US20200253507A1 - Measuring user respiration at extremities - Google Patents

Measuring user respiration at extremities Download PDF

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Publication number
US20200253507A1
US20200253507A1 US16/275,153 US201916275153A US2020253507A1 US 20200253507 A1 US20200253507 A1 US 20200253507A1 US 201916275153 A US201916275153 A US 201916275153A US 2020253507 A1 US2020253507 A1 US 2020253507A1
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Prior art keywords
user
impedance
arm
contact
contacts
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US16/275,153
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Alex Jones
Chad Vardas
Alejandro Jimenez
Jan Niewiadomski
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Vardas Solutions LLC
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Vardas Solutions LLC
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Priority to US16/275,153 priority Critical patent/US20200253507A1/en
Priority to PCT/US2019/018624 priority patent/WO2020167323A1/en
Priority to US16/284,955 priority patent/US10674939B1/en
Publication of US20200253507A1 publication Critical patent/US20200253507A1/en
Abandoned legal-status Critical Current

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/08Detecting, measuring or recording devices for evaluating the respiratory organs
    • A61B5/0816Measuring devices for examining respiratory frequency
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/05Detecting, measuring or recording for diagnosis by means of electric currents or magnetic fields; Measuring using microwaves or radio waves 
    • A61B5/053Measuring electrical impedance or conductance of a portion of the body
    • A61B5/0531Measuring skin impedance
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/68Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
    • A61B5/6801Arrangements 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
    • A61B5/6802Sensor mounted on worn items
    • A61B5/681Wristwatch-type devices
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/72Signal processing specially adapted for physiological signals or for diagnostic purposes
    • A61B5/7225Details of analog processing, e.g. isolation amplifier, gain or sensitivity adjustment, filtering, baseline or drift compensation
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61BDIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00Measuring for diagnostic purposes; Identification of persons
    • A61B5/72Signal processing specially adapted for physiological signals or for diagnostic purposes
    • A61B5/7271Specific aspects of physiological measurement analysis
    • A61B5/7278Artificial waveform generation or derivation, e.g. synthesising signals from measured signals

Definitions

  • the present disclosure relates to the field of sensors, including, more particularly, to methods and systems for measuring a user's respiration.
  • Heart Rate Variability is the variation of the time intervals between heart beats.
  • An increase in HRV is desirable because it is indicative of a heart rate that is variable and responsive to physiological demands.
  • HRV is greatest when individuals breathe at a frequency that is particular to that individual—their resonance breathing frequency (or “resonance breathing rate”).
  • Respiratory Sinus Arrhythmia RSA
  • Heart Rate Variability HRV is in synchrony with respiration, shown when variability on an ECG is shortened during inspiration (“inhalation”) and prolonged during expiration (“exhalation”).
  • Some existing systems and methods for measuring a user's respiration rate rely on a change in the impedance of the user's chest. That change in impedance is caused by two aspects of a user's respiration: a change in the volume of gas in relation to the surrounding tissue; and a change in the electrical path length across the chest that is caused by the expansion of the chest.
  • the impedance increases as the gas volume and path length increase.
  • electrodes may be placed on the user on either side of the chest and modulation signals (excitation signals of an alternating current signal at a known frequency) may be passed between the electrodes.
  • modulation signals excitation signals of an alternating current signal at a known frequency
  • a respiration voltage signal is imposed on the base voltage signal by the increase in impedance caused by the user's respiration.
  • the resulting combined voltage signal is demodulated.
  • the respiration frequency is determined from the resulting demodulated voltage signal.
  • FIG. 1 is a prior art circuit diagram for a Texas Instruments ADS1292R from the data sheet for the Texas Instruments ADS1292R, which is a low-power, 2-channel, 24-bit analog-to-digital converter.
  • the datasheet for a Texas Instruments ADS1292R discloses that a feature of the ADS1292R is an integrated respiration impedance measurement.
  • FIG. 1 depicts FIG. 56 from the data sheet for the TI ADS1292R.
  • the pin assignments from the ADS1292R are provided in TABLE 1.
  • the modulation signals are supplied by RESP_MODP and RESP_MODN.
  • Exemplary modulation frequencies are 32 kHz and 64 kHz.
  • the two leads are each wired into channel 1 for respiration signals and channel 2 for ECG signals.
  • FIG. 1 depicts the Right Arm Lead wired into IN2N and IN1N and the Left Arm Lead wired into IN1P and IN2P.
  • FIG. 1 further depicts that the Right Arm Lead is also wired into RESP_MODP and that the Left Arm Lead is also wired into RESP_MODP.
  • FIG. 1 is a prior art circuit diagram
  • FIG. 2 is a circuit diagram illustrating aspects of an embodiment of a system for measuring the respiration of a user
  • FIG. 3 is a circuit diagram further illustrating aspects of the embodiment of a system for measuring the respiration of a user of FIG. 2 ;
  • FIG. 4 illustrates an embodiment of a method for measuring the respiration of a user
  • FIG. 5 illustrates an embodiment of a method for measuring the respiration of a user
  • FIG. 6 illustrates an embodiment of a method for measuring the respiration of a user
  • FIG. 7 illustrates an embodiment of a method for measuring the respiration of a user
  • FIG. 8 is a simplified, exemplary block diagram of an embodiment of a system for measuring the respiration of a user
  • FIG. 9 is an exemplary block diagram of a computing device from the system of FIG. 8 ;
  • FIG. 10 includes front, back, top, bottom, and right views of an embodiment of a biometric analysis device implementing embodiments of the systems and methods disclosed herein;
  • FIG. 11 is a perspective view of the biometric analysis device of FIG. 10 .
  • Applicant desired to measure a user's respiration and ECG signals at the user's wrist using a wrist-mounted device.
  • the circuit disclosed in the data sheet for the TI ADS1292R was unsatisfactory for measuring a user's respiration at this extremity because excessive electromagnetic interference (EMI) resulted in noise in the demodulated signal.
  • EMI electromagnetic interference
  • the noise was large enough to cause errors in the determination of a user's respiration rate.
  • Applicant surmised that the ability of the human body to act as an antenna contributed to the excessive EMI and that attempting to measure respiration from an extremity (i.e., the wrist) further exacerbated the EMI.
  • Embodiments within disclose improved systems and methods for measuring respiration that are suitable for measuring respiration at the user's extremities.
  • the embodiments are discussed using the Texas Instruments ADS1292R processor, but the ADS1292R is an exemplary electronics device and the systems and methods disclosed within may be practiced using other processors, processor sets, circuitry (both digital and analog), or combinations of these.
  • processing electronics may include one or more processors, processor sets, circuitry (both digital and analog), or combinations of these.
  • the improvements may include one or more of the following: 1) providing user-excitation contacts for the AC modulation signals where the user-excitation contacts are separate and distinct from user impedance-measuring contacts; 2) adding a low-pass filter between each user impedance-measuring contact and the respective input into the processing electronics; 3) adding a capacitance between the inputs into the processing electronics; 4) filtering a digital impedance signal within the processing electronics to remove a DC component; 5) filtering the digital impedance signal within the processing electronics with a low-pass filter to remove further noise; and 6) creating long and short running averages of the impedance signal and, from these, determining that the user is inhaling when the short running average is greater than the long running average and that the user is exhaling when the short running average is less than the long running average.
  • FIG. 2 and FIG. 3 are circuit diagrams illustrating aspects of an embodiment of a system for measuring a user's respiration from extremities.
  • FIG. 2 illustrates an embodiment of a modulation circuitry 200 , which provides user-excitation contacts for the AC modulation signals that are separate and distinct from user impedance-measuring contacts that are wired into the respiration channel of processing electronics 201 . It was determined that providing contacts for the AC-modulation signals that are separate from the impedance-measuring contacts, by itself, significantly reduced noise (e.g., due to EMI) in the impedance measurement.
  • FIG. 1 illustrates an embodiment of a modulation circuitry 200 , which provides user-excitation contacts for the AC modulation signals that are separate and distinct from user impedance-measuring contacts that are wired into the respiration channel of processing electronics 201 . It was determined that providing contacts for the AC-modulation signals that are separate from the impedance-measuring contacts, by itself, significantly reduced noise (e.g.,
  • modulation circuitry 200 includes a first user-excitation contact (RL) 202 coupled to a respiration modulation excitation signal source 206 from electronics 201 (e.g., a TI ADS1292R) through a capacitance and a resistance 218 .
  • the capacitance includes a first capacitor 210 and a second capacitor 214 .
  • a second user-excitation contact (LL) 204 is coupled to a respiration modulation excitation signal source 208 through a capacitance and a resistance 220 .
  • the capacitance includes a first capacitor 212 and a second capacitor 216 .
  • FIG. 1 first user-excitation contact
  • user-excitation contacts 202 and 204 are placed in contact with the skin of a user and on either side of the user's chest.
  • a contact may be made, e.g., at each wrist of the user, or at one wrist and a finger of the opposing arm.
  • Exemplary modulation frequencies for the user-excitation signals include 32 kHz and 64 kHz.
  • resistances 218 , 220 may be 40 k ⁇
  • capacitors 210 , 212 may be 100 nF
  • capacitors 214 , 216 may be 2200 pF.
  • FIG. 3 is a circuit diagram further illustrating aspects of the embodiment of a system for measuring a user's respiration from extremities of FIG. 2 .
  • FIG. 3 illustrates circuitry 300 , which includes circuitry for measuring the impedance of a user at extremities using a first user-extremity contact 302 and a second user-extremity contact 304 .
  • user-extremity contacts 302 and 304 are placed in contact with the skin of the user and on either side of the user's chest.
  • a contact may be made, e.g., at each wrist of the user, or at one wrist and a finger of the opposing arm.
  • modulation circuitry 200 is completely separate and distinct from the impedance-measuring circuitry between user contacts 302 , 304 up to electronics 201 .
  • user-extremity contact 302 is coupled to an impedance-measuring input 310 to electronics 201 .
  • input 310 is differential analog negative input 1 to the TI ADS1292R.
  • Second user-extremity contact 304 is coupled to a second input 312 to electronics 201 .
  • input 312 is differential analog positive input 1 to the TI ADS1292R.
  • the circuitry further includes a capacitance, voltage biasing circuitry, and a low-pass filter 318 .
