In some embodiments, the display 7100 can include a treatment progression plot 7110 showing flexion and / or extension and / or range of motion data plotted as a function of time. Further, in some embodiments, detail section 7120 may include tabular data of flexion and / or extension and / or range of motion data alongside pain data. With reference to FIG. 72, some further embodiments include a display 7200 showing the progression of which the treatment progression plot 7210 is represented as average power. The display 7200 can also include a treatment date section 7220 that allows the user to view the plot 7210 with the selected data range. In addition, session detail section 7230 can include tabular session data including start time and end locations of treatment sessions and average power from the session.

In some embodiments, the user can monitor pain based on timing, session activity, or other desired parameters. For example, FIG. 73 shows a display 7300 of a treatment control system according to some embodiments of the present invention. In some embodiments, the display 7300 can include a therapeutic pain plot 7305 that includes pre-session pain and / or post-session pain and / or average daily pain level. In addition, session detail section 7310 can include tabular pain data as a function of session date.

In some other embodiments of the invention, the user's steps can be monitored and displayed. For example, FIG. 74 shows a display 7400 of a treatment control system according to some embodiments of the present invention. In some embodiments, the display 7400 includes a therapeutic step plot 7405 that includes steps as a function of time, and session detail section 7410 can provide tabular steps as a function of dates.

As mentioned earlier with respect to FIGS. 3A and 3B, some embodiments include various electronic components that can be integrated into one or more modules of the brace system, the modules of which vary. It can be combined or recombined to form a configuration. For example, FIG. 75 shows a garment 7510, a therapeutic system 7500 comprising a garment 7510, including a controller 7520 integrated or coupled to the garment 7510. In addition, some embodiments include one or more sensor pods 7525 integrated or coupled to the garment 7510. In some embodiments, the controller 7520 includes a rechargeable power storage. Moreover, in some embodiments, the sensor pod comprises onboard power.

In some embodiments, one or more sensor pods 7525 can be connected to controller 7520 using a wired or wireless connection. For example, in some embodiments, one or more sensor pods 7525 can be connected to controller 7520 using a Bluetooth® wireless connection. In some embodiments, one or more of the sensor pods 7525 can exchange data with the controller 7520, which exchanges data or related data with the user's device, such as the mobile device 7530. Can be done. Further, in some embodiments, the mobile device 7530 can exchange data or related data with an external server system 7540 (eg, cloud server and / or storage system). In some embodiments, the controller 7520 can be configured to exchange information with one or more of the sensor pod 7525 and the mobile device 7530 at substantially the same time. Referring to FIG. 76 showing data type 7600 for the treatment system of FIG. 75 according to some embodiments of the invention, in some embodiments the exchanged data are stimulation data 7610 and / or range data 7630. And / or pain data 7660 and / or activity level data 7690 can be included. In some embodiments, the stimulus data 7610 may include information or data from one or more treatment sessions and / or treatment power levels and / or power level changes and / or treatment types and / or stimulus comfort. it can. In some embodiments, the range of motion data 7630 may include range of motion and / or flexion and / or extension information or data once a day (or a predetermined number of times over other times). In some embodiments, this data can enable passive monitoring and gait analysis. In some further embodiments, the pain data 7660 can include pre-stimulation and post-stimulation pain levels that are measured and / or distributed at least 3 times on a daily basis or over other periods. In some other embodiments, the activity level data 7690 can include step number, acceleration, and velocity data.

Some embodiments of the present invention use one or more ROMs, accelerometers, gyroscopes, and EMGs to analyze activity level data 7690 including the gait phase. Such gait analysis can better assess rehabilitation and / or training progress by comparing post-injury or post-training data with pre-injury, pre-treatment, or pre-training baseline data. Gait analysis can also be used alone or in conjunction with other biometric analyzes to identify patients in some embodiments.

In some embodiments, EMG signal and force relationship analysis can also be useful in assessing rehabilitation and training progress. Some embodiments provide customized treatment and / or training based on feedback from the gait phase or EMG signal and force analysis. In some embodiments, the EMG signal can be evaluated alternating with stimulation therapy. In some other embodiments, the EMG signal is evaluated at the same time as stimulation therapy using conventional signal filtering and analysis techniques. Finally, in some embodiments, surface EMG analysis can be used to diagnose muscle and / or neurological disease characteristics.

