WO2017183994A1 - Measurement device for detecting and measuring pain - Google Patents
Measurement device for detecting and measuring pain Download PDFInfo
- Publication number
- WO2017183994A1 WO2017183994A1 PCT/NO2017/050098 NO2017050098W WO2017183994A1 WO 2017183994 A1 WO2017183994 A1 WO 2017183994A1 NO 2017050098 W NO2017050098 W NO 2017050098W WO 2017183994 A1 WO2017183994 A1 WO 2017183994A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- measurement device
- force sensor
- flexible membrane
- closed volume
- force
- Prior art date
Links
- 238000005259 measurement Methods 0.000 title claims abstract description 111
- 208000002193 Pain Diseases 0.000 title claims abstract description 40
- 230000036407 pain Effects 0.000 title claims abstract description 39
- 239000012528 membrane Substances 0.000 claims abstract description 52
- 230000009429 distress Effects 0.000 claims abstract description 6
- 230000004913 activation Effects 0.000 claims description 21
- 238000004891 communication Methods 0.000 claims description 17
- 239000012530 fluid Substances 0.000 claims description 10
- 230000003213 activating effect Effects 0.000 claims description 9
- 230000001419 dependent effect Effects 0.000 claims description 4
- 239000013013 elastic material Substances 0.000 claims description 4
- 238000003825 pressing Methods 0.000 claims description 2
- 239000007788 liquid Substances 0.000 description 8
- 230000003321 amplification Effects 0.000 description 3
- 230000009849 deactivation Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000003199 nucleic acid amplification method Methods 0.000 description 3
- 239000011148 porous material Substances 0.000 description 3
- WBHQEUPUMONIKF-UHFFFAOYSA-N PCB180 Chemical compound C1=C(Cl)C(Cl)=CC(Cl)=C1C1=CC(Cl)=C(Cl)C(Cl)=C1Cl WBHQEUPUMONIKF-UHFFFAOYSA-N 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000001953 sensory effect Effects 0.000 description 2
- 208000000094 Chronic Pain Diseases 0.000 description 1
- 208000000114 Pain Threshold Diseases 0.000 description 1
- 208000007271 Substance Withdrawal Syndrome Diseases 0.000 description 1
- 238000004026 adhesive bonding Methods 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000001149 cognitive effect Effects 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 238000003745 diagnosis Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008451 emotion Effects 0.000 description 1
- 230000002996 emotional effect Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000000968 intestinal effect Effects 0.000 description 1
- 229940124583 pain medication Drugs 0.000 description 1
- 230000037040 pain threshold Effects 0.000 description 1
- 230000037325 pain tolerance Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01L—MEASURING FORCE, STRESS, TORQUE, WORK, MECHANICAL POWER, MECHANICAL EFFICIENCY, OR FLUID PRESSURE
- G01L1/00—Measuring force or stress, in general
- G01L1/20—Measuring force or stress, in general by measuring variations in ohmic resistance of solid materials or of electrically-conductive fluids; by making use of electrokinetic cells, i.e. liquid-containing cells wherein an electrical potential is produced or varied upon the application of stress
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/48—Other medical applications
- A61B5/4824—Touch or pain perception evaluation
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/0002—Remote monitoring of patients using telemetry, e.g. transmission of vital signals via a communication network
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/103—Detecting, measuring or recording devices for testing the shape, pattern, colour, size or movement of the body or parts thereof, for diagnostic purposes
- A61B5/11—Measuring movement of the entire body or parts thereof, e.g. head or hand tremor, mobility of a limb
- A61B5/1124—Determining motor skills
- A61B5/1125—Grasping motions of hands
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/16—Devices for psychotechnics; Testing reaction times ; Devices for evaluating the psychological state
- A61B5/165—Evaluating the state of mind, e.g. depression, anxiety
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/22—Ergometry; Measuring muscular strength or the force of a muscular blow
- A61B5/224—Measuring muscular strength
- A61B5/225—Measuring muscular strength of the fingers, e.g. by monitoring hand-grip force
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
- A61B5/6801—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be attached to or worn on the body surface
- A61B5/6813—Specially adapted to be attached to a specific body part
- A61B5/6825—Hand
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B2562/00—Details of sensors; Constructional details of sensor housings or probes; Accessories for sensors
- A61B2562/02—Details of sensors specially adapted for in-vivo measurements
- A61B2562/0247—Pressure sensors
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/22—Ergometry; Measuring muscular strength or the force of a muscular blow
Definitions
- the invention relates to a measurement device for detecting and measuring pain, distress or other discomfort of a user.
- the invention also relates to a readout activation system for activating reading out of such measurement device.
- VAS Visual Analog Scale
- the patient marks the point on the line corresponding to his pain.
- the NRS Numerical Rating Scale
- the VAS is used the most since it is not at all complicated and does not require any great explanations.
- the problem with such scales is, however, that as a person completing the scale one generally tends toward the centre and is averse to marking the extremes.
- users also tend toward an evaluation, which becomes closer and closer (convergence) with different pain intensity.
- the most important pain questionnaire is the McGill Pain Questionnaire (MPQ).
- MPQ McGill Pain Questionnaire
- the patient is given a large choice of adjectives of which he checks the ones, which correspond to his pain.
- the adjectives are divided into three classes: sensory, affective and evaluative. A plurality of aspects of the pain are thus admittedly detected, but filling out takes a long time and the patient also has to understand and/or know all the adjectives to be able to complete the MPQ correctly.
- WO2009/052100A1 discloses a further apparatus for measuring pain.
- This apparatus has the disadvantage that the pain can only be measured with extreme imprecision and that the apparatus is only suitable to measure intestinal pain.
- US2013/0046205A1 discloses a device for detecting and measuring pain felt by a person.
- Said device comprises a pressure or force sensor, a hollow body having an outer sleeve and an inner space, and an electronic unit for detecting the signal of the pressure or force sensor.
- the outer sleeve of the hollow body is embodied in such a way that it can be at least partially surrounded by a hand, the inner space of the hollow body is filled with a non-gaseous elastic material or a non-gaseous fluid, and the pressure or force sensor is arranged in such a way that the pressure of the elastic material or the fluid can be measured.
- the device may be read out by a computer in the physician's office. The logged date may then be read out, presented in a graph, and assessed by the physician, who now gets a much clearer and accurate picture of the pain history of the patient.
- the invention has for its object to remedy or to reduce at least one of the drawbacks of the prior art, or at least provide a useful alternative to prior art.
- the invention in a first aspect, relates to a measurement device for detecting and measuring pain or other discomfort of a user.
- the measurement device comprises: i) an external housing having at least partially flexible walls and being configured for being held and squeezed by a hand of the user, wherein the external housing defines a first closed volume, and ii) a force sensor for detecting and measuring pressure in the first closed volume.
- the measurement device further comprises an inner housing, wherein the inner housing defines a second closed volume, the second closed volume comprising the force sensor, wherein the inner housing comprises a flexible membrane that is placed such that the flexible membrane faces the first closed volume at a first side of the flexible membrane and faces the force sensor at a second, opposite, side of the flexible membrane, wherein the flexible membrane is positioned such that there is a gap between the flexible membrane and the force sensor when no force is applied by the user to the external housing. Furthermore, at a certain predefined pressure applied by the user the flexible membrane touches the force sensor, wherein the force sensor from that instant starts to register a force.
- an internal housing comprising the force sensor.