  • the capacitance includes two capacitors 342 , 344 .
  • the voltage biasing circuitry includes two resistors 350 , 352 , each coupled at one end between the capacitance and low-pass filter 318 , with resistor 350 coupled to an analog supply voltage 340 and resistor 352 coupled to an analog ground 338 .
  • low-pass filter 318 includes a resistor 330 coupled between the voltage biasing circuitry and input 310 and includes a capacitor 332 coupled between resistor 330 and input 310 at one end and to ground 338 at the other.
  • the circuitry mimics that between contact 302 and input 310 , further including a capacitance, voltage biasing circuitry, and a low-pass filter 320 .
  • the capacitance includes two capacitors 346 , 348 .
  • the voltage biasing circuitry includes two resistors 354 , 356 , each coupled at one end between the capacitance and low-pass filter 320 , with resistor 354 coupled to an analog supply voltage 340 and resistor 356 coupled to an analog ground 338 .
  • low-pass filter 320 includes a resistor 334 coupled between the voltage biasing circuitry and input 312 and includes a capacitor 336 coupled between resistor 334 and input 312 at one end and to ground 338 at the other.
  • the series capacitance (e.g., capacitors 342 , 344 and 346 , 348 ) prevents a potential DC current being applied to the user, with the redundancy of two capacitors protecting against the short-circuiting of one of the capacitors.
  • the voltage-biasing circuitry establishes a pre-determined voltage between the two resistors (e.g., between resistors 350 and 352 and between resistors 354 and 356 ) that, in this embodiment, is half-way between analog ground 338 and analog supply voltage 340 .
  • Low-pass filters reduce EMI significantly, which contributes to the ability of the embodiment to measure a user's respiration when user-contacts 302 , 304 are placed on the user's extremities.
  • Embodiments may further include a capacitance between the impedance-sensing inputs to the electronics that is sized to reduce DC noise. In FIG. 3 , such a capacitance is represented by a capacitor 358 coupled between inputs 310 and 312 .
  • the elements of circuit 300 may have the following values: capacitors 342 , 346 may be 100 nF; capacitors 344 , 348 may be 2200 pF; resistors 350 , 352 , 354 , 356 may be 10 M ⁇ ; resistors 330 , 334 may be 220 k ⁇ ; capacitors 332 , 336 may be 22 pF; and capacitor 358 may be 10 pF.
  • low-pass filters 318 , 320 have cut-off frequencies 32.9 kHz.
  • low-pass filters 318 , 320 may have other cut-off frequencies and still reduce EMI sufficiently to allow measuring a user's respiration at extremities.
  • the cut-off frequencies of low-pass filters 318 , 320 are chosen to narrow the band that must be filtered later by digital filters within electronics 201 . By narrowing the band, digital filters with better response may be chosen.
  • the cut-off frequencies may be between thirty and thirty-five kilohertz.
  • low-pass filters 318 , 320 work in combination with signal-processing logic within electronics 201 to even further reduce EMI because low-pass filters 318 , 320 may have cut-off frequencies determined to work synergistically with signal-processing logic within electronics 201 .
  • low-pass filters 318 , 320 have cut-off frequencies chosen to reduce relatively high-frequency EMI, e.g., EMI frequencies of from 100 kHz to 1000 kHz, and the digital filtering discussed within is directed to filtering out substantially lower frequencies, e.g., with cutoff frequencies of from 0.4 Hz to 20 Hz.
  • the hardware low-pass filters 318 , 320 filter out most of the noise that comes from the user's body to the circuit and the digital filters within electronics 201 may then be optimized (e.g., with filters that have improved response times) to address board noise of substantially lower frequencies, primarily 24 Hz and 60 Hz.
  • the two different low pass filtering systems work together to provide a usable respiration signal. Further smoothing of that signal is applied digitally as discussed within, e.g., regarding FIGS. 4-7 .
  • FIG. 3 further illustrates an embodiment of a system for measuring a user's ECG at extremities. For reasons that are similar to those when measuring respiration at extremities, measuring a user's ECG at extremities suffers from increased EMI.
  • circuitry 300 illustrates an embodiment of ECG-measuring circuitry for measuring the impedance of a user at extremities using first user-extremity contact 302 and second user-extremity contact 304 when user contacts 302 , 304 are placed in contact with the skin of the user and on either side of the user's chest, e.g., at each wrist of the user, or at one wrist and a finger of the opposing arm.
  • FIG. 3 further illustrates an embodiment of a system for measuring a user's ECG at extremities. For reasons that are similar to those when measuring respiration at extremities, measuring a user's ECG at extremities suffers from increased EMI.
  • circuitry 300 illustrates an embodiment of ECG-measuring circuitry for measuring the impedance of a user
  • a low-pass filter 314 is coupled between user-extremity contact 302 and an input 306 to electronics 201 .
  • input 306 is differential analog negative input 2 to the TI ADS1292R chip.
  • Low-pass filter 314 includes a resistor 322 coupled between user contact 302 and input 306 and includes a capacitor 324 coupled between resistor 322 and input 306 at one end and to ground 338 at the other.
  • low-pass filter 316 including a resistor 326 coupled between user contact 304 and input 308 and includes a capacitor 328 coupled between resistor 326 and input 308 at one end and to ground 338 at the other.
  • low-pass filters 314 , 316 have cutoff frequencies that are chosen for anti-aliasing the signals to inputs 306 , 308 , which means their cutoff frequencies are substantially higher than those of low-pass filters 318 , 320 .
  • the cutoff frequencies of low-pass filters 314 , 316 may be 60,000 Hz.
  • electronics 201 includes instructions, which, when contacts 202 , 204 , 302 , 304 are in contact with a user, cause electronics 201 to determine the impedance between user extremity contacts 302 and 304 and measure the user's respiration rate. The instructions are further discussed regarding FIGS. 4-7 .
  • electronics 201 may include a first processor and a second processor.
  • the first processor includes electronics contacts 206 , 208 , 310 , 312 .
  • the first processor creates a digital impedance signal corresponding to analog impedance data from user contacts 302 , 304 and provides the digital impedance signal to the second processor for subsequent digital signal processing.
  • the first processor may be a TI ADS1292R analog-to-digital converter and the second processor may be an Arm Cortex M4.
  • FIG. 4 illustrates an embodiment of a method 400 for measuring a user's respiration from an extremity of the user.
  • method 400 is performed with first and second user contacts on opposing sides of the user's chest and the third and fourth user contacts also on opposing sides of the user's chest.
  • an AC current is provided between first and second user contacts, causing an impedance to develop between third and the fourth user contacts.
  • the contacts may be at a user's extremity, e.g., a user's wrist, or a user's finger.
  • the impedance is detected between the third and the fourth user contacts, the impedance changing with time due to the respiration of the user.
  • a signal is created that may be used to indicate the respiration rate of the user.
  • the signal is created, in part, by demodulating the detected impedance to separate the contribution from the user's respiration from the contribution from the AC modulation signal.
  • step 416 at least one step from the following steps may be performed: the signal is stored in memory; the signal is displayed with an electronic device, and the signal is provided to a processor for further processing.
  • steps 410 - 416 may be performed using an embodiment of a system described in FIG. 2 and FIG. 3 , with the embodiment providing a signal indicating a respiration rate of the user and benefitting from noise-reduction contributions provided by embodiments of the system described regarding FIG. 2 and FIG. 3 .
  • FIG. 4 indicates additional steps, one or more of which may be added between steps 412 and 414 to assist in creating the signal that may be used to indicate the respiration rate of the user.
  • an impedance signal may be created from the impedance detected in step 412 between the third and the fourth user contacts.
  • the impedance signal may be filtered to remove a DC component, which was determined to exist even after demodulation.
  • the filtering to remove a DC component may use a digital filter.
  • the digital filter may be an infinite impulse response (IIR) filter for DC current with a filtering constant of 0.992.
  • IIR infinite impulse response
  • the impedance signal may be filtered through a low-pass filter, e.g., to further remove EMI.
  • the low-pass filter may be a digital filter.
  • the digital low-pass filter may be a finite impulse response (FIR) low-pass filter.
  • the filter is chosen to permit frequencies associated with breathing rates, including the particularly desired (or “targeted”) breathing rates.
  • the FIR may be a 179 th order filter with a gain of 1 with 5 dB from 0 to 0.5 Hz and a gain of 0 from 3 Hz and above and with ⁇ 40 dB attenuation.
  • the FIR may be a 179 th order filter with a gain of 1 with 5 dB from 0 to 2 Hz and a gain of 0 from 3 Hz and above and with ⁇ 40 dB attenuation.
  • the impedance signal may be filtered by a band-pass filter.
  • the band-pass filter may be a digital filter.
  • the digital band-pass filter may be a combination of the IIR filter for DC current and the FIR low-pass filter.
  • steps 420 , 422 are effective in reducing noise in the impedance measurement, both individually and in combination.
  • steps 420 , 422 may be performed with steps 410 - 416 to provide a signal indicating a respiration rate of the user and benefitting from noise-reduction contribution from each added step.
  • steps 410 - 416 may be performed using an embodiment of a system described in FIG. 2 and FIG. 3 , with the embodiment of method and system providing a signal indicating a respiration rate of the user and benefitting from the noise-reduction contributions of step 420 or step 422 or both.
  • FIG. 5 illustrates an embodiment of a method 500 for measuring a user's respiration from extremities.
  • FIG. 500 describes steps that may be performed on an impedance signal created from the detected impedance between the third and fourth user contacts (as in any of the signals created in steps 412 , 418 , 420 , or 422 , before they are provided to step 414 ) from which a signal indicting a respiration rate of the user is created as in step 414 .
  • step 502 from an impedance signal created from the time-varying impedance detected between the third and fourth user contacts, a first running average is created over a first running period of time.
  • step 504 from the same impedance signal of step 502 , a second running average is created from a second running period of time, where the second running period of time is substantially shorter than the first running period of time.
  • step 506 the first and second running averages are compared and if the second running average is greater than the first, it is determined that the user is inhaling. Conversely, in step 508 , if the second running average is less that the first, it is determined that the user is exhaling.
  • step 510 the durations of time between the determinations of when the user is inhaling and exhaling are used to create the signal indicating the respiration rate of the user.