FIG. 77 shows data categories 7700 exchanged and stored within the components of the therapeutic system of FIG. 75 according to some embodiments of the present invention. For example, some embodiments are exchanged between servers, such as when the mobile device 7530 is capable of exchanging data or related data with an external server system 7540 (eg, cloud server and / or storage system). And / or includes server data category 7710 containing data or information stored on the server. Some embodiments also include mobile device application data category 7740, which includes data exchanged between and / or stored on a user's device, such as mobile device 7530. A further embodiment includes a garment controller data category 7770 that includes data exchanged and / or stored on it between garment controllers such as the controller 7520. In some embodiments, any of the data categories can include read / write access settings that limit access or provide a level of access. In some embodiments, the read / write access protocol and data transfer method can be configured to be HIPAA compliant.

In some embodiments, the healthcare provider can log in to the system's physician portal (website or software application, mobile app, etc.). In some embodiments, the website may allow the provider to register for an account. In some embodiments, the website may allow the provider to add a device (patient) to the patient list via a unique device ID. In some embodiments of the invention, the website can interact with a cloud server to display physician patient data. In some embodiments, the portal dashboard may allow a healthcare provider to browse the provider's patients or groups (healthcare-related) of patients. In some embodiments, the system can allow healthcare providers to customize the criteria for classifying patients (eg, using red / yellow / green / exclusion classification types). .. In some embodiments, the system utilizes push alerts (email, SMS, secure messages, etc.) via customizable criteria sent to the healthcare provider to zone the patient's desired progression. You can be notified if you are outside or at risk of readmission. For example, FIG. 78 shows a portion of the Provider Portal Dashboard 7800 that includes patient classification based on physician's customizable criteria so that physicians can receive alerts based on their preferences. For example, a patient compliance overview can include exemplary embodiments such as a green "OK" compliance alert. In another embodiment, the "warning" alert can be colored yellow. In another embodiment, the "criteria" alert can be colored red and the "exclusion" alert can be colored black or gray. One of ordinary skill in the art can understand that other colors, images, graphics, animations, or combinations thereof can be used to represent a compliance overview.

FIG. 79 shows a customizable panel and alert window 7900 of the provider portal dashboard according to some embodiments of the present invention. In some embodiments, the window 7900 is a monitoring (time) window (preoperative, postoperative, etc.) and / or utilization / compliance rate, and / or ROM, and / or extension, without limitation. A customization panel for classification & alerts can be provided, including and / or pain values.

Referring to FIG. 80, some embodiments include a provider portal patient list window 8000 that can be used to provide the patient list with visible flags indicating patient classification based on the provider's customized criteria. In some embodiments, the provider portal patient list window 8000 can include the ability to search / filter / sort records and / or add devices / patients to the patient list. In some embodiments, Window 8000 can be customized to provide a "My Patients" view and / or a "Group Patients" view.

Some embodiments include a graphic view of the patient's time series data having graphic and / or tabular data for the ROM. For example, FIG. 81 shows a patient overview window 8100 according to some embodiments of the present invention. (For example, flex / ext / ROM degree and / or NMES / TENS stimulation (power level, # session), and / or pain level (eg, vas scale), and / or activity level (eg, step), and / Alternatively, patient-reported outcome measurements (PROM) such as KOOS / KOOS JR / HOOS JR and / or rehabilitation goals are included.) In addition, FIG. Shows a format view. In some embodiments, windows 8100, 8200 can include a graphic / tabular toggle that can switch or cycle between a graphical data view and a tabular data view. In some embodiments, the system can allow the generation of a printable patient summary chart. For example, FIGS. 83A-83B and 84A-84B show printable patient summary charts according to some embodiments of the present invention. Some embodiments include formatted charts for printing or exporting, storing in PDF, storing in electronic medical records (EHR / EMR), etc.

In some embodiments, the system can display graphical and tabular data at the same time. For example, FIG. 85 shows a patient stimulation detail window 8500 according to some embodiments of the present invention. In some embodiments, the window 8500 can include a detailed graphic and tabular view of the time series stimulus data. In some embodiments, window 8500 displays the power level by zone and / or the number of completed sessions, and / or the stimulation time, and / or the number of sessions per week, and / or the details of the final session, and / Or can include any yellow / green flags based on customized settings. FIG. 86 shows a detailed window 8600 of the patient range of motion (ROM) according to some embodiments of the present invention. Some embodiments include a detailed graphic view and tabular view of time series ROM data, including, but not limited to, flexion (degrees), extension / hyperextension (degrees), and / or ROM (degrees). .. Other embodiments may include the number of sessions and / or final measurement details. Further embodiments can include coloring flags (eg, red / yellow / green flags, etc.) based on customizable settings.