- the second housing defines a second closed volume within the first closed volume.
- the housing further comprises a flexible membrane, which on one side faces the first closed volume, and on the other side the force sensor.
- the internal housing is designed such that a gap is provided between said membrane and the force sensor, when the measurement device is at rest.
- closed volume is a space within a housing that is closed, wherein said space may be filed with a fluid (gas or liquid), but also flexible material.
- the housing obviously does not need to be fluid tight (so the word “closed” does not necessarily mean air or liquid tight), but when a liquid or gas is used it should preferably be (liquid/air) tight (or sealed).
- volume other words could be used as well, such as "space”, “chamber”, “room”, “enclosure”, "region”, or the like. It is submitted that all these different words have a commonality, namely that it may contain or comprise things like other components, gas, liquid, flexible material, porous material, or combinations of the above, etc.
- the flexible membrane is provided with a protruding element at the second side, wherein the protruding element is configured for pressing on the force sensor when the flexible membrane is pushed towards the force sensor upon the application of the force on the external housing by the hand of the user.
- This embodiment conveniently increases the sensitivity of the measurement device, starting from the threshold force, because as soon as the protruding element touches the force sensor the force (pressure) applied to the force sensor is higher than what it would have been without the protruding element.
- this embodiment is particularly advantageous when the flexible area is larger than the area of the force sensor.
- the protruding element is designed to have a contact area when pushed to be in contact with the force sensor, wherein the contact area is designed to be a predefined factor smaller than a membrane area of the flexible membrane.
- the amplification factor of the force applied by the membrane is roughly determined by the area of the flexible membrane divided by the contact area of the protruding element.
- the measurement device further comprises an electronic circuit coupled with the force sensor for controlling and reading out the force sensor and for storing the measurements.
- the electronic circuit may register when the measurement device is squeezed, how long this took place, and how much force was applied (which is an indication of the level of pain, discomfort or distress).
- the measurement device further comprises a battery for supplying power to the electronic circuit.
- a battery-powered device when the measurement device is to be carried by a user all day long, and when it has to be used at all places he or she may be.
- Such battery-powered device when being small, portable, and handheld, is also inconspicuous, which offers the user privacy, i.e. nobody will know he or she carries such device.
- the electronic circuit further comprises a communication circuit for communicating registered data with a readout system.
- a communication circuit for communicating registered data with a readout system.
- such communication circuit comprises a wireless communication circuit, such as a Bluetooth transceiver circuit.
- the electronic circuit further comprises a switching circuit, which is configured for deactivating part of the electronic circuit, preferably at least the communication circuit, during the time that the measurement device is not being read out by a readout system, and for activating the part during the time that the measurement device is to be read out by the readout system.
- Battery lifetime is of high importance. This problem is also acknowledged in Kanjo, E., Al- Husain, L, & Chamberlain, A. (2015). Emotions in context: examining pervasive affective sensing systems, applications, and analyses. PersUbiq Compute 19(7), (1 197-1212). As pointed out in Kanjo et.
- the switching circuit is controllable by a magnetic field
- This embodiment conveniently cooperates with a so-called readout activation system that the inventors developed together with the measurement device.
- This readout activation system may be conveniently provided with one or more magnets such that the presence of a magnetic field may trigger the measurement device to activate said part of the circuitry, including the communication circuit. Similarly, the absence of the magnetic field will trigger the measurement device to deactivate said part of the circuitry.
- the inner housing further comprises a space for containing respective components other than the force sensor.
- the electric circuit may be conveniently placed within this space, for example in the form of a printed-circuit board (PCB).
- PCB printed-circuit board
- the inner housing is suspended within the first closed volume of the external housing by means of a positioning member that fixes the inner housing to the inside of the external housing.
- the inner housing is preferably suspended in the middle of the first closed volume such that during squeezing the user does not experience any obstructions.
- the force sensor comprises a force-sensitive resistor.
- the force-sensitive resistor provides for a low-power solution, because it only provides for a measurement signal when a force is applied to it. Thus in rest, no power is consumed, which increases the battery lifetime significantly.
- the first closed volume is at least partially filled with a fluid or an elastic material.
- the fluid may be a liquid or a gas.
- the first closed volume could contain an elastic porous material, which regains its form after squeezing it, wherein the pores are filled with a fluid.
- the second closed volume is at least partially filled with a further fluid for converting a pressure on the flexible membrane into a pressure applied to the force sensor.
- a further fluid for converting a pressure on the flexible membrane into a pressure applied to the force sensor.
- special measures may be necessary for protection of the force sensor. Either the force sensor has to be able to tolerate contact with liquid or it has to be properly sealed.
- the invention relates to a readout activation system for activating reading out of the measurement device in accordance with claim 14.
- the readout activation system for activating the measurement device belongs to a group of embodiments of the measurement device of the invention, in particular those that comprise a switch for deactivating part of the electronic circuit.
- the readout activation system comprises a receiving region, such as a recess, for receiving the measurement device, and further comprises at least one magnet configured for generating a magnetic field for controlling the switching circuit for activating or deactivating the part of the electronic circuit when the measurement device is put in or taken from the receiving region, respectively.
- This embodiment of the readout activation system conveniently cooperates with the embodiments of the measurement device of the invention, which comprise the switch that is activated by a magnetic field.
- Fig. 1 shows an exploded view of an embodiment of the measurement device in accordance with the invention
- Fig. 2 shows an enlarged cross-sectional view of part of the measurement device of
- Figs. 3a-3c illustrate some aspects of the functioning of the measurement device of the invention
- Figs. 4a-4d illustrate some other aspects of the functioning of the measurement device of the invention
- Figs. 5a-5c illustrate an embodiment of a readout activation system and a readout system for reading out said measurement device in accordance with the invention
- Figs. 5a-5c illustrate an embodiment of a readout activation system and a readout system for reading out said measurement device in accordance with the invention
- the present invention relates to a measurement device for detecting and measuring pain, distress, or other discomfort of a user.
- the core of this measurement device is a pressure registration unit for registration of the pressure, which a user applies to the unit.
- the pressure registration unit will preferably be arranged to be able to register pressure in combination with time, such that it may be registered, for instance, when the user applies pressure to the unit, for how long the user applies the pressure, and how much pressure is applied.
- the pressure registration unit according to the invention can be used for instance in the fields of medicine, psychiatry, child welfare, and similar fields.
- the invention can be of a size which fits into the hand of the user.
- the purpose of the invention is to help the user and their therapist (or similar) to register for instance chronic pain, fear, withdrawal symptoms, and so on. Reference is made to US2013/0046205 for more background information and explanation on using such device and why it is beneficial.
- Fig. 1 shows an exploded view of an embodiment of the measurement device 100 in accordance with the invention.
- the measurement device 100 comprises an external housing 110 having flexible walls 110w.
- the external housing 110 defines (alternatively the words "encloses or isolates" could be used in this context) a first closed volume 105.
- the housing 110 comprises two parts 10a, 110b that are mounted together (through gluing, screwing, clamping, or the like).
- the measurement device 100 further comprises an internal housing 150, which is suspended within the external housing 110 by means of a positioning member 125 as shown.
- the positioning member 125 is preferably also flexible.
- the internal housing 150 comprises a first part 151 , which may be non- flexible or at least much less flexible than the external housing 110.
- the first part 151 of the internal housing partially defines a first space 155, which comprises a force sensor 170, which preferably is a force-sensitive resistor (FSR), because of its low power consumption advantage.