  • the longer running average is taken over a period of time with a duration sufficient to determine the average impedance of at least one entire wave, i.e., an entire respiration cycle. This effectively provides the center amplitude of the wave (or the “baseline”).
  • taking the longer running average is a form of a DC component filtering over and above the IIR filter mentioned earlier.
  • the shorter running average is taken over a period of time with a duration that reduces noise without filtering out the impedance change caused by the user's respiration.
  • the shorter running average is taken over a 2-second window and the longer running average is taken over an 11-second window.
  • the shorter running average is also a form of filtering that is over and above the FIR filter mentioned earlier.
  • the methods discussed regarding FIG. 4 , or FIG. 5 , or both, may be performed by embodiments of systems discussed regarding FIG. 2 and FIG. 3 .
  • the methods of FIG. 4 and FIG. 5 may be performed by electronics 201 where electronics 201 includes a first processor and a second processor.
  • the first processor includes electronics contacts 206 , 208 , 310 , 312 .
  • the first processor creates a digital impedance signal corresponding to analog impedance data from user contacts 302 , 304 and provides the digital impedance signal to the second processor for subsequent digital signal processing.
  • the first processor may be a TI ADS1292R analog-to-digital converter and the second processor may be an Arm Cortex M4.
  • the filtering power of low-pass filters 318 , 320 is increased (or the filtering is “front loaded”), which allows the digital filtering described regarding FIG. 4 and FIG. 5 to be fine-tuned and directed to the remaining noise, thus enhancing the overall noise-reducing effect of the embodiment over changes to just the circuits 200 , 300 or to just the methods 400 , 500 .
  • FIG. 6 illustrates an embodiment of a method 600 for measuring the respiration of a user.
  • the embodiment of FIG. 6 is directed to processing that may be performed on a digital signal created from the changes in impedance caused by a user's respiration, e.g., a digital signal created from the impedance from step 412 of method 400 , or a digital impedance signal created by electronics 201 and further processed by software within electronics 201 .
  • a data point indicative of an impedance is received (or taken) at a pre-determined frequency, e.g., every 2 ms (i.e., the sampling rate is 500 Hz).
  • a pre-determined number of data points are summed, e.g., 10 data points may be summed.
  • a filter is implemented that produces a filtered data point at a predetermined frequency, e.g., every 20 ms (i.e., 50 Hz).
  • a single-order IIR filtering is performed on the data from step 606 to reduce DC noise.
  • this IIR filter is an IIR filter from Texas Instruments included with the TI ADS1292R digital-to-analog converter.
  • step, 610 the data stream from step 608 is further filtered using a low-pass FIR filter, e.g., a 179 th -order low-pass FIR filter with a cut-off frequency of 0.4 Hz.
  • a low-pass FIR filter e.g., a 179 th -order low-pass FIR filter with a cut-off frequency of 0.4 Hz.
  • an FIR filter may be employed with such a low cut-off frequency without the number of taps being too large for the processor to accommodate (i.e., a lower-order FIR filter).
  • a running average e.g., a 10-sample running average, is used to smooth the output from the FIR filter and prepare the data for a differentiation filter.
  • step 614 the data is filtered with a differentiation filter, e.g., a 5 th -order differentiation filter, which removes high-frequency components from the data. If the output of step 614 is larger than 0, then the user is determined to be inhaling. Otherwise the user is exhaling.
  • step 616 the data is integrated using a moving window integrator with, e.g., a 50-sample window, which at this sampling rate is 1 second of data. The output of step 616 may be used to compare the phase angle of the user's respiration with a target respiration. In an embodiment, the user's respiration rate may be determined using the time between zero-transitions with the data from step 614 .
  • a differentiation filter e.g., a 5 th -order differentiation filter
  • the determined user respiration rate may be compared to the changes in the user's HRV to determine whether the user's HRV is in synchrony with the user's respiration (i.e., whether the user is in RSA).
  • the signal from step 412 may be processed as described in steps 608 - 614 with the resulting signal supplied to step 414 .
  • the signal from step 412 may be processed as described in steps 602 - 614 with the resulting signal supplied to step 414 .
  • FIG. 7 illustrates an embodiment of a method 700 for measuring the respiration of a user that corrects for (or “cancels out”) skewing that might be induced due the user's skin varying in a level of moistness while respiration is being measured.
  • Method 700 builds on method 600 .
  • the zeroes in the differentiation-filtered output of step 614 are used to find the local minimums and maximums of the user's respiration.
  • a running average is created from the local minimums and a running average is created from the local maximums.
  • the output of step 614 is rescaled by dividing positive values by the running average of the local maximums and by dividing negative values by the running average of the local minimums.
  • step 706 The result of step 706 is that the respiration data will be a scaled wave that ranges from ⁇ 1 to 1, where positive values indicate the user is inhaling and negative values indicate the user is exhaling. With the respiration data being maintained between ⁇ 1 and 1, the skew is eliminated.
  • the running average of step 704 is constructed using the last ten (10) local minimums and last ten (10) local maximums.
  • FIG. 8 is a simplified, exemplary block diagram of an embodiment of a system 800 for implementing the embodiments of systems and methods disclosed herein.
  • System 800 may include a number of sensors, e.g., a respiration rate sensor 805 (e.g., as described within this disclosure) and a heart rate sensor 810 (e.g., as described within this disclosure), for developing data regarding a user.
  • Sensors 805 , 810 , and 820 are in communication with a computing device 815 .
  • Computing device 815 may further be in control of a haptic device 825 and a buzzer or speaker (not shown) for communicating with the user.
  • System 800 may be referred to as a Biometric Analysis Device.
  • Respiration rate sensor 805 may be an impedance-based sensor as discussed within this specification.
  • Heart rate sensor 810 may be, e.g., a plurality of sensors sufficient to produce an electrocardiogram (ECG, as discussed within), a chest-mounted device, or a wrist-mounted device, so long as the device provides heart rate data with sufficient accuracy and precision.
  • Sensor 820 is representative of additional sensors that may be included, such as sensors for determining galvanic skin response, temperature, blood pressure, hydration, sleep, exercise activity, brain activity, nutrient levels, or blood analysis. Sensors 805 , 810 , and 820 may supply data to computing device 815 via communication links 830 .
  • Computing device 815 may include a user interface and software, which may implement the steps of the methods disclosed within.
  • Computing device 815 may receive data from sensors 805 , 810 , and 820 , via communication links 830 , which may be hardwire links, optical links, satellite or other wireless communications links, wave propagation links, or any other mechanisms for communication of information.
  • Communication links 830 may be hardwire links, optical links, satellite or other wireless communications links, wave propagation links, or any other mechanisms for communication of information.
  • Various communication protocols may be used to facilitate communication between the various components shown in FIG. 8 .
  • Distributed system 800 in FIG. 8 is merely illustrative of an embodiment and does not limit the scope of the systems and methods as recited in the claims.
  • the elements of system 800 are incorporated into a single, wearable Biometric Analysis Device (e.g., as described regarding FIGS. 10 and 11 ).
  • computing device 815 may be employed.
  • sensors 805 , 810 , and 820 may be coupled to computing device 815 via a communication network (not shown) or via some other server system.
  • Computing device 815 may be responsible for receiving data from sensors 805 , 810 , and 820 , performing processing required to implement the steps of the methods, and for interfacing with the user.
  • computing device 815 may receive processed data from sensors 805 , 810 , and 820 .
  • the processing required is performed by computing device 815 .
  • computing device 815 runs an application for receiving user data, performing the steps of the method, and interacting with the user.
  • computing device 815 may be in communication with a server, which performs the required processing, with computing device 815 being an intermediary in communications between the user and the processing server.
  • Some example computing devices 815 include desktop computers, portable electronic devices (e.g., mobile communication devices, smartphones, tablet computers, laptops) such as the Samsung Galaxy Tab®, Google Nexus devices, Amazon Kindle®, Kindle Fire®, Apple iPhone®, the Apple iPad®, Microsoft Surface®, the Palm PreTM, or any device running the Apple iOS®, Android® OS, Google Chrome® OS, Symbian OS®, Windows Mobile® OS, Windows Phone, BlackBerry® OS, Embedded Linux, Tizen, Sailfish, webOS, Palm OS® or Palm Web OS®; or wearable devices such as smart watches, smart fitness or medical bands, and smart glasses.
  • portable electronic devices e.g., mobile communication devices, smartphones, tablet computers, laptops
  • Samsung Galaxy Tab® e.g., Samsung Galaxy Tab®, Google Nexus devices, Amazon Kindle®, Kindle Fire®, Apple iPhone®, the Apple iPad®, Microsoft Surface®, the Palm PreTM, or any device running the Apple iOS®, Android® OS, Google Chrome® OS, Symbian OS®, Windows Mobile® OS, Windows
  • FIG. 9 is an exemplary block diagram of a computing device 815 from the system of FIG. 8 .
  • a user interfaces with the system through computing device 815 , which also receives data and performs the computational steps of the embodiments.
  • Computing device 815 may include a display, screen, or monitor 905 , housing 910 , input device 915 , sensors 950 , and a security application 945 .
  • Housing 910 houses familiar computer components, some of which are not shown, such as a processor 920 , memory 925 , battery 930 , speaker, transceiver, antenna 935 , microphone, ports, jacks, connectors, camera, input/output (I/O) controller, display adapter, network interface, mass storage devices 940 , and the like.
  • I/O input/output
  • sensors 950 may include sensors 805 , 810 , and 820 incorporated into computing device 815 , and haptic device 825 may also be incorporated into device 815 .
  • housing 910 is the housing of the wearable biometric analysis device 1000 of FIGS. 10 and 11 .
  • Input device 915 may also include a touchscreen (e.g., resistive, surface acoustic wave, capacitive sensing, infrared, optical imaging, dispersive signal, or acoustic pulse recognition), keyboard (e.g., electronic keyboard or physical keyboard), buttons, switches, stylus, or combinations of these.
  • a touchscreen e.g., resistive, surface acoustic wave, capacitive sensing, infrared, optical imaging, dispersive signal, or acoustic pulse recognition
  • keyboard e.g., electronic keyboard or physical keyboard
  • Display 904 may include dedicated LEDs for providing directing signals and feedback to a user.
  • Mass storage devices 940 may include flash and other nonvolatile solid-state storage or solid-state drive (SSD), such as a flash drive, flash memory, or USB flash drive.