Some embodiments are red / yellow / based on mean pain values (tube-visual analog scale) and / or pre / post stimulus session data and / or final measurement details and / or customizable settings. Includes a detailed graphical and tabular view of time series pain data including a green flag. For example, FIGS. 87-88 show patient pain detail windows 8700, 8800 according to some embodiments of the present invention. In addition, some embodiments may include a detailed graphical and tabular view of time series activity data, including mean day steps and / or final measurement details.

Some embodiments include passive range of motion data. For example, FIG. 89 shows a patient passive range of motion (PROM) 8900 according to some embodiments of the present invention. Some embodiments include, but are not limited to, a detailed graphical and tabular view of time series PROms data, including KOOS / KOOS JR, HOOS / HOOS JR, VR-12, patient satisfaction survey results. Some embodiments include classification and composite scores, data found by survey time points, and / or final measurement details.

Some embodiments include a real-time rehabilitation and tracking system. For example, in some embodiments, the patient can download a mobile application to pair the rehabilitation system with one or more personal mobile devices. For example, either the brace system or the assembly capable of capturing the above-mentioned range of motion (hereinafter, "ROM") can be a rehabilitation system that can be paired with a mobile device. In some embodiments, the mobile device application can serve as a user interface for activating the device via Bluetooth®. In some embodiments, the rehabilitation system performs NMES / TENS stimulation and / or ROM measurements and / or records pain levels and / or records activity levels and / or patients per desired time point. The reporting result scale (PROM) can be managed. In some embodiments, the mobile device can transmit all data depending on the system cloud server or cellular data (utilization data, measurements, patient profile information, etc.) via WiFi.

Various display screens produced by the real-time rehabilitation and tracking system are shown in FIGS. 90A-98. For example, FIG. 90A shows a start screen 9000 for a mobile application according to some embodiments of the present invention. In some embodiments, the screen 9000 can include a visual static or dynamic display of the representation in which the user is activating one or more components or assemblies of a real-time rehabilitation and tracking system. For example, in some embodiments, the patient can be illustrated as an access and activation of a brace system or assembly and any barcode or standard information.

In addition, FIG. 90B shows a scan screen of a mobile application according to some embodiments of the present invention. In some embodiments, the screen 9050 can include an explanatory diagram that scans the garment with a real-time rehabilitation and tracking system. In some embodiments, following a successful device scan, the device can display an information screen. For example, FIG. 90C shows an information screen of a mobile application according to some embodiments of the present invention. FIG. 91A shows a start stimulus screen 9100 for a mobile application according to some embodiments of the present invention. In some embodiments, the screen 9100 can include information related to treatment type and recommendations.

FIG. 91B shows a dashboard screen 9150 of a mobile application according to some embodiments of the present invention. In some embodiments, the screen 9150 may include home, stimulator, ROM and menu access icons. In some embodiments, the screen 9150 can include a daily progress indicator indicating a progressive session. In some embodiments, access tabs configured to access stimulation history and / or ROM / flexion-extension and / or pain, and / or steps can be provided. In some embodiments, the user can use the screen 9150 to reversibly access one or more of the access tabs using the screen 9150 as the main or control screen.

FIG. 92A shows a mobile application stimulator session start screen 9200 according to some embodiments of the present invention. In some embodiments, the screen 9200 can include instructions for the number of sessions of type and / or instructions for the part of the body to be treated, and / or treatment time, and / or recommended number of treatments and / Or can provide information about treatment, such as days or dates.

FIG. 92B shows a pain survey screen 9225 for a mobile application according to some embodiments of the present invention. In some embodiments, the screen 9225 can include a stimulation survey and can display a selectable gauge of pain levels. In some embodiments, the screen 9225 can be shown prior to the start of the stimulation session. In some embodiments, the system can display treatment program options prior to the start of treatment. For example, FIG. 92C shows a stimulus treatment screen 9250 for a mobile application according to some embodiments of the present invention. In some embodiments, the screen 9250 can display selection options for the "postoperative" and / or "intensity" program.