- the first space 155 is further sealed off by a flexible membrane 152, which in this embodiment is to be clicked over said first part 151 of the internal housing 150 and held in place with an O-ring 160, as illustrated.
- the membrane 152 in this embodiment is provided with a protruding element 152p, which is advantageous as discussed in the introduction of this specification.
- Fig. 2 shows an enlarged cross-sectional view of the part of the measurement device of Fig. 1.
- the flexible membrane 152 has been mounted on the first part 151 of the internal housing 150.
- the second closed volume 155 (earlier mentioned first space) is formed. It is illustrated how the flexible membrane 152 faces the first closed volume 105 on a first side 152s1 thereof, and the force sensor 170 on a second, opposite, side 152s2 thereof.
- the figure further illustrates that there is a gap 152d between said protruding part 152p and the force sensor 170.
- Another aspect that Fig. 2 illustrates is the amplification of the pressure/force applied to the membrane 152.
- the pressure in the first closed volume 105 presses on an area 152a with the size as illustrated by the arrow. Under this pressure the membrane 152 may bend towards the force sensor 170. As soon as the protruding element 152p of the membrane touches the force sensor 170 it is the contact area 152pa of the protruding element 152p, as illustrated by the other arrow, which will transfer the force to the force sensor 170. This force/pressure is effectively an amplified version of the force applied to the membrane 152.
- the amplification factor is typically in the order of the ratio between the membrane area 152a and the contact area 152pa of the protruding element 152.
- Fig. 2 further illustrates that the force sensor 170 is connected to a printed-circuit board (PCB) 180 via a connecting wire (or wires) 171.
- the PCB 180 is provided in a second space 181 of the internal housing 150 as illustrated.
- the PCB 180 is provided with en electronic circuit 182 (i.e. an integrated circuit), which may comprise a processor or control unit for controlling and reading out the force sensor 170 and storage circuitry for storing said measurements).
- the electronic circuit 182 in this embodiment also comprises a switching circuit 184 and a communication circuit 186.
- the communication circuit 186 may be a Bluetooth transceiver circuit, which as such is well-known to the person skilled in the art.
- the electronic circuit is power by a battery 190.
- the switching circuit 184 has been added to facilitate deactivating part of the electronic circuit 182, in particular the communication circuit 186, for reasons as earlier discussed, i.e. save power and thereby increase battery lifetime.
- Figs. 3a-3c illustrate some aspects of the functioning of the measurement device of the invention.
- the hand 200 of the user applies the so-called threshold pressure to the measurement device 100.
- the flexible membrane 152, or the protruding element 152p if present barely touches the force sensor 170, i.e. it begins to apply a small force when the force applied to the measurement device 100 is further increased.
- Fig. 3b shows the situation where the user applies a medium force to the measurement device. In this situation the flexible membrane 152, or the protruding element 152p if present, applies a force to the force sensor 170.
- Fig. 3c shows the situation where the user applies a maximum force to the measurement device. With “maximum force” it is meant the maximum force that can be registered, not the maximum force that could be applied.
- the force sensor 170 in this situation outputs its maximum signal level to the electronic circuit 180.
- Figs. 4a-4d illustrate some other aspects of the functioning of the measurement device of the invention.
- Fig. 4a shows the equilibrium situation, where the user does not apply a pressure to the measurement device 100. Consequently, the membrane 152 applies a zero force F0 to the force sensor 170 (although there is still the pressure in the 155 second closed volume, which applies a pressure on the force sensor 170).
- Fig. 4b shows the situation which complies with Fig. 3a.
- a minimum force Fmn is applied to the force sensor 170.
- Fig. 4c shows the situation that complies with Fig. 3b.
- a medium force Fmd is applied to the force sensor 170.
- Fig. 4d shows the situation that complies with Fig. 3c.
- the maximum registerable force Fmx is applied to the force sensor 170.
- the reason for differentiating between F0 and Fmn is that the force sensor may be very sensitive (for instance when an FSR is used).
- the force sensor may be very sensitive (for instance when an FSR is used).
- the pressure is registered by the measurement device 100.
- the small-signal behaviour in these two situations is very different.
- Figs. 5a-5c illustrate an embodiment of a readout activation system 300 and a readout system for reading out said measurement device in accordance with the invention.
- the communication circuit 182 only needs to be active when the measurement device 100 is read out by a readout system (i.e. laptop, table, PC, smartphone) 400.
- the measurement device 100 may comprise a switching circuit for (triggering) deactivating said communication 182 (and/or other parts).
- the deactivation is done in software.
- the measurement device 100 is configured such, that when it is put in the readout activation device 300 (also called the crib) it will broadcast and be ready for connection for a predefined time, for instance 30 seconds. After this time has lapsed, the measurement device 100 will return to its sleep mode again (arranged in software) even if the measurement device 100 remains in the crib 300.
- the readout activation system 300 which comprises in this embodiment a receiving region 310 (such as a recess) for receiving the measurement device 100 in accordance with the invention.
- a receiving region 310 such as a recess
- the readout activation system 300 is preferably put within Bluetooth communication reach of the readout system 400.
- the measurement device 100 is put into the recess 310.
- the measurement device 100 is activated by the readout activation system 300 and transmits its registered data to the readout system 400 via a wireless communication signal 999 as schematically illustrated.
- the registered data may be shown on the readout system 400 in the form of a graph 410 for example.
- the physician may subsequently interpret the registered data, which forms an indication of the pain, distress or other discomfort of the user over a certain period.
- Fig. 6 illustrates the operation of the readout activation system 300.
- This figure is very schematic in order to facilitate understanding of the principle.
- a plurality (but at least one) of magnets 350 as illustrated. These could be permanent magnets, but also other magnets are possible.
- These magnets 350 generate a magnetic field 355, which subsequently trigger the earlier-discussed switching circuit 184 to activate the communication circuit (not shown in Fig. 6), for instance by closing or opening when the measurement device 100 is placed in the recess 310.
- the switching circuit 184 be used to directly switch (on or off) the respective part electronically (i.e. in hardware), but it could also be used to trigger the deactivation through software.
- the measurement device in accordance with the invention is possible without deviating from the scope of protection as defined by the claims. It must be stressed that the protruding element of the membrane is optional, yet results in an advantage when used. In addition, the measurement device may have other forms than illustrated. Furthermore, the second closed volume may be provided outside the first closed volume if so desired, wherein the flexible membrane then effectively forms the interface between both volumes.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Biophysics (AREA)
- Pathology (AREA)
- Public Health (AREA)
- Biomedical Technology (AREA)
- Heart & Thoracic Surgery (AREA)
- Medical Informatics (AREA)
- Molecular Biology (AREA)
- Surgery (AREA)
- General Health & Medical Sciences (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Social Psychology (AREA)
- Pain & Pain Management (AREA)
- Child & Adolescent Psychology (AREA)
- Developmental Disabilities (AREA)
- Educational Technology (AREA)
- Psychology (AREA)
- Physiology (AREA)
- General Physics & Mathematics (AREA)
- Dentistry (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Computer Networks & Wireless Communication (AREA)
- Physical Education & Sports Medicine (AREA)
- Measuring And Recording Apparatus For Diagnosis (AREA)
- Measuring Pulse, Heart Rate, Blood Pressure Or Blood Flow (AREA)
Abstract
The invention relates to a measurement device (100) for detecting and measuring pain, distress, or other discomfort of a user. The measurement device (100) comprises: i) an external housing (110) having at least partially flexible walls (110w) and being configured for being held and squeezed by a hand (200) of the user, wherein the external housing (110) defines a first closed volume (105), and a force sensor (170) for detecting and measuring pressure in the first closed volume (105). The measurement device (100) further comprises an inner housing (150) located within the external housing (110), wherein the inner housing (150) defines a second closed volume (155), the second closed volume (155) comprising the force sensor (170), wherein the inner housing (150) comprises a flexible membrane (152) that is placed such that the flexible membrane (152) faces the first closed volume (105) at a first side (152s1) of the flexible membrane (152) and faces the force sensor (170) at a second, opposite, side (152s2) of the flexible membrane (152), wherein the flexible membrane (152) is positioned such that there is a gap (152d) between the flexible membrane (152) and the force sensor (170) when no force is applied by the user to the external housing (110). The measurement device in accordance with the invention may be more accurate, more robust, more endurable and more user-friendly.