  • SSD solid-state drive
  • Other examples of mass storage include mass disk drives, floppy disks, magnetic disks, optical disks, magneto-optical disks, fixed disks, hard disks, CD-ROMs, recordable CDs, DVDs, recordable DVDs (e.g., DVD-R, DVD+R, DVD-RW, DVD+RW, HD-DVD, or Blu-ray Disc), battery-backed-up volatile memory, tape storage, reader, and other similar media, and combinations of these.
  • SSD solid-state drive
  • Other examples of mass storage include mass disk drives, floppy disks, magnetic disks, optical disks, magneto-optical disks, fixed disks, hard disks, CD-ROMs, recordable CDs, DVDs, recordable DVDs (e.g., DVD-R, DVD+R, DVD-RW, DVD+
  • System 900 may also be used with computer systems having configurations that are different from computing device 815 , e.g., with additional or fewer subsystems.
  • a computer system could include more than one processor (i.e., a multiprocessor system, which may permit parallel processing of information) or a system may include a cache memory.
  • the computing device 815 shown in FIG. 9 is but an example of a computer system suitable for use.
  • computing device 815 is a wrist-mounted Biometric Analysis Device in communication with or incorporating the sensors of FIG. 9 .
  • An example of such a Biometric Analysis Device is discussed regarding device 1000 of FIGS. 10 and 11 .
  • Other configurations of subsystems suitable for use will be readily apparent to one of ordinary skill in the art.
  • computing device 815 is a mobile communication device such as a smartphone or tablet computer.
  • smartphones include the Droid Incredible and Google Nexus One®, provided by HTC Corporation, the iPhone® or iPad®, both provided by Apple, BlackBerry Z10 provided by BlackBerry (formerly Research In Motion), and many others.
  • the Biometric Analysis Device may be a laptop or a netbook.
  • the Biometric Analysis Device is a non-portable computing device such as a desktop computer or workstation.
  • system 900 may be incorporated into a single module.
  • the module may have four user contacts (or “electrodes”) placed to allow a user to make contact with two contacts with one user extremity and with the other two contacts with the other user extremity.
  • This module can be contained within numerous types of wristband straps (leather, etc.) and form factors (such as key chain, steering wheel cover, etc.).
  • the module, or the strap or other form factor may also include a small OLED display to display the current time.
  • the module may execute software that performs an embodiment of the method. Accordingly, the module may provide the user with feedback, e.g., an indication of the user's respiration rate or heart rate or both.
  • FIG. 10 includes front, back, top, bottom, and right views of an embodiment of a wearable biometric analysis device 1000 for implementing embodiments of the methods disclosed within. Components and capabilities of biometric analysis device 1000 are also described with reference to FIGS. 2-9 .
  • Biometric Analysis Device 1000 includes a computing device 1005 and a sensor coupled to electrical contacts 1010 , 1012 , 1014 , 1016 that acquire data that may be used to provide a measure of the user's respiration rate as discussed above.
  • Computing device 1005 processes biometric data measured by the sensor(s) and produces feedback correlating to the processed biometric data. By continuously monitoring one or more biometric values, the user may respond to the data received and modify their behavior or activity to improve health and performance.
  • the biometric analysis device 1000 thereby provides feedback by sensing and reporting a biometric value measured by the sensor to the user in real time.
  • contacts 1010 , 1012 , 1014 , 1016 provide data to a TI ADS1292R sensor.
  • Biometric Analysis Device 1000 may be equipped with both a respiration rate sensor and a heart rate sensor.
  • Computing device 1005 is in communication with the sensor or sensors associated with contacts 1010 , 1012 , 1014 , 1016 .
  • Computing device 1005 may also control a haptic device (not shown) for communicating with the user.
  • Computing device 1005 may include a display 1015 , a user interface, and software, for implementing the steps of the methods disclosed within.
  • contacts 1010 and 1012 may correspond to contacts 202 and 302 as described above, and contacts 1014 and 1016 may correspond to contacts 204 and 304 as described above.
  • a method for determining the user's respiration rate includes the user placing device 1000 on one of the user's wrists such that contacts 1010 , 1012 are in contact with the user's wrist. Then, the user brings contacts 1014 , 1016 in contact with another part of the user's body such as one or more fingers on the user's opposing hand.
  • the user touches contacts 1014 , 1016 to a part of the user's body so that some or all of the user's chest is between contact pairs 1010 , 1012 and 1014 , 1016 (the circuits are described with reference to FIGS. 2 and 3 and contact pairs 202 , 302 and 204 , 304 ).
  • the part of the user's body may be a finger or other part of the opposing arm, may be a section of the user's torso, or may be a section of a leg of the user.
  • Computing device 1005 may receive data from sensors 1010 , 1012 , 1014 , 1016 , perform processing required to implement the steps of the methods disclosed within, and provide a user interface via display 1015 . In some embodiments, all processing required is performed by computing device 1005 . In such embodiments, computing device 1005 executes instructions for receiving user data, performing the steps of the method, and interacting with the user. In other embodiments, computing device 1005 may be in communication with a server, which performs part of the required processing, with computing device 1005 being an intermediary in communications between the user and the processing server.
  • Biometric Analysis Device 1000 generally comprises a band 1020 configured to be worn about a wrist of the user.
  • the band 1020 includes an adjustment mechanism 1025 , for adjusting a circumference of the band 1020 .
  • a user can thus select, using adjustment mechanism 1025 , a particular size for positioning band 1020 about the user's wrist.
  • a visual indication e.g., for feedback, may be provided by display 1015 .
  • visual indicators may be further be positioned on the band 1020 to provide visual signals to the user.
  • Sensor(s) associated with contacts 1010 , 1012 , 1014 , 1016 may be configured to be activated by computing device 1005 .
  • additional sensors e.g., a temperature sensor or a galvanic response sensor, may be provided to provide more user data for determining vagal tone.
  • one or more translucent windows may be positioned about the band 1020 to transmit light from one or more indicators positioned with the band 1020 .
  • Biometric analysis device 1000 in one embodiment, is used measure a user's respiration rate. Accordingly, the biometric analysis device 1000 may provide the user with real-time, personal biofeedback. In an embodiment, device 1000 may measure both a user's respiration rate and heart rate and provide feedback regarding one or both. The biofeedback may allow the user to learn about the user's personal physiological state and physiological responses. As a result, the biofeedback provided to the user (by, e.g., one or more of display 1015 , or haptic device, or speaker) may enable the user to self-regulate the user's activity and behavior to improve the user's performance or health.
  • device 1000 may provide a user with feedback (e.g., a vibration pattern of frequency, duration, and magnitude) selected to encourage a desired behavior.
  • biometric analysis device 1000 is configured to provide the user with feedback with reference to previously-collected biometric data, such as respiration rate or heart rate variability.
  • the biometric analysis device 1000 may emit vibrations based on the user's actual respiration rate, or a target respiration rate.
  • a visual indication from, e.g., display 1015 may be provided and configured to emit different colors based on when the user is supposed to inhale and exhale for deep breathing relaxation techniques.
  • the user may also be capable of changing the breathing intervals.
  • the visual indication and breathing intervals may be enabled and adjusted through the user interface.
  • FIG. 11 is a perspective view of the biometric analysis device of FIG. 10 .
  • FIGS. 10 and 11 illustrate one example embodiment of a wearable biometric analysis device 1000 that is configured to measure the respiration rate of a user.
  • biometric analysis device 1000 can include each of the elements of system 800 of FIG. 8 and FIG. 9 .
  • biometric analysis device 1000 can include other elements that function with biometric analysis device 1000 to provide biometric measurement and analysis to assist a user with stress management.

Abstract

Systems and methods measure impedance across a user's chest during respiration to determine a rate of respiration. With AC-modulation contacts separated from impedance-measuring contacts, analog filtering to remove EMI, a bridging capacitor to remove DC noise, and digital filtering to further remove EMI, a user's respiration may be measured with the AC-modulation contacts and the impedance-measuring contacts placed at user extremities.

Description

    CROSS-REFERENCE TO RELATED CASES
  • The present application is related to International Application Number PCT/US18/37156, entitled “METHODS AND SYSTEMS FOR PROVIDING A BREATHING RATE CALIBRATED TO A RESONANCE BREATHING FREQUENCY,” filed on Jun. 12, 2018, and to U.S. patent application Ser. No. 16/006,558, entitled “METHODS AND SYSTEMS FOR PROVIDING A BREATHING RATE CALIBRATED TO A RESONANCE BREATHING FREQUENCY,” filed on Jun. 12, 2018 which is a continuation-in-part of U.S. patent application Ser. No. 15/428,115, entitled “STRESS MANAGEMENT USING BIOFEEDBACK,” filed on Feb. 8, 2017, which claims priority to U.S. Provisional Patent Application No. 62/292,450, entitled “WEARABLE APPARATUS WITH BIOFEEDBACK,” filed on Feb. 8, 2016, each of which is hereby incorporated by reference.
  • TECHNICAL FIELD
  • The present disclosure relates to the field of sensors, including, more particularly, to methods and systems for measuring a user's respiration.
  • BACKGROUND
  • It is desirable to be able to measure the respiration rate of a user. For example, heart rate generally increases upon inhalation and decreases upon exhalation, i.e., some heart rate variation is induced by respiration. Heart Rate Variability (HRV) is the variation of the time intervals between heart beats. An increase in HRV is desirable because it is indicative of a heart rate that is variable and responsive to physiological demands. HRV is greatest when individuals breathe at a frequency that is particular to that individual—their resonance breathing frequency (or “resonance breathing rate”). Respiratory Sinus Arrhythmia (RSA) occurs when Heart Rate Variability (HRV) is in synchrony with respiration, shown when variability on an ECG is shortened during inspiration (“inhalation”) and prolonged during expiration (“exhalation”). Thus, it may be desirable to determine a user's respiration rate and whether that rate is in synchrony with HRV.