Some embodiments may include a stimulus alert window. FIG. 93A shows the stimulation level information screen 9300 of the mobile application according to some embodiments of the present invention. In some embodiments, a prompt may be displayed to prompt the user to start treatment when the user is ready to start treatment. 93B-93C, and 94A show stimulation level screens 9325, 9350, 9400 for mobile applications according to some embodiments of the present invention. In some embodiments, the screens 9325, 9350, 9400 may include an indication or display of the number of sessions of type and / or at least one stimulus level selector or indicator. In some embodiments, the stimulation level selector or indicator can include a toggle that increases or decreases the stimulation level, and an indicator indicating the stimulation level and / or a numerical indicator of the stimulation level. As shown in FIG. 94A, some embodiments include a timer display of the treatment session. In some embodiments, the stimulus can be stopped or paused. For example, FIG. 94B shows a mobile application stimulus information screen 9450 shown after a pause in a treatment session.

Some embodiments include display screens exemplifying ROM treatment. For example, FIG. 95A shows a range of motion (ROM) start screen 9500 for a mobile application according to some embodiments of the present invention. In some embodiments, the screen 9500 can include a stationary or moving image display of the ROM movement and an access or start icon that allows the user to start the ROM test. FIG. 95B shows a mobile application range of motion (ROM) connection screen 9525 according to some embodiments of the present invention. In some embodiments, the screen 9525 can include a display showing a ROM image or animation that allows the user to visualize the ROM. In some embodiments, the screen 9525 can include a flexion and / or extension and a ROM display. 95C and 96A show the range of motion (ROM) measurement screens 9550, 9600 of a mobile application according to some embodiments of the present invention. In some embodiments, the screens 9550, 9600 can include a ROM image or animation that allows the user to visualize the TOM measurement. FIG. 96B shows the range of motion (ROM) result screen 9625 of a mobile application according to some embodiments of the present invention. In some embodiments, the screen 9625 can include a ROM display based on one or more ROM treatment sessions. In some embodiments, the screen 9625 can include a ROM display of the target ROM and can include a target flexion and / or extension angle.

FIG. 97A shows a mobile application setting screen 9700 according to some embodiments of the present invention. In some embodiments, the screen 9700 may include a configuration display that includes one or more selectable or adjustable settings. For example, some embodiments include a selectable toggle for "stimulation complete". Some other embodiments include selectable toggles for "range of motion complete". Some other embodiments include selectable toggles for "electrode replacement". Some other embodiments include a selectable toggle for "My Profile Complete". Some other embodiments include range of motion adjustment. In some embodiments, either the selectable or adjustable setting can be selected to display one or more selectable icons or data fields. For example, FIG. 97B shows a profile screen 9725 of a mobile application according to some embodiments of the present invention. In some embodiments, the screen 9725 may include one or more selectable icons and / or data fields associated with the user's profile.

Shows his own set target screen 9750 of a mobile application according to some embodiments of the present invention. In some embodiments, the screen 9750 may include information related to one or more goals, and / or one or more selectable icons, and / or data fields related to the user's goals. .. FIG. 98 shows a stimulus help screen 9825 for a mobile application according to some embodiments of the present invention. In some embodiments, the screen 9825 can include one or more help topics related to stimulation or other treatment-related procedures or actions.

Although the present invention has been described above in the context of certain embodiments and examples, the invention is not necessarily so limited, and many other embodiments, examples, uses, modifications, and embodiments. It will be appreciated by those skilled in the art that deviations from form, example, and usage are intended to be covered by the appended claims. The entire disclosure of each patent and publication cited herein is incorporated by reference as if each such patent or publication was individually incorporated herein by reference. The various features and advantages of the present invention are described in the appended claims.