Description
MEASUREMENT DEVICE FOR DETECTING AND MEASURING PAIN
FIELD OF THE INVENTION
The invention relates to a measurement device for detecting and measuring pain, distress or other discomfort of a user. The invention also relates to a readout activation system for activating reading out of such measurement device.
BACKGROUND OF THE INVENTION
Pain is one of the most frequent reasons for consulting a physician. The patient often cannot give a clearly understandable answer to the physician's question of how severe the pain is. Either the patient cannot find the right words or the physician does not understand the words used. This is inter alia because pain is a subjective sense impression, which includes sensory, cognitive and emotional aspects. An accurate measurement of pain is, however, very important, e.g. for diagnosis, when adjusting the medicinal pain therapy or in pain medication research. A plurality of methods of detecting pain have been developed to date. Most of them can be divided into two categories: One-dimensional pain scales and multidimensional pain questionnaires. The most important one-dimensional scale is the "Visual Analog Scale" (VAS). It consists of a 10cm long line whose left end is marked by "No pain" and whose right end is marked by ""Very severe pain". The patient marks the point on the line corresponding to his pain. The NRS (Numerical Rating Scale), where the selection of a number from 0-10 is communicated verbally to represent the pain, is closely related to the VAS. The VAS is used the most since it is not at all complicated and does not require any great explanations. The problem with such scales is, however, that as a person completing the scale one generally tends toward the centre and is averse to marking the extremes. On a multiple use of the VAS, users also tend toward an evaluation, which becomes closer and closer (convergence) with different pain intensity. This has the
consequence that the physician acquires the impression with the detection method that only small changes are present. The most important pain questionnaire is the McGill Pain Questionnaire (MPQ). The patient is given a large choice of adjectives of which he checks the ones, which correspond to his pain. The adjectives are divided into three classes: sensory, affective and evaluative. A plurality of aspects of the pain are thus admittedly detected, but filling out takes a long time and the patient also has to understand and/or know all the adjectives to be able to complete the MPQ correctly.
There are various technical devices to detect pain, for example the apparatus disclosed in EP0,874,587B1. They are, however, mostly computerized variants of the known scales VAS or questionnaires MPQ, including their disadvantages. There are furthermore devices for applying pain stimuli for the measurement of pain thresholds and pain tolerance, e.g. the apparatus disclosed in WO2004/103230A1.
WO2009/052100A1 discloses a further apparatus for measuring pain. This apparatus has the disadvantage that the pain can only be measured with extreme imprecision and that the apparatus is only suitable to measure intestinal pain.
US2013/0046205A1 discloses a device for detecting and measuring pain felt by a person. Said device comprises a pressure or force sensor, a hollow body having an outer sleeve and an inner space, and an electronic unit for detecting the signal of the pressure or force sensor. The outer sleeve of the hollow body is embodied in such a way that it can be at least partially surrounded by a hand, the inner space of the hollow body is filled with a non-gaseous elastic material or a non-gaseous fluid, and the pressure or force sensor is arranged in such a way that the pressure of the elastic material or the fluid can be measured. When the person (the patient) feels pain he or she intuitively squeezes the hollow body thereby applying a pressure to the force sensor, which is indicated for the amount of pain the person experienced. It has been shown by experiments that these measurements are quite effective and much more accurate than the earlier described methods of registering pain. Moreover, the device may be read out by a computer in the physician's office. The logged date may then be read out, presented in a graph, and assessed by the physician, who now gets a much clearer and accurate picture of the pain history of the patient.
Despite the latest developments in the prior art, there is still a need for further improving this technology to render the device more accurate, more robust, portable, more endurable, and more user-friendly.
SUMMARY OF THE INVENTION
The invention has for its object to remedy or to reduce at least one of the drawbacks of the prior art, or at least provide a useful alternative to prior art.
The object is achieved through features, which are specified in the description below and in the claims that follow.
The invention is defined by the independent patent claims. The dependent claims define advantageous embodiments of the invention.
In a first aspect, the invention relates to a measurement device for detecting and measuring pain or other discomfort of a user. The measurement device comprises: i) an external housing having at least partially flexible walls and being configured for being held and squeezed by a hand of the user, wherein the external housing defines a first closed volume, and ii) a force sensor for detecting and measuring pressure in the first closed volume. The measurement device further comprises an inner housing, wherein the inner housing defines a second closed volume, the second closed volume comprising the force sensor, wherein the inner housing comprises a flexible membrane that is placed such that the flexible membrane faces the first closed volume at a first side of the flexible membrane and faces the force sensor at a second, opposite, side of the flexible membrane, wherein the flexible membrane is positioned such that there is a gap between the flexible membrane and the force sensor when no force is applied by the user to the external housing. Furthermore, at a certain predefined pressure applied by the user the flexible membrane touches the force sensor, wherein the force sensor from that instant starts to register a force.
The effects of the measurement device in accordance with the invention may be understood as follows. In the invention an internal housing is provided, wherein the internal housing comprises the force sensor. The second housing defines a second closed volume within the first closed volume. The housing further comprises a flexible membrane, which on one side faces the first closed volume, and on the other side the force sensor. The internal housing is designed such that a gap is provided between said membrane and the force sensor, when the measurement device is at rest. The advantage of this measurement device with respect to the known measurement device as discussed earlier is that the design of the invention effectively builds in a certain threshold force above which the measurement device detects and measures a pressure in the first closed volume (i.e. when the measurement device is squeezed), and below which no force is detected and
measured. When a force is applied to the external housing, which increases the pressure in the first closed volume, this pressure first has to overcome a reaction force of the membrane, thereby pushing it closer to the force sensor. At a certain predefined pressure the membrane will touch the force sensor, which from that instant start to register a force. The inventor has realized that using a small threshold force will not severely deteriorate the reliability of the pain or discomfort measurement, i.e. a patient will always exceed such threshold force, in case of pain or discomfort. The inventor has also realized the user using the measurement device will typically carry it in a pocket or bag. While doing so the measurement device might be squeezed or deformed unintentionally, thereby creating the risk of unintentional registration of pain or discomfort. The invention thus conveniently reduces this risk by implementing the threshold force as described above.
A few terms used in this specification will be explained hereinafter.