  • Some existing systems and methods for measuring a user's respiration rate rely on a change in the impedance of the user's chest. That change in impedance is caused by two aspects of a user's respiration: a change in the volume of gas in relation to the surrounding tissue; and a change in the electrical path length across the chest that is caused by the expansion of the chest. The impedance increases as the gas volume and path length increase. To measure that change, electrodes may be placed on the user on either side of the chest and modulation signals (excitation signals of an alternating current signal at a known frequency) may be passed between the electrodes. A base voltage signal is created between the electrodes by the impedance of the user's chest to the AC current when the user has completely exhaled. A respiration voltage signal is imposed on the base voltage signal by the increase in impedance caused by the user's respiration. To determine the respiration voltage signal, the resulting combined voltage signal is demodulated. The respiration frequency is determined from the resulting demodulated voltage signal.
  • FIG. 1 is a prior art circuit diagram for a Texas Instruments ADS1292R from the data sheet for the Texas Instruments ADS1292R, which is a low-power, 2-channel, 24-bit analog-to-digital converter. The datasheet for a Texas Instruments ADS1292R discloses that a feature of the ADS1292R is an integrated respiration impedance measurement. FIG. 1 depicts FIG. 56 from the data sheet for the TI ADS1292R. The pin assignments from the ADS1292R are provided in TABLE 1.
  • TABLE 1
    NAME; TERMINAL; FUNCTION; DESCRIPTION
    AVDD; 12; Supply; Analog supply
    AVSS; 13; Supply; Analog ground
    CLK; 17; Digital input; Master clock input
    CLKSEL; 14; Digital input; Master clock select
    CS; 18; Digital input; Chip select
    DGND; 24; Supply; Digital ground
    DIN; 19; Digital input; SPI data in
    DOUT; 21; Digital output; SPI data out
    DRDY; 22; Digital output; Data ready; active low
    DVDD; 23; Supply; Digital power supply
    GPIO1/RCLK1; 26; Digital input/output; General-purpose I/O 1 or
    resp clock 1 (ADS1292R)
    GPIO2/RCLK2; 25; Digital input/output; General-purpose I/O 2 or
    resp clock 2 (ADS1292R)
    IN1N(1); 3; Analog input; Differential analog negative input 1
    IN1P(1); 4; Analog input; Differential analog positive input 1
    IN2N(1); 5; Analog input; Differential analog negative input 2
    IN2P(1); 6; Analog input; Differential analog positive input 2
    PGA1N; 1; Analog output; PGA1 inverting output
    PGA1P; 2; Analog output; PGA1 noninverting output
    PGA2N; 7; Analog output; PGA2 inverting output
    PGA2P; 8; Analog output; PGA2 noninverting output
    PWDN/RESET; 15; Digital input; Power-down or system reset; active low
    RESP_MODN/IN3N(1); 32; Analog input/output; N-side
    respiration excitation signal for respiration or auxiliary input 3N
    RESP_MODP/IN3P(1); 31; Analog input/output; P-side
    respiration excitation signal for respiration or auxiliary input 3P
    RLDIN/RLDREF; 29; Analog input; Right leg drive input to MUX or
    RLD amplifier noninverting input; connect to AVDD if not used
    RLDINV; 28; Analog input; Right leg drive inverting input;
    connect to AVDD if not used
    RLDOUT; 30; Analog input; Right leg drive output
    SCLK; 20; Digital input; SPI clock
    START; 16; Digital input; Start conversion
    VCAP1; 11; —; Analog bypass capacitor
    VCAP2; 27; —; Analog bypass capacitor
    VREFN; 10; Analog input; Negative reference voltage;
    must be connected to AVSS
    VREFP; 9; Analog input/output; Positive reference voltage
    (1)Connect unused analog inputs to AVDD.
  • According to the data sheet for the TI ADS1292R, the modulation signals are supplied by RESP_MODP and RESP_MODN. Exemplary modulation frequencies are 32 kHz and 64 kHz. Also, according to the data sheet for the TI ADS1292R, if the Right Arm Lead and Left Arm Lead are intended to measure respiration and ECG signals, the two leads are each wired into channel 1 for respiration signals and channel 2 for ECG signals. Accordingly, FIG. 1 depicts the Right Arm Lead wired into IN2N and IN1N and the Left Arm Lead wired into IN1P and IN2P. FIG. 1 further depicts that the Right Arm Lead is also wired into RESP_MODP and that the Left Arm Lead is also wired into RESP_MODP.
  • However, Applicant determined that the result of the circuit disclosed in the data sheet for the TI ADS1292R was unsatisfactory for measuring respiration with the contacts placed at a user's extremities. Thus, there is a need for a system and method for measuring a user's respiration from extremities.
  • BRIEF DESCRIPTION OF THE DRAWINGS
  • The embodiments are illustrated by way of example and not limitation in the figures of the accompanying drawings, in which like references indicate similar elements, and in which:
  • FIG. 1 is a prior art circuit diagram;
  • FIG. 2 is a circuit diagram illustrating aspects of an embodiment of a system for measuring the respiration of a user;
  • FIG. 3 is a circuit diagram further illustrating aspects of the embodiment of a system for measuring the respiration of a user of FIG. 2;
  • FIG. 4 illustrates an embodiment of a method for measuring the respiration of a user;
  • FIG. 5 illustrates an embodiment of a method for measuring the respiration of a user;
  • FIG. 6 illustrates an embodiment of a method for measuring the respiration of a user;
  • FIG. 7 illustrates an embodiment of a method for measuring the respiration of a user;
  • FIG. 8 is a simplified, exemplary block diagram of an embodiment of a system for measuring the respiration of a user;
  • FIG. 9 is an exemplary block diagram of a computing device from the system of FIG. 8;
  • FIG. 10 includes front, back, top, bottom, and right views of an embodiment of a biometric analysis device implementing embodiments of the systems and methods disclosed herein; and
  • FIG. 11 is a perspective view of the biometric analysis device of FIG. 10.
  • DETAILED DESCRIPTION
  • Applicant desired to measure a user's respiration and ECG signals at the user's wrist using a wrist-mounted device. For Applicant, the circuit disclosed in the data sheet for the TI ADS1292R was unsatisfactory for measuring a user's respiration at this extremity because excessive electromagnetic interference (EMI) resulted in noise in the demodulated signal. The noise was large enough to cause errors in the determination of a user's respiration rate. Applicant surmised that the ability of the human body to act as an antenna contributed to the excessive EMI and that attempting to measure respiration from an extremity (i.e., the wrist) further exacerbated the EMI.
  • Embodiments within disclose improved systems and methods for measuring respiration that are suitable for measuring respiration at the user's extremities. The embodiments are discussed using the Texas Instruments ADS1292R processor, but the ADS1292R is an exemplary electronics device and the systems and methods disclosed within may be practiced using other processors, processor sets, circuitry (both digital and analog), or combinations of these. Thus, “processing electronics” may include one or more processors, processor sets, circuitry (both digital and analog), or combinations of these. The improvements may include one or more of the following: 1) providing user-excitation contacts for the AC modulation signals where the user-excitation contacts are separate and distinct from user impedance-measuring contacts; 2) adding a low-pass filter between each user impedance-measuring contact and the respective input into the processing electronics; 3) adding a capacitance between the inputs into the processing electronics; 4) filtering a digital impedance signal within the processing electronics to remove a DC component; 5) filtering the digital impedance signal within the processing electronics with a low-pass filter to remove further noise; and 6) creating long and short running averages of the impedance signal and, from these, determining that the user is inhaling when the short running average is greater than the long running average and that the user is exhaling when the short running average is less than the long running average.
  • FIG. 2 and FIG. 3 are circuit diagrams illustrating aspects of an embodiment of a system for measuring a user's respiration from extremities. FIG. 2 illustrates an embodiment of a modulation circuitry 200, which provides user-excitation contacts for the AC modulation signals that are separate and distinct from user impedance-measuring contacts that are wired into the respiration channel of processing electronics 201. It was determined that providing contacts for the AC-modulation signals that are separate from the impedance-measuring contacts, by itself, significantly reduced noise (e.g., due to EMI) in the impedance measurement. In FIG. 2, modulation circuitry 200 includes a first user-excitation contact (RL) 202 coupled to a respiration modulation excitation signal source 206 from electronics 201 (e.g., a TI ADS1292R) through a capacitance and a resistance 218. In an embodiment the capacitance includes a first capacitor 210 and a second capacitor 214. In FIG. 2, a second user-excitation contact (LL) 204 is coupled to a respiration modulation excitation signal source 208 through a capacitance and a resistance 220. In an embodiment the capacitance includes a first capacitor 212 and a second capacitor 216. In the embodiment of FIG. 2, to provide AC modulation signals that result in an impedance across the user's chest, user- excitation contacts 202 and 204 are placed in contact with the skin of a user and on either side of the user's chest. In an embodiment, a contact may be made, e.g., at each wrist of the user, or at one wrist and a finger of the opposing arm. Exemplary modulation frequencies for the user-excitation signals include 32 kHz and 64 kHz. In an embodiment, resistances 218, 220 may be 40 kΩ, capacitors 210, 212 may be 100 nF, and capacitors 214, 216 may be 2200 pF.
  • FIG. 3 is a circuit diagram further illustrating aspects of the embodiment of a system for measuring a user's respiration from extremities of FIG. 2. FIG. 3 illustrates circuitry 300, which includes circuitry for measuring the impedance of a user at extremities using a first user-extremity contact 302 and a second user-extremity contact 304. In the embodiment of FIG. 3, to measure the impedance that results from the AC modulation signals across the user's chest, user- extremity contacts 302 and 304 are placed in contact with the skin of the user and on either side of the user's chest. In an embodiment, a contact may be made, e.g., at each wrist of the user, or at one wrist and a finger of the opposing arm. FIG. 3 further illustrates that modulation circuitry 200 is completely separate and distinct from the impedance-measuring circuitry between user contacts 302, 304 up to electronics 201. In FIG. 3, for measuring impedance, user-extremity contact 302 is coupled to an impedance-measuring input 310 to electronics 201. In this particular embodiment, input 310 is differential analog negative input 1 to the TI ADS1292R. Second user-extremity contact 304 is coupled to a second input 312 to electronics 201. In this particular embodiment, input 312 is differential analog positive input 1 to the TI ADS1292R. Between contact 302 and input 310 the circuitry further includes a capacitance, voltage biasing circuitry, and a low-pass filter 318. In this particular embodiment, the capacitance includes two capacitors 342, 344. The voltage biasing circuitry includes two resistors 350, 352, each coupled at one end between the capacitance and low-pass filter 318, with resistor 350 coupled to an analog supply voltage 340 and resistor 352 coupled to an analog ground 338. And low-pass filter 318 includes a resistor 330 coupled between the voltage biasing circuitry and input 310 and includes a capacitor 332 coupled between resistor 330 and input 310 at one end and to ground 338 at the other. Between contact 304 and input 312 the circuitry mimics that between contact 302 and input 310, further including a capacitance, voltage biasing circuitry, and a low-pass filter 320. In this particular embodiment, the capacitance includes two capacitors 346, 348. The voltage biasing circuitry includes two resistors 354, 356, each coupled at one end between the capacitance and low-pass filter 320, with resistor 354 coupled to an analog supply voltage 340 and resistor 356 coupled to an analog ground 338. And low-pass filter 320 includes a resistor 334 coupled between the voltage biasing circuitry and input 312 and includes a capacitor 336 coupled between resistor 334 and input 312 at one end and to ground 338 at the other.