Claims (20)

A system with a plurality of electrodes including at least one active electrode and at least one passive electrode.
Each electrode is configured and arranged to physically contact the patient's skin to form an electrical circuit with the control electronics of at least one controller.
The electrical circuit is configured and arranged to measure electrical parameters using the at least one active electrode and the at least one passive electrode to form a closed-loop electrical muscle stimulation system.
The stimulus current or voltage applied to the skin between the at least one active electrode and the at least one passive electrode was measured through at least one program and the at least one active electrode and the at least one passive electrode. Based on at least one of the electrical parameters
The at least one controller
(A) A detected electrical pulse is applied to the tissue using at least one of the plurality of electrodes.
(B) The at least one electrical parameter from the tissue is measured and
(C) Using at least one of the active electrodes, a stimulus pulse is tunably applied to the tissue based at least in part based on the measured electrical parameters, and the stimulus pulse is the at least one. Adjustably controlled by a controller to maintain a constant power output to the tissue based at least in part on the at least one electrical parameter.
(D) Repeat steps (a) to (c),
Configured and arranged as
The system further comprises an article coupled to at least one computer-readable medium configured to store usage data, wherein the usage data is related to the patient's use of the article. The system of claim 1, further comprising a computer program, applet or application configured to upload said usage data for analysis. The system of claim 2, wherein the at least one controller is configured and arranged to electromagnetically couple with a mobile computing device using at least a portion of the computer program, applet or application. At least a portion of the computer program, applet or application is configured and arranged to include at least one user interface on the user's computing device, the at least one user interface displaying at least some usage data. The system of claim 3, wherein the system is configured to allow control of the parameters of the article. The at least one controller is configured to update the at least one user interface with at least one of the state of a portion of the article, the position of the portion of the article, and data from at least one sensor in the system. The system according to claim 4. The system of claim 4, wherein the at least one user interface comprises a display that includes an option to scan the article and synchronize it with the at least one controller. The system of claim 4, wherein the at least one user interface comprises a display that includes an option to scan and synchronize more than one of the articles. The system of claim 4, wherein the at least one user interface comprises a display that includes an option to activate a wired or wireless link that connects the article to the at least one controller. The system of claim 6, wherein the display is configured and arranged to allow the user to set or reconfigure at least one stimulus pulse. The display is one or 2 associated with at least one of the stimuli provided by at least a portion of the article and the range of motion measured by at least a portion of the article by at least a portion of the computer program, applet or application. The system according to claim 6, which can be configured to display the above parameters. The display relates to a stimulus provided by at least a portion of the article and a range of motion measured by at least a portion of the article by at least a portion of the computer program, applet or application. The system of claim 6, which can be configured to provide a visual representation of the behavior of the user wearing at least a portion. The computing device comprises at least one of a desktop computer, a laptop computer, a digital tablet, a digital information terminal, a mobile phone or smartphone, a smartwatch, a wearable activity monitor, glasses, a camera, a pager, and an internet appliance. The system according to claim 4. The system of claim 1, wherein the article comprises a brace assembly. 13. The system of claim 13, wherein the brace assembly comprises at least one of a brace, stay, sleeve, band, sling, garment, wrap, and strap. The at least one sensor is an accelerometer, a motion sensor, a proximity sensor, an optical sensor, a motion sensor, a gyrometer, a magnetometer, a proximity sensor, a hydration sensor, a force or pressure sensor, a position sensor, a global positioning sensor (GPS). , Optical sensor, magnetic sensor, magnetometer, induction sensor, capacitance sensor, eddy current sensor, resistance sensor, magnetic resistance sensor, induction sensor, infrared sensor, tilt meter sensor, piezoelectric material or piezoelectric base sensor, blood oxygen The system of claim 5, comprising at least one of a sensor, a heart rate sensor, a laser or ultrasonic based sensor, and an electromyogram type sensor. A remote server containing a computer program, applet or application configured to initiate or maintain the exchange of usage data between the article and the server and / or between the combined mobile computing device and the server. The system according to claim 1, further comprising. The server is configured as a host to a web portal or is coupled to a host server that provides the web portal, which is to the usage data or at least one parameter associated with the use of at least a portion of the article. 16. The system of claim 16, configured to access or display. The web portal is configured to generate one or more alerts based on at least one user customization criteria related to the usage data, the criteria being the usage level of at least a portion of the article by the user, by the user. At least of the usage limits of at least a portion of the article, the usage time of at least a portion of the article by the user, the usage type of at least a portion of the article by the user, and the behavior of at least a portion of the article in use by the user. 17. The system of claim 17, which may include one. 18. The system of claim 18, wherein the alert comprises at least one of an email, text or SMS message, display icon, rendered text, rendered graphic, categorized or customized alert. The at least one user customization criterion is at least one of a monitoring window, utilization and / or activity level, one or more designated compliance or rehabilitation goals, compliance rate, range of motion (ROM), and pain value. The system of claim 18, including.

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