Wherever the wording "closed volume" is used this is to be interpreted as a space within a housing that is closed, wherein said space may be filed with a fluid (gas or liquid), but also flexible material. When a flexible material is used, the housing obviously does not need to be fluid tight (so the word "closed" does not necessarily mean air or liquid tight), but when a liquid or gas is used it should preferably be (liquid/air) tight (or sealed). For the word "volume", other words could be used as well, such as "space", "chamber", "room", "enclosure", "region", or the like. It is submitted that all these different words have a commonality, namely that it may contain or comprise things like other components, gas, liquid, flexible material, porous material, or combinations of the above, etc.
In an embodiment of the measurement device in accordance with the invention the flexible membrane is provided with a protruding element at the second side, wherein the protruding element is configured for pressing on the force sensor when the flexible membrane is pushed towards the force sensor upon the application of the force on the external housing by the hand of the user. This embodiment conveniently increases the sensitivity of the measurement device, starting from the threshold force, because as soon as the protruding element touches the force sensor the force (pressure) applied to the force sensor is higher than what it would have been without the protruding element. Moreover, this embodiment is particularly advantageous when the flexible area is larger than the area of the force sensor.
In an embodiment of the measurement device in accordance with the invention the protruding element is designed to have a contact area when pushed to be in contact with the
force sensor, wherein the contact area is designed to be a predefined factor smaller than a membrane area of the flexible membrane. The amplification factor of the force applied by the membrane is roughly determined by the area of the flexible membrane divided by the contact area of the protruding element.
In an embodiment of the measurement device in accordance with the invention the measurement device further comprises an electronic circuit coupled with the force sensor for controlling and reading out the force sensor and for storing the measurements. The electronic circuit may register when the measurement device is squeezed, how long this took place, and how much force was applied (which is an indication of the level of pain, discomfort or distress).
In an embodiment of the measurement device in accordance with the invention the measurement device further comprises a battery for supplying power to the electronic circuit. It is convenient to use a battery-powered device, when the measurement device is to be carried by a user all day long, and when it has to be used at all places he or she may be. Such battery-powered device, when being small, portable, and handheld, is also inconspicuous, which offers the user privacy, i.e. nobody will know he or she carries such device.
In an embodiment of the measurement device in accordance with the invention the electronic circuit further comprises a communication circuit for communicating registered data with a readout system. Preferably, such communication circuit comprises a wireless communication circuit, such as a Bluetooth transceiver circuit.
In an embodiment of the measurement device in accordance with the invention the electronic circuit further comprises a switching circuit, which is configured for deactivating part of the electronic circuit, preferably at least the communication circuit, during the time that the measurement device is not being read out by a readout system, and for activating the part during the time that the measurement device is to be read out by the readout system. Battery lifetime is of high importance. This problem is also acknowledged in Kanjo, E., Al- Husain, L, & Chamberlain, A. (2015). Emotions in context: examining pervasive affective sensing systems, applications, and analyses. PersUbiq Compute 19(7), (1 197-1212). As pointed out in Kanjo et. a!., applications used in affective sensing pose a challenge to hardware designers, as the continuous availability of the application can be a drain on available power resources. The inventors have realized that certain circuitry, such as the communication circuit (Bluetooth) can easily be switched off during normal use (non-
readout) of the measurement device. The switching circuit does not necessarily need to directly switch the respective part electronically (i.e. in hardware), but could also be used to trigger the deactivation through software.
In an embodiment of the measurement device in accordance with the invention the switching circuit is controllable by a magnetic field, This embodiment conveniently cooperates with a so-called readout activation system that the inventors developed together with the measurement device. This readout activation system may be conveniently provided with one or more magnets such that the presence of a magnetic field may trigger the measurement device to activate said part of the circuitry, including the communication circuit. Similarly, the absence of the magnetic field will trigger the measurement device to deactivate said part of the circuitry.
In an embodiment of the measurement device in accordance with the invention the inner housing further comprises a space for containing respective components other than the force sensor. The electric circuit may be conveniently placed within this space, for example in the form of a printed-circuit board (PCB).
In an embodiment of the measurement device In accordance with the invention the inner housing is suspended within the first closed volume of the external housing by means of a positioning member that fixes the inner housing to the inside of the external housing. The inner housing is preferably suspended in the middle of the first closed volume such that during squeezing the user does not experience any obstructions.
In an embodiment of the measurement device in accordance with the invention the force sensor comprises a force-sensitive resistor. The force-sensitive resistor provides for a low-power solution, because it only provides for a measurement signal when a force is applied to it. Thus in rest, no power is consumed, which increases the battery lifetime significantly.
In an embodiment of the measurement device in accordance with the invention the first closed volume is at least partially filled with a fluid or an elastic material. The fluid may be a liquid or a gas. Alternatively, the first closed volume could contain an elastic porous material, which regains its form after squeezing it, wherein the pores are filled with a fluid.
In an embodiment of the measurement device in accordance with the invention the second closed volume is at least partially filled with a further fluid for converting a pressure on the flexible membrane into a pressure applied to the force sensor. In case of using a liquid
in the second closed volume, special measures may be necessary for protection of the force sensor. Either the force sensor has to be able to tolerate contact with liquid or it has to be properly sealed.
In a second aspect, the invention relates to a readout activation system for activating reading out of the measurement device in accordance with claim 14. As a plug belongs to a socket, the readout activation system for activating the measurement device belongs to a group of embodiments of the measurement device of the invention, in particular those that comprise a switch for deactivating part of the electronic circuit.
In an embodiment of the readout activation system in accordance with claim 15 the readout activation system comprises a receiving region, such as a recess, for receiving the measurement device, and further comprises at least one magnet configured for generating a magnetic field for controlling the switching circuit for activating or deactivating the part of the electronic circuit when the measurement device is put in or taken from the receiving region, respectively. This embodiment of the readout activation system conveniently cooperates with the embodiments of the measurement device of the invention, which comprise the switch that is activated by a magnetic field.
BRIEF INTRODUCTION OF THE DRAWINGS
In the following is described an example of a preferred embodiment illustrated in the accompanying drawings, wherein:
Fig. 1 shows an exploded view of an embodiment of the measurement device in accordance with the invention;
Fig. 2 shows an enlarged cross-sectional view of part of the measurement device of
Fig. 1 ;
Figs. 3a-3c illustrate some aspects of the functioning of the measurement device of the invention;
Figs. 4a-4d illustrate some other aspects of the functioning of the measurement device of the invention;
Figs. 5a-5c illustrate an embodiment of a readout activation system and a readout system for reading out said measurement device in accordance with the invention; and illustrates the operation of the readout activation system.
DETAILED DESCRIPTION OF THE EMBODIMENTS
The present invention relates to a measurement device for detecting and measuring pain, distress, or other discomfort of a user. The core of this measurement device is a pressure registration unit for registration of the pressure, which a user applies to the unit. The pressure registration unit will preferably be arranged to be able to register pressure in combination with time, such that it may be registered, for instance, when the user applies pressure to the unit, for how long the user applies the pressure, and how much pressure is applied. The pressure registration unit according to the invention can be used for instance in the fields of medicine, psychiatry, child welfare, and similar fields. The invention can be of a size which fits into the hand of the user. The purpose of the invention is to help the user and their therapist (or similar) to register for instance chronic pain, fear, withdrawal symptoms, and so on. Reference is made to US2013/0046205 for more background information and explanation on using such device and why it is beneficial.