  • In the embodiment of FIG. 3, the series capacitance (e.g., capacitors 342, 344 and 346, 348) prevents a potential DC current being applied to the user, with the redundancy of two capacitors protecting against the short-circuiting of one of the capacitors. The voltage-biasing circuitry establishes a pre-determined voltage between the two resistors (e.g., between resistors 350 and 352 and between resistors 354 and 356) that, in this embodiment, is half-way between analog ground 338 and analog supply voltage 340. Low-pass filters (e.g., low-pass filter 318 and 320) reduce EMI significantly, which contributes to the ability of the embodiment to measure a user's respiration when user- contacts 302, 304 are placed on the user's extremities. Embodiments may further include a capacitance between the impedance-sensing inputs to the electronics that is sized to reduce DC noise. In FIG. 3, such a capacitance is represented by a capacitor 358 coupled between inputs 310 and 312.
  • In an embodiment, the elements of circuit 300 may have the following values: capacitors 342, 346 may be 100 nF; capacitors 344, 348 may be 2200 pF; resistors 350, 352, 354, 356 may be 10 MΩ; resistors 330, 334 may be 220 kΩ; capacitors 332, 336 may be 22 pF; and capacitor 358 may be 10 pF.
  • Thus, in the specific embodiment of FIG. 3, low- pass filters 318, 320 have cut-off frequencies 32.9 kHz. In other embodiments, low- pass filters 318, 320 may have other cut-off frequencies and still reduce EMI sufficiently to allow measuring a user's respiration at extremities. In general, the cut-off frequencies of low- pass filters 318, 320 are chosen to narrow the band that must be filtered later by digital filters within electronics 201. By narrowing the band, digital filters with better response may be chosen. In an embodiment, the cut-off frequencies may be between thirty and thirty-five kilohertz. Thus, in an embodiment, low- pass filters 318, 320 work in combination with signal-processing logic within electronics 201 to even further reduce EMI because low- pass filters 318, 320 may have cut-off frequencies determined to work synergistically with signal-processing logic within electronics 201. In an embodiment, low- pass filters 318, 320 have cut-off frequencies chosen to reduce relatively high-frequency EMI, e.g., EMI frequencies of from 100 kHz to 1000 kHz, and the digital filtering discussed within is directed to filtering out substantially lower frequencies, e.g., with cutoff frequencies of from 0.4 Hz to 20 Hz. The hardware low- pass filters 318, 320 filter out most of the noise that comes from the user's body to the circuit and the digital filters within electronics 201 may then be optimized (e.g., with filters that have improved response times) to address board noise of substantially lower frequencies, primarily 24 Hz and 60 Hz. The two different low pass filtering systems work together to provide a usable respiration signal. Further smoothing of that signal is applied digitally as discussed within, e.g., regarding FIGS. 4-7.
  • FIG. 3 further illustrates an embodiment of a system for measuring a user's ECG at extremities. For reasons that are similar to those when measuring respiration at extremities, measuring a user's ECG at extremities suffers from increased EMI. In FIG. 3, circuitry 300 illustrates an embodiment of ECG-measuring circuitry for measuring the impedance of a user at extremities using first user-extremity contact 302 and second user-extremity contact 304 when user contacts 302, 304 are placed in contact with the skin of the user and on either side of the user's chest, e.g., at each wrist of the user, or at one wrist and a finger of the opposing arm. In FIG. 3, for measuring a user's ECG, a low-pass filter 314 is coupled between user-extremity contact 302 and an input 306 to electronics 201. In this particular embodiment, input 306 is differential analog negative input 2 to the TI ADS1292R chip. Low-pass filter 314 includes a resistor 322 coupled between user contact 302 and input 306 and includes a capacitor 324 coupled between resistor 322 and input 306 at one end and to ground 338 at the other. Between contact 304 and input 308 the circuitry mimics that between contact 302 and input 306, with low-pass filter 316 including a resistor 326 coupled between user contact 304 and input 308 and includes a capacitor 328 coupled between resistor 326 and input 308 at one end and to ground 338 at the other. In an embodiment, low- pass filters 314, 316 have cutoff frequencies that are chosen for anti-aliasing the signals to inputs 306, 308, which means their cutoff frequencies are substantially higher than those of low- pass filters 318, 320. For example, in an embodiment, the cutoff frequencies of low- pass filters 314, 316 may be 60,000 Hz.
  • In the embodiment of FIG. 2 and FIG. 3, electronics 201 includes instructions, which, when contacts 202, 204, 302, 304 are in contact with a user, cause electronics 201 to determine the impedance between user extremity contacts 302 and 304 and measure the user's respiration rate. The instructions are further discussed regarding FIGS. 4-7.
  • In an embodiment, electronics 201 may include a first processor and a second processor. In the embodiment, the first processor includes electronics contacts 206, 208, 310, 312. The first processor creates a digital impedance signal corresponding to analog impedance data from user contacts 302, 304 and provides the digital impedance signal to the second processor for subsequent digital signal processing. In an embodiment, the first processor may be a TI ADS1292R analog-to-digital converter and the second processor may be an Arm Cortex M4.
  • FIG. 4 illustrates an embodiment of a method 400 for measuring a user's respiration from an extremity of the user. In the embodiment, method 400 is performed with first and second user contacts on opposing sides of the user's chest and the third and fourth user contacts also on opposing sides of the user's chest. In method 400, at step 410, an AC current is provided between first and second user contacts, causing an impedance to develop between third and the fourth user contacts. In an embodiment, the contacts may be at a user's extremity, e.g., a user's wrist, or a user's finger. In step 412, the impedance is detected between the third and the fourth user contacts, the impedance changing with time due to the respiration of the user. In step 414, based on the detected change of the impedance with time, a signal is created that may be used to indicate the respiration rate of the user. The signal is created, in part, by demodulating the detected impedance to separate the contribution from the user's respiration from the contribution from the AC modulation signal. In step 416, at least one step from the following steps may be performed: the signal is stored in memory; the signal is displayed with an electronic device, and the signal is provided to a processor for further processing.
  • It was determined that the impedance measurement of method 400 is improved (i.e., has less noise) when performed using the embodiments of the system described regarding FIG. 2 and FIG. 3. Thus, in an embodiment, steps 410-416 may be performed using an embodiment of a system described in FIG. 2 and FIG. 3, with the embodiment providing a signal indicating a respiration rate of the user and benefitting from noise-reduction contributions provided by embodiments of the system described regarding FIG. 2 and FIG. 3.
  • FIG. 4 indicates additional steps, one or more of which may be added between steps 412 and 414 to assist in creating the signal that may be used to indicate the respiration rate of the user. In step 418, an impedance signal may be created from the impedance detected in step 412 between the third and the fourth user contacts. In step 420, the impedance signal may be filtered to remove a DC component, which was determined to exist even after demodulation. In an embodiment, the filtering to remove a DC component may use a digital filter. In an embodiment, the digital filter may be an infinite impulse response (IIR) filter for DC current with a filtering constant of 0.992. In step 422, the impedance signal may be filtered through a low-pass filter, e.g., to further remove EMI. In an embodiment, the low-pass filter may be a digital filter. In an embodiment, the digital low-pass filter may be a finite impulse response (FIR) low-pass filter. In an embodiment, the filter is chosen to permit frequencies associated with breathing rates, including the particularly desired (or “targeted”) breathing rates. In an embodiment, the FIR may be a 179th order filter with a gain of 1 with 5 dB from 0 to 0.5 Hz and a gain of 0 from 3 Hz and above and with −40 dB attenuation. In an embodiment, the FIR may be a 179th order filter with a gain of 1 with 5 dB from 0 to 2 Hz and a gain of 0 from 3 Hz and above and with −40 dB attenuation. In an embodiment, the impedance signal may be filtered by a band-pass filter. In an embodiment, the band-pass filter may be a digital filter. In an embodiment, the digital band-pass filter may be a combination of the IIR filter for DC current and the FIR low-pass filter.
  • It was determined that steps 420, 422 are effective in reducing noise in the impedance measurement, both individually and in combination. Thus, in embodiments, one or both of steps 420, 422 may be performed with steps 410-416 to provide a signal indicating a respiration rate of the user and benefitting from noise-reduction contribution from each added step.
  • It was also determined that the benefits in reduced noise provided by steps 420, 422 were additive to the improvements provided using the embodiments of the system described regarding FIG. 2 and FIG. 3. Thus, in an embodiment, steps 410-416 may be performed using an embodiment of a system described in FIG. 2 and FIG. 3, with the embodiment of method and system providing a signal indicating a respiration rate of the user and benefitting from the noise-reduction contributions of step 420 or step 422 or both.
  • FIG. 5 illustrates an embodiment of a method 500 for measuring a user's respiration from extremities. In FIG. 500 describes steps that may be performed on an impedance signal created from the detected impedance between the third and fourth user contacts (as in any of the signals created in steps 412, 418, 420, or 422, before they are provided to step 414) from which a signal indicting a respiration rate of the user is created as in step 414. In step 502, from an impedance signal created from the time-varying impedance detected between the third and fourth user contacts, a first running average is created over a first running period of time. In step 504, from the same impedance signal of step 502, a second running average is created from a second running period of time, where the second running period of time is substantially shorter than the first running period of time. In step 506, the first and second running averages are compared and if the second running average is greater than the first, it is determined that the user is inhaling. Conversely, in step 508, if the second running average is less that the first, it is determined that the user is exhaling. In step 510, the durations of time between the determinations of when the user is inhaling and exhaling are used to create the signal indicating the respiration rate of the user.