Fig. 1 shows an exploded view of an embodiment of the measurement device 100 in accordance with the invention. The measurement device 100 comprises an external housing 110 having flexible walls 110w. The external housing 110 defines (alternatively the words "encloses or isolates" could be used in this context) a first closed volume 105. In Fig. 1 it is shown that the housing 110 comprises two parts 10a, 110b that are mounted together (through gluing, screwing, clamping, or the like). The measurement device 100 further comprises an internal housing 150, which is suspended within the external housing 110 by means of a positioning member 125 as shown. As the external housing is flexible, the positioning member 125 is preferably also flexible. When the respective parts 110a, 110b of the external housing are mounted together, they effectively hold the positioning member 25 in place. The internal housing 150 comprises a first part 151 , which may be non- flexible or at least much less flexible than the external housing 110. The first part 151 of the internal housing partially defines a first space 155, which comprises a force sensor 170, which preferably is a force-sensitive resistor (FSR), because of its low power consumption advantage. The first space 155 is further sealed off by a flexible membrane 152,
which in this embodiment is to be clicked over said first part 151 of the internal housing 150 and held in place with an O-ring 160, as illustrated. The membrane 152 in this embodiment is provided with a protruding element 152p, which is advantageous as discussed in the introduction of this specification.
Fig. 2 shows an enlarged cross-sectional view of the part of the measurement device of Fig. 1. In the figure, the flexible membrane 152 has been mounted on the first part 151 of the internal housing 150. By mounting said flexible membrane 152, the second closed volume 155 (earlier mentioned first space) is formed. It is illustrated how the flexible membrane 152 faces the first closed volume 105 on a first side 152s1 thereof, and the force sensor 170 on a second, opposite, side 152s2 thereof. The figure further illustrates that there is a gap 152d between said protruding part 152p and the force sensor 170. Another aspect that Fig. 2 illustrates is the amplification of the pressure/force applied to the membrane 152. The pressure in the first closed volume 105 presses on an area 152a with the size as illustrated by the arrow. Under this pressure the membrane 152 may bend towards the force sensor 170. As soon as the protruding element 152p of the membrane touches the force sensor 170 it is the contact area 152pa of the protruding element 152p, as illustrated by the other arrow, which will transfer the force to the force sensor 170. This force/pressure is effectively an amplified version of the force applied to the membrane 152. The amplification factor is typically in the order of the ratio between the membrane area 152a and the contact area 152pa of the protruding element 152.
Fig. 2 further illustrates that the force sensor 170 is connected to a printed-circuit board (PCB) 180 via a connecting wire (or wires) 171. The PCB 180 is provided in a second space 181 of the internal housing 150 as illustrated. The PCB 180 is provided with en electronic circuit 182 (i.e. an integrated circuit), which may comprise a processor or control unit for controlling and reading out the force sensor 170 and storage circuitry for storing said measurements). The electronic circuit 182 in this embodiment also comprises a switching circuit 184 and a communication circuit 186. The communication circuit 186 may be a Bluetooth transceiver circuit, which as such is well-known to the person skilled in the art. The electronic circuit is power by a battery 190. The switching circuit 184 has been added to facilitate deactivating part of the electronic circuit 182, in particular the communication circuit 186, for reasons as earlier discussed, i.e. save power and thereby increase battery lifetime.
Figs. 3a-3c illustrate some aspects of the functioning of the measurement device of the invention. In Fig. 3a the hand 200 of the user applies the so-called threshold pressure to
the measurement device 100. in this situation the flexible membrane 152, or the protruding element 152p if present, barely touches the force sensor 170, i.e. it begins to apply a small force when the force applied to the measurement device 100 is further increased. Fig. 3b shows the situation where the user applies a medium force to the measurement device. In this situation the flexible membrane 152, or the protruding element 152p if present, applies a force to the force sensor 170. Fig. 3c shows the situation where the user applies a maximum force to the measurement device. With "maximum force" it is meant the maximum force that can be registered, not the maximum force that could be applied. The force sensor 170 in this situation outputs its maximum signal level to the electronic circuit 180.
Figs. 4a-4d illustrate some other aspects of the functioning of the measurement device of the invention. Fig. 4a shows the equilibrium situation, where the user does not apply a pressure to the measurement device 100. Consequently, the membrane 152 applies a zero force F0 to the force sensor 170 (although there is still the pressure in the 155 second closed volume, which applies a pressure on the force sensor 170). Fig. 4b shows the situation which complies with Fig. 3a. A minimum force Fmn is applied to the force sensor 170. Fig. 4c shows the situation that complies with Fig. 3b. A medium force Fmd is applied to the force sensor 170. Fig. 4d shows the situation that complies with Fig. 3c. The maximum registerable force Fmx is applied to the force sensor 170. The reason for differentiating between F0 and Fmn is that the force sensor may be very sensitive (for instance when an FSR is used). Thus, in case of small pressure variations in the situation of Fig. 4a having the gap between the membrane 152 and the force sensor 170 nothing will be measured and registered by the measurement device 100. In the situation of Fig. 4b however the pressure is registered by the measurement device 100. Expressed differently, the small-signal behaviour in these two situations is very different.
Figs. 5a-5c illustrate an embodiment of a readout activation system 300 and a readout system for reading out said measurement device in accordance with the invention. The focus of the inventor has been to increase battery lifetime as much as possible. The communication circuit 182 only needs to be active when the measurement device 100 is read out by a readout system (i.e. laptop, table, PC, smartphone) 400. As discussed earlier the measurement device 100 may comprise a switching circuit for (triggering) deactivating said communication 182 (and/or other parts). In a preferred embodiment the deactivation is done in software. The measurement device 100 is configured such, that when it is put in the readout activation device 300 (also called the crib) it will broadcast and be ready for connection for a predefined time, for instance 30 seconds. After this time has lapsed,
the measurement device 100 will return to its sleep mode again (arranged in software) even if the measurement device 100 remains in the crib 300.
In Fig. 5a there is provided the readout activation system 300, which comprises in this embodiment a receiving region 310 (such as a recess) for receiving the measurement device 100 in accordance with the invention. When for example Bluetooth technology is used for wireless communication, the readout activation system 300 is preferably put within Bluetooth communication reach of the readout system 400. In Fig. 5b the measurement device 100 is put into the recess 310. In Fig. 5c the measurement device 100 is activated by the readout activation system 300 and transmits its registered data to the readout system 400 via a wireless communication signal 999 as schematically illustrated. The registered data may be shown on the readout system 400 in the form of a graph 410 for example. The physician may subsequently interpret the registered data, which forms an indication of the pain, distress or other discomfort of the user over a certain period.
Fig. 6 illustrates the operation of the readout activation system 300. This figure is very schematic in order to facilitate understanding of the principle. Near the recess 310 of the readout activation device 300 there is provided a plurality (but at least one) of magnets 350 as illustrated. These could be permanent magnets, but also other magnets are possible. These magnets 350 generate a magnetic field 355, which subsequently trigger the earlier-discussed switching circuit 184 to activate the communication circuit (not shown in Fig. 6), for instance by closing or opening when the measurement device 100 is placed in the recess 310. The switching circuit 184 be used to directly switch (on or off) the respective part electronically (i.e. in hardware), but it could also be used to trigger the deactivation through software.