  • In the embodiment of FIG. 5, the longer running average is taken over a period of time with a duration sufficient to determine the average impedance of at least one entire wave, i.e., an entire respiration cycle. This effectively provides the center amplitude of the wave (or the “baseline”). Thus, taking the longer running average is a form of a DC component filtering over and above the IIR filter mentioned earlier. In the embodiment, the shorter running average is taken over a period of time with a duration that reduces noise without filtering out the impedance change caused by the user's respiration. In an embodiment, the shorter running average is taken over a 2-second window and the longer running average is taken over an 11-second window. The shorter running average is also a form of filtering that is over and above the FIR filter mentioned earlier.
  • In embodiments, the methods discussed regarding FIG. 4, or FIG. 5, or both, may be performed by embodiments of systems discussed regarding FIG. 2 and FIG. 3. In embodiments, the methods of FIG. 4 and FIG. 5 may be performed by electronics 201 where electronics 201 includes a first processor and a second processor. In these embodiments, the first processor includes electronics contacts 206, 208, 310, 312. The first processor creates a digital impedance signal corresponding to analog impedance data from user contacts 302, 304 and provides the digital impedance signal to the second processor for subsequent digital signal processing. In an embodiment, the first processor may be a TI ADS1292R analog-to-digital converter and the second processor may be an Arm Cortex M4.
  • In an embodiment, the filtering power of low- pass filters 318, 320 is increased (or the filtering is “front loaded”), which allows the digital filtering described regarding FIG. 4 and FIG. 5 to be fine-tuned and directed to the remaining noise, thus enhancing the overall noise-reducing effect of the embodiment over changes to just the circuits 200, 300 or to just the methods 400, 500.
  • FIG. 6 illustrates an embodiment of a method 600 for measuring the respiration of a user. The embodiment of FIG. 6 is directed to processing that may be performed on a digital signal created from the changes in impedance caused by a user's respiration, e.g., a digital signal created from the impedance from step 412 of method 400, or a digital impedance signal created by electronics 201 and further processed by software within electronics 201. In FIG. 6, in step 602, a data point indicative of an impedance is received (or taken) at a pre-determined frequency, e.g., every 2 ms (i.e., the sampling rate is 500 Hz). In step 604, a pre-determined number of data points are summed, e.g., 10 data points may be summed. In step 606, after the data points are summed, a filter is implemented that produces a filtered data point at a predetermined frequency, e.g., every 20 ms (i.e., 50 Hz). In step 608, a single-order IIR filtering is performed on the data from step 606 to reduce DC noise. In an embodiment, this IIR filter is an IIR filter from Texas Instruments included with the TI ADS1292R digital-to-analog converter. In step, 610, the data stream from step 608 is further filtered using a low-pass FIR filter, e.g., a 179th-order low-pass FIR filter with a cut-off frequency of 0.4 Hz. With the data being sampled at a sufficiently high frequency, e.g., 50 Hz, an FIR filter may be employed with such a low cut-off frequency without the number of taps being too large for the processor to accommodate (i.e., a lower-order FIR filter). In step 612, a running average, e.g., a 10-sample running average, is used to smooth the output from the FIR filter and prepare the data for a differentiation filter. In step 614, the data is filtered with a differentiation filter, e.g., a 5th-order differentiation filter, which removes high-frequency components from the data. If the output of step 614 is larger than 0, then the user is determined to be inhaling. Otherwise the user is exhaling. In step 616, the data is integrated using a moving window integrator with, e.g., a 50-sample window, which at this sampling rate is 1 second of data. The output of step 616 may be used to compare the phase angle of the user's respiration with a target respiration. In an embodiment, the user's respiration rate may be determined using the time between zero-transitions with the data from step 614. In an embodiment, the determined user respiration rate may be compared to the changes in the user's HRV to determine whether the user's HRV is in synchrony with the user's respiration (i.e., whether the user is in RSA). In an embodiment, the signal from step 412 may be processed as described in steps 608-614 with the resulting signal supplied to step 414. In an embodiment, the signal from step 412 may be processed as described in steps 602-614 with the resulting signal supplied to step 414.
  • FIG. 7 illustrates an embodiment of a method 700 for measuring the respiration of a user that corrects for (or “cancels out”) skewing that might be induced due the user's skin varying in a level of moistness while respiration is being measured. Method 700 builds on method 600. In step 702, the zeroes in the differentiation-filtered output of step 614 are used to find the local minimums and maximums of the user's respiration. In step 704, a running average is created from the local minimums and a running average is created from the local maximums. In step 706, the output of step 614 is rescaled by dividing positive values by the running average of the local maximums and by dividing negative values by the running average of the local minimums. The result of step 706 is that the respiration data will be a scaled wave that ranges from −1 to 1, where positive values indicate the user is inhaling and negative values indicate the user is exhaling. With the respiration data being maintained between −1 and 1, the skew is eliminated. In an embodiment, the running average of step 704 is constructed using the last ten (10) local minimums and last ten (10) local maximums.
  • FIG. 8 is a simplified, exemplary block diagram of an embodiment of a system 800 for implementing the embodiments of systems and methods disclosed herein. System 800 may include a number of sensors, e.g., a respiration rate sensor 805 (e.g., as described within this disclosure) and a heart rate sensor 810 (e.g., as described within this disclosure), for developing data regarding a user. Sensors 805, 810, and 820 are in communication with a computing device 815. Computing device 815 may further be in control of a haptic device 825 and a buzzer or speaker (not shown) for communicating with the user. System 800 may be referred to as a Biometric Analysis Device.
  • Respiration rate sensor 805 may be an impedance-based sensor as discussed within this specification. Heart rate sensor 810 may be, e.g., a plurality of sensors sufficient to produce an electrocardiogram (ECG, as discussed within), a chest-mounted device, or a wrist-mounted device, so long as the device provides heart rate data with sufficient accuracy and precision. Sensor 820 is representative of additional sensors that may be included, such as sensors for determining galvanic skin response, temperature, blood pressure, hydration, sleep, exercise activity, brain activity, nutrient levels, or blood analysis. Sensors 805, 810, and 820 may supply data to computing device 815 via communication links 830.
  • Computing device 815 may include a user interface and software, which may implement the steps of the methods disclosed within. Computing device 815 may receive data from sensors 805, 810, and 820, via communication links 830, which may be hardwire links, optical links, satellite or other wireless communications links, wave propagation links, or any other mechanisms for communication of information. Various communication protocols may be used to facilitate communication between the various components shown in FIG. 8. Distributed system 800 in FIG. 8 is merely illustrative of an embodiment and does not limit the scope of the systems and methods as recited in the claims. In an embodiment, the elements of system 800 are incorporated into a single, wearable Biometric Analysis Device (e.g., as described regarding FIGS. 10 and 11). One of ordinary skill in the art would recognize other variations, modifications, and alternatives. For example, more than one computing device 815 may be employed. As another example, sensors 805, 810, and 820 may be coupled to computing device 815 via a communication network (not shown) or via some other server system.
  • Computing device 815 may be responsible for receiving data from sensors 805, 810, and 820, performing processing required to implement the steps of the methods, and for interfacing with the user. In some embodiments, computing device 815 may receive processed data from sensors 805, 810, and 820. In some embodiments, the processing required is performed by computing device 815. In such embodiments, computing device 815 runs an application for receiving user data, performing the steps of the method, and interacting with the user. In other embodiments, computing device 815 may be in communication with a server, which performs the required processing, with computing device 815 being an intermediary in communications between the user and the processing server.
  • System 800 enables users to access and query information developed by the disclosed methods. Some example computing devices 815 include desktop computers, portable electronic devices (e.g., mobile communication devices, smartphones, tablet computers, laptops) such as the Samsung Galaxy Tab®, Google Nexus devices, Amazon Kindle®, Kindle Fire®, Apple iPhone®, the Apple iPad®, Microsoft Surface®, the Palm Pre™, or any device running the Apple iOS®, Android® OS, Google Chrome® OS, Symbian OS®, Windows Mobile® OS, Windows Phone, BlackBerry® OS, Embedded Linux, Tizen, Sailfish, webOS, Palm OS® or Palm Web OS®; or wearable devices such as smart watches, smart fitness or medical bands, and smart glasses.
  • FIG. 9 is an exemplary block diagram of a computing device 815 from the system of FIG. 8. In an embodiment, a user interfaces with the system through computing device 815, which also receives data and performs the computational steps of the embodiments. Computing device 815 may include a display, screen, or monitor 905, housing 910, input device 915, sensors 950, and a security application 945. Housing 910 houses familiar computer components, some of which are not shown, such as a processor 920, memory 925, battery 930, speaker, transceiver, antenna 935, microphone, ports, jacks, connectors, camera, input/output (I/O) controller, display adapter, network interface, mass storage devices 940, and the like. In an embodiment, sensors 950 may include sensors 805, 810, and 820 incorporated into computing device 815, and haptic device 825 may also be incorporated into device 815. In an embodiment, housing 910 is the housing of the wearable biometric analysis device 1000 of FIGS. 10 and 11.
  • Input device 915 may also include a touchscreen (e.g., resistive, surface acoustic wave, capacitive sensing, infrared, optical imaging, dispersive signal, or acoustic pulse recognition), keyboard (e.g., electronic keyboard or physical keyboard), buttons, switches, stylus, or combinations of these.
  • Display 904 may include dedicated LEDs for providing directing signals and feedback to a user.
  • Mass storage devices 940 may include flash and other nonvolatile solid-state storage or solid-state drive (SSD), such as a flash drive, flash memory, or USB flash drive. Other examples of mass storage include mass disk drives, floppy disks, magnetic disks, optical disks, magneto-optical disks, fixed disks, hard disks, CD-ROMs, recordable CDs, DVDs, recordable DVDs (e.g., DVD-R, DVD+R, DVD-RW, DVD+RW, HD-DVD, or Blu-ray Disc), battery-backed-up volatile memory, tape storage, reader, and other similar media, and combinations of these.
  • System 900 may also be used with computer systems having configurations that are different from computing device 815, e.g., with additional or fewer subsystems. For example, a computer system could include more than one processor (i.e., a multiprocessor system, which may permit parallel processing of information) or a system may include a cache memory. The computing device 815 shown in FIG. 9 is but an example of a computer system suitable for use. For example, in a specific implementation, computing device 815 is a wrist-mounted Biometric Analysis Device in communication with or incorporating the sensors of FIG. 9. An example of such a Biometric Analysis Device is discussed regarding device 1000 of FIGS. 10 and 11. Other configurations of subsystems suitable for use will be readily apparent to one of ordinary skill in the art. In other specific implementations, computing device 815 is a mobile communication device such as a smartphone or tablet computer. Some specific examples of smartphones include the Droid Incredible and Google Nexus One®, provided by HTC Corporation, the iPhone® or iPad®, both provided by Apple, BlackBerry Z10 provided by BlackBerry (formerly Research In Motion), and many others. The Biometric Analysis Device may be a laptop or a netbook. In another specific implementation, the Biometric Analysis Device is a non-portable computing device such as a desktop computer or workstation.
  • In an embodiment, system 900 may be incorporated into a single module. The module may have four user contacts (or “electrodes”) placed to allow a user to make contact with two contacts with one user extremity and with the other two contacts with the other user extremity. This module can be contained within numerous types of wristband straps (leather, etc.) and form factors (such as key chain, steering wheel cover, etc.). The module, or the strap or other form factor, may also include a small OLED display to display the current time. The module may execute software that performs an embodiment of the method. Accordingly, the module may provide the user with feedback, e.g., an indication of the user's respiration rate or heart rate or both.
  • FIG. 10 includes front, back, top, bottom, and right views of an embodiment of a wearable biometric analysis device 1000 for implementing embodiments of the methods disclosed within. Components and capabilities of biometric analysis device 1000 are also described with reference to FIGS. 2-9. Biometric Analysis Device 1000 includes a computing device 1005 and a sensor coupled to electrical contacts 1010, 1012, 1014, 1016 that acquire data that may be used to provide a measure of the user's respiration rate as discussed above. Computing device 1005 processes biometric data measured by the sensor(s) and produces feedback correlating to the processed biometric data. By continuously monitoring one or more biometric values, the user may respond to the data received and modify their behavior or activity to improve health and performance. The biometric analysis device 1000 thereby provides feedback by sensing and reporting a biometric value measured by the sensor to the user in real time. In an embodiment, contacts 1010, 1012, 1014, 1016 provide data to a TI ADS1292R sensor. As such, Biometric Analysis Device 1000 may be equipped with both a respiration rate sensor and a heart rate sensor. Computing device 1005 is in communication with the sensor or sensors associated with contacts 1010, 1012, 1014, 1016. Computing device 1005 may also control a haptic device (not shown) for communicating with the user. Computing device 1005 may include a display 1015, a user interface, and software, for implementing the steps of the methods disclosed within. In an embodiment, contacts 1010 and 1012 may correspond to contacts 202 and 302 as described above, and contacts 1014 and 1016 may correspond to contacts 204 and 304 as described above. In the embodiment, a method for determining the user's respiration rate includes the user placing device 1000 on one of the user's wrists such that contacts 1010, 1012 are in contact with the user's wrist. Then, the user brings contacts 1014, 1016 in contact with another part of the user's body such as one or more fingers on the user's opposing hand. In other words, the user touches contacts 1014, 1016 to a part of the user's body so that some or all of the user's chest is between contact pairs 1010, 1012 and 1014, 1016 (the circuits are described with reference to FIGS. 2 and 3 and contact pairs 202, 302 and 204, 304). In an embodiment, the part of the user's body may be a finger or other part of the opposing arm, may be a section of the user's torso, or may be a section of a leg of the user. With both contact pairs 1010, 1012 and 1014, 1016 in such contact with the user, the device then determines the user's respiration rate, heart rate, or both according to the methods described within.
  • Computing device 1005 may receive data from sensors 1010, 1012, 1014, 1016, perform processing required to implement the steps of the methods disclosed within, and provide a user interface via display 1015. In some embodiments, all processing required is performed by computing device 1005. In such embodiments, computing device 1005 executes instructions for receiving user data, performing the steps of the method, and interacting with the user. In other embodiments, computing device 1005 may be in communication with a server, which performs part of the required processing, with computing device 1005 being an intermediary in communications between the user and the processing server.
  • As illustrated, Biometric Analysis Device 1000 generally comprises a band 1020 configured to be worn about a wrist of the user. The band 1020 includes an adjustment mechanism 1025, for adjusting a circumference of the band 1020. A user can thus select, using adjustment mechanism 1025, a particular size for positioning band 1020 about the user's wrist. A visual indication, e.g., for feedback, may be provided by display 1015. In an embodiment, visual indicators may be further be positioned on the band 1020 to provide visual signals to the user. Sensor(s) associated with contacts 1010, 1012, 1014, 1016 may be configured to be activated by computing device 1005. In an embodiment, additional sensors, e.g., a temperature sensor or a galvanic response sensor, may be provided to provide more user data for determining vagal tone. In an embodiment, one or more translucent windows may be positioned about the band 1020 to transmit light from one or more indicators positioned with the band 1020.
  • Biometric analysis device 1000, in one embodiment, is used measure a user's respiration rate. Accordingly, the biometric analysis device 1000 may provide the user with real-time, personal biofeedback. In an embodiment, device 1000 may measure both a user's respiration rate and heart rate and provide feedback regarding one or both. The biofeedback may allow the user to learn about the user's personal physiological state and physiological responses. As a result, the biofeedback provided to the user (by, e.g., one or more of display 1015, or haptic device, or speaker) may enable the user to self-regulate the user's activity and behavior to improve the user's performance or health. In an embodiment, device 1000 may provide a user with feedback (e.g., a vibration pattern of frequency, duration, and magnitude) selected to encourage a desired behavior. In an embodiment, biometric analysis device 1000 is configured to provide the user with feedback with reference to previously-collected biometric data, such as respiration rate or heart rate variability. The biometric analysis device 1000 may emit vibrations based on the user's actual respiration rate, or a target respiration rate. For example, a visual indication from, e.g., display 1015, may be provided and configured to emit different colors based on when the user is supposed to inhale and exhale for deep breathing relaxation techniques. The user may also be capable of changing the breathing intervals. The visual indication and breathing intervals may be enabled and adjusted through the user interface.
  • FIG. 11 is a perspective view of the biometric analysis device of FIG. 10.
  • FIGS. 10 and 11 illustrate one example embodiment of a wearable biometric analysis device 1000 that is configured to measure the respiration rate of a user. In one embodiment, biometric analysis device 1000 can include each of the elements of system 800 of FIG. 8 and FIG. 9. In other embodiments, biometric analysis device 1000 can include other elements that function with biometric analysis device 1000 to provide biometric measurement and analysis to assist a user with stress management.
  • In the description above and throughout, numerous specific details are set forth in order to provide a thorough understanding of an embodiment of this disclosure. It will be evident, however, to one of ordinary skill in the art, that an embodiment may be practiced without these specific details. In other instances, well-known structures and devices are shown in block diagram form to facilitate explanation. The description of the preferred embodiments is not intended to limit the scope of the claims appended hereto. Further, in the methods disclosed herein, various steps are disclosed illustrating some of the functions of an embodiment. These steps are merely examples and are not meant to be limiting in any way. Other steps and functions may be contemplated without departing from this disclosure or the scope of an embodiment.

Claims (17)

1.-10. (canceled)
11. A wrist-mountable device including:
electronics including a processor with memory and instructions;
a first user contact disposed on a first side of the device;
a second user contact disposed on a second side of the device;
a third user contact disposed on the first side of the device; and
a fourth user contact disposed on the second side of the device or a third side of the device,
wherein:
when the device is mounted on the user, and the first side of the device is positioned against a first arm of the user, the first user contact and the third user contact make contact with the first arm of the user and are not accessible by a second arm of the user, and the second user contact and fourth user contact are accessible by the second arm; and
the instructions, when executed by the processor with the first and third user contacts in contact with the first arm and the second and fourth user contacts in contact with the second arm, cause the electronics to:
provide an AC current between the first and second user contacts, the AC current causing an impedance to develop between the third and the fourth user contacts;
detect the impedance between the third and the fourth user contacts, the impedance changing with time; and
based on the detected change of the impedance with time, create a signal indicating a respiration rate of the user.
12. The device of claim 11, wherein the instructions further cause the electronics to:
create an impedance signal from the detected impedance between the third and the fourth user contacts;
filter the impedance signal to remove a DC component; and
filter the impedance signal through a low-pass filter.
13. The device of claim 12, wherein the low-pass filter has a cut-off frequency of two hertz and the attenuation is minus forty decibels per decade above three hertz.
14.-19. (canceled)
20. The device of claim 11, wherein the electronics includes a Texas Instruments ADS1292R analog-to-digital converter and an Arm Cortex M4 processor and first through fourth electronics contacts are on the Texas Instruments ADS1292R analog-to-digital converter.
21. A method comprising:
providing a user with a wrist-mountable device including:
electronics including a processor with memory and instructions;
a first user contact disposed on a first side of the device;
a second user contact disposed on a second side of the device;
a third user contact disposed on the first side of the device; and
a fourth user contact disposed on the second side of the device or a third side of the device,
wherein:
when the device is mounted on the user, and the first side of the device is positioned against a first arm of the user, the first user contact and the third user contact make contact with the first arm of the user and are not accessible by a second arm of the user, and the second user contact and fourth user contact are accessible by the second arm;
bringing the first and third user contacts in contact with the first arm and the second and fourth user contacts in contact with the second arm:
providing, by the wrist-mountable device, an AC current between the first and second user contacts, the AC current causing an impedance to develop between the third and the fourth user contacts;
detecting, by the wrist-mountable device, the impedance between the third and the fourth user contacts, the impedance changing with time; and
based on the detected change of the impedance with time, creating, by the wrist-mountable device, a signal indicating a respiration rate of the user.
22. The method of claim 21, further including:
creating, by the wrist-mountable device, an impedance signal from the detected impedance between the third and the fourth user contacts;
filtering, by the wrist-mountable device, the impedance signal to remove a DC component; and
filtering, by the wrist