It must be stressed that only one embodiment of the invention has been illustrated in the figures. However, many variations of the measurement device in accordance with the invention are possible without deviating from the scope of protection as defined by the claims. It must be stressed that the protruding element of the membrane is optional, yet results in an advantage when used. In addition, the measurement device may have other forms than illustrated. Furthermore, the second closed volume may be provided outside the first closed volume if so desired, wherein the flexible membrane then effectively forms the interface between both volumes.
It should be noted that the above-mentioned embodiments illustrate rather than limit the invention, and that those skilled in the art will be able to design many alternative embodi-
merits without departing from the scope of the appended claims. In the claims, any reference signs placed between parentheses shall not be construed as limiting the claim. Use of the verb "comprise" and its conjugations does not exclude the presence of elements or steps other than those stated in a claim. The article "a" or "an" preceding an element does not exclude the presence of a plurality of such elements. The mere fact that certain measures are recited in mutually different dependent claims does not indicate that a combination of these measures cannot be used to advantage. In the device claim enumerating several means, several of these means may be embodied by one and the same item of hardware.
Claims
1. Measurement device ( 00) for detecting and measuring pain, distress, or other discomfort of a user, the measurement device (100) comprising:
an external housing (110) having at least partially flexible walls (110w) and being configured for being held and squeezed by a hand (200) of the user, wherein the external housing (110) defines a first closed volume (105), and
a force sensor (170) for detecting and measuring pressure in the first closed volume (105), c h a r a c t e r i s e d i n that the measurement device (100) further comprises an inner housing (150), wherein the inner housing (150) defines a second closed volume (155), the second closed volume (155) comprising the force sensor (170), wherein the inner housing (150) comprises a flexible membrane (152) that is placed such that the flexible membrane (152) faces the first closed volume (105) at a first side (152s1) of the flexible membrane (152) and faces the force sensor (170) at a second, opposite, side (152s2) of the flexible membrane (152), wherein the flexible membrane (152) is positioned such that there is a gap (152d) between the flexible membrane (152) and the force sensor (170) when no force is applied by the user to the external housing (110), and that at a certain predefined pressure applied by the user the flexible membrane (152) touches the force sensor (170), wherein the force sensor (170) from that instant starts to register a force.
2. The measurement device (100) according to claim 1 , wherein the flexible membrane ( 52) is provided with a protruding element (152p) at the second side (152s2), wherein the protruding element (152p) is configured for pressing on the force sensor (170) when the flexible membrane (152) is pushed towards the force sensor (170) upon the application of the force on the external housing (110) by the hand (200) of the user.
3. The measurement device (100) according to claim 2, wherein the protruding element (152p) is designed to have a contact area (152pa) when pushed to be in contact with the force sensor (170), wherein the contact area (152pa) is designed to be a predefined factor smaller than a membrane area (152a) of the flexible membrane (152).
4. The measurement device (100) according to any one of the preceding claims, wherein the measurement device (100) further comprises an electronic circuit
(182) coupled with the force sensor (170) for controlling and reading out the force sensor (170) and for storing the measurements.
5. The measurement device (100) according to claim 4, wherein the measurement device (100) further comprises a battery (190) for supplying power to the electronic circuit (182).
6. The measurement device (100) according to any one of the preceding claims, wherein the electronic circuit (182) further comprises a communication circuit (186) for communicating registered data with a readout system (400).
7. The measurement device (100) according to claim 6, wherein the electronic circuit (182) further comprises a switching circuit (184), which is configured for deactivating part (186) of the electronic circuit (182), preferably at least the communication circuit (186), during the time that the measurement device (100) is not being read out by a readout system (400), and for activating the part (186) during the time that the measurement device (100) is to be read out by the readout system (400).
8. The measurement device (100) according to claim 7, wherein the switching circuit (184) is controllable by a magnetic field (355).
9. The measurement device (100) according to any one of the preceding claims, wherein the inner housing (150) further comprises a space (181) for containing respective components other than the force sensor (170).
10. The measurement device ( 00) according to any one of the preceding claims, wherein the inner housing (150) is suspended within the first closed volume (105) of the external housing ( 10) by means of a positioning member (125) that fixes the inner housing (150) to the inside of the external housing (110).
11. The measurement device (100) according to any one of the preceding claims, wherein the force sensor (170) comprises a force-sensitive resistor.
12. The measurement device (100) according to any one of the preceding claims, wherein the first closed volume (105) is at least partially filled with a fluid or an elastic material.
13. The measurement device (100) according to claim 1 , wherein the second closed volume (155) is at least partially filled with a further fluid for converting a pressure on the flexible membrane (152) into a pressure applied (F0, Fmn, Fmd, Fmx) to the force sensor (170).
14. Readout activation system (300) for activating reading out of the measurement device (100) in accordance with claim 7 or any one of claims 8 to 13 in as far as directly or indirectly dependent on claim 7, wherein the readout activation system (300) is configured for controlling the switching circuit (184) for activating or deactivating the part (186) of the electronic circuit (182).
15. The readout activation system (300) according to claim 14 for reading out the measurement device (100) in accordance with claim 8 or any one of claims 9 to 13 in as far as directly or indirectly dependent on claim 8, wherein the readout activation system (300) comprises a receiving region (310), such as a recess, for receiving the measurement device (100), and further comprising at least one magnet (350) configured for generating a magnetic field (355) for controlling the switching circuit (184) for activating or deactivating the part (186) of the electronic circuit (182) when the measurement device (100) is put in or taken from the receiving region (310), respectively.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DK17786224.0T DK3445229T3 (en) | 2016-04-22 | 2017-04-20 | Measurement device for detecting and measuring pain |
ES17786224T ES2907947T3 (en) | 2016-04-22 | 2017-04-20 | Measuring device to detect and measure pain |
PL17786224T PL3445229T3 (en) | 2016-04-22 | 2017-04-20 | Measurement device for detecting and measuring pain |
EP17786224.0A EP3445229B1 (en) | 2016-04-22 | 2017-04-20 | Measurement device for detecting and measuring pain |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NO20160684A NO20160684A1 (en) | 2016-04-22 | 2016-04-22 | Measurement device for detecting and measuring pain |
NO20160684 | 2016-04-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2017183994A1 true WO2017183994A1 (en) | 2017-10-26 |
Family
ID=60116211
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/NO2017/050098 WO2017183994A1 (en) | 2016-04-22 | 2017-04-20 | Measurement device for detecting and measuring pain |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP3445229B1 (en) |
DK (1) | DK3445229T3 (en) |
ES (1) | ES2907947T3 (en) |
NO (1) | NO20160684A1 (en) |
PL (1) | PL3445229T3 (en) |
WO (1) | WO2017183994A1 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019204899A1 (en) * | 2018-04-25 | 2019-10-31 | Dynamic Disc Designs Corp. | Sensitivity metering system for use in patient diagnosis |
WO2023237749A1 (en) | 2022-06-10 | 2023-12-14 | Xie Yaqi | Apparatus and method for the assessment of pain |
GB2621212A (en) * | 2022-06-10 | 2024-02-07 | Xie Yaqi | Apparatus and method for the assessment of pain |
Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5157970A (en) * | 1990-10-17 | 1992-10-27 | Lewis Jr Royce C | Grasp analysis method |
US6026684A (en) * | 1998-07-17 | 2000-02-22 | Haemonetics Corporation | Active donor hand gripper for use in a blood collection apparatus |
EP0874587B1 (en) | 1996-01-02 | 2003-11-19 | Cefar Matcher AB | Apparatus for measuring pain |
WO2004103230A1 (en) | 2003-05-22 | 2004-12-02 | Medoc Ltd. | Thermal stimulation probe and method |
WO2009052100A2 (en) | 2007-10-15 | 2009-04-23 | University Of Maryland, Baltimore | Apparatus and method for use in analyzing a patient's bowel |
US20110066078A1 (en) * | 2009-09-14 | 2011-03-17 | Artann Laboratories, Inc. | Pain monitor for a patient undergoing a medical procedure |
US20110088463A1 (en) * | 2009-10-16 | 2011-04-21 | Shapiro Ronald S | Performance enhancement measurement device for joints |
EP2359747A1 (en) * | 2010-02-12 | 2011-08-24 | AIT Austrian Institute of Technology GmbH | Method for objective detection and measurement of pains |
US20130023799A1 (en) * | 2011-07-06 | 2013-01-24 | Bernhard Brinkhaus | Apparatus and method for detecting the hand force of the hand pressure |
US20130046205A1 (en) | 2009-12-28 | 2013-02-21 | Msys Ag | Device and method for detecting and measuring pain |
US20140276188A1 (en) * | 2013-03-14 | 2014-09-18 | Accendowave Inc. | Systems, methods and devices for assessing and treating pain, discomfort and anxiety |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9123638D0 (en) * | 1991-11-07 | 1992-01-02 | Magill Alan R | Apparel & fabric & devices suitable for health monitoring applications |
US20030009308A1 (en) * | 2000-06-24 | 2003-01-09 | Chris Kirtley | Instrumented insole |
US20050070812A1 (en) * | 2003-09-25 | 2005-03-31 | Donofrio William T. | Time variant vibration stimulus response for a conscious sedation system |
FR2936140B1 (en) * | 2008-09-22 | 2013-01-18 | Univ Troyes Technologie | DEVICE FOR EVALUATING AND / OR STRENGTHENING THE FORCE OF GRIPPING |
US8945010B2 (en) * | 2009-12-23 | 2015-02-03 | Covidien Lp | Method of evaluating constipation using an ingestible capsule |
CN105027035B (en) * | 2013-03-15 | 2018-09-21 | Tk控股公司 | Man-machine interface for the pressure-sensitive control in the operating environment of dispersion energy and the method using similar product |
-
2016
- 2016-04-22 NO NO20160684A patent/NO20160684A1/en not_active Application Discontinuation
-
2017
- 2017-04-20 PL PL17786224T patent/PL3445229T3/en unknown
- 2017-04-20 WO PCT/NO2017/050098 patent/WO2017183994A1/en active Application Filing
- 2017-04-20 DK DK17786224.0T patent/DK3445229T3/en active
- 2017-04-20 EP EP17786224.0A patent/EP3445229B1/en active Active
- 2017-04-20 ES ES17786224T patent/ES2907947T3/en active Active
Patent Citations (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5157970A (en) * | 1990-10-17 | 1992-10-27 | Lewis Jr Royce C | Grasp analysis method |
EP0874587B1 (en) | 1996-01-02 | 2003-11-19 | Cefar Matcher AB | Apparatus for measuring pain |
US6026684A (en) * | 1998-07-17 | 2000-02-22 | Haemonetics Corporation | Active donor hand gripper for use in a blood collection apparatus |
WO2004103230A1 (en) | 2003-05-22 | 2004-12-02 | Medoc Ltd. | Thermal stimulation probe and method |
WO2009052100A2 (en) | 2007-10-15 | 2009-04-23 | University Of Maryland, Baltimore | Apparatus and method for use in analyzing a patient's bowel |
US20110066078A1 (en) * | 2009-09-14 | 2011-03-17 | Artann Laboratories, Inc. | Pain monitor for a patient undergoing a medical procedure |
US20110088463A1 (en) * | 2009-10-16 | 2011-04-21 | Shapiro Ronald S | Performance enhancement measurement device for joints |
US20130046205A1 (en) | 2009-12-28 | 2013-02-21 | Msys Ag | Device and method for detecting and measuring pain |
EP2359747A1 (en) * | 2010-02-12 | 2011-08-24 | AIT Austrian Institute of Technology GmbH | Method for objective detection and measurement of pains |
US20130023799A1 (en) * | 2011-07-06 | 2013-01-24 | Bernhard Brinkhaus | Apparatus and method for detecting the hand force of the hand pressure |
US20140276188A1 (en) * | 2013-03-14 | 2014-09-18 | Accendowave Inc. | Systems, methods and devices for assessing and treating pain, discomfort and anxiety |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2019204899A1 (en) * | 2018-04-25 | 2019-10-31 | Dynamic Disc Designs Corp. | Sensitivity metering system for use in patient diagnosis |
WO2023237749A1 (en) | 2022-06-10 | 2023-12-14 | Xie Yaqi | Apparatus and method for the assessment of pain |
GB2621212A (en) * | 2022-06-10 | 2024-02-07 | Xie Yaqi | Apparatus and method for the assessment of pain |
Also Published As
Publication number | Publication date |
---|---|
EP3445229B1 (en) | 2021-12-15 |
NO20160684A1 (en) | 2017-10-23 |
ES2907947T3 (en) | 2022-04-27 |
EP3445229A4 (en) | 2019-11-13 |
EP3445229A1 (en) | 2019-02-27 |
PL3445229T3 (en) | 2022-03-28 |
DK3445229T3 (en) | 2022-03-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
TWI580233B (en) | A system with separate computing units | |
JP6740344B2 (en) | Smart menstrual cup and method for measuring menstrual blood using smart menstrual cup | |
US10987044B2 (en) | Uroflowmetry systems, devices and methods | |
EP3445229B1 (en) | Measurement device for detecting and measuring pain | |
US9750456B2 (en) | Method and system of attachment and detection of attachment of a wearable sensor to clothing material | |
US9685802B1 (en) | Detection of accessory presence and orientation | |
US20060258916A1 (en) | Device for monitoring the condition of a human being | |
US20150051472A1 (en) | Card type electrocardio measuring device | |
KR102173725B1 (en) | Apparatus and Method for measuring physiological signal | |
JP2009160373A (en) | Physiological condition measuring device | |
TW201438663A (en) | Physiology signal sensing device | |
JP2013132518A (en) | Liquid detection system | |
WO2017020522A1 (en) | Control method for wearable device execution module, and wearable device | |
JP2007209430A (en) | Exercise measuring device | |
CN106955093B (en) | Physiological state monitoring device | |
JP2023509612A (en) | wearable device | |
KR20160002493U (en) | Wearable healthcare apparatus | |
US10182761B2 (en) | Method and system of attachment and detection of attachment of a wearable sensor to clothing material | |
KR20170110926A (en) | Body temperature measuring device | |
CN102661805A (en) | Electronic thermometer and information processing system | |
KR101877495B1 (en) | Smart menstrual cup and method of measuring menstrual blood by using the smart menstrual cup | |
KR20140145515A (en) | Apparatus for estimating elasticity of skin | |
KR101450999B1 (en) | Multi bio signal sensor | |
KR102069993B1 (en) | Smart menstrual cup | |
CN204723052U (en) | A kind of without button intelligent cardiac measuring device |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2017786224 Country of ref document: EP |
|
ENP | Entry into the national phase |
Ref document number: 2017786224 Country of ref document: EP Effective date: 20181122 |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 17786224 Country of ref document: EP Kind code of ref document: A1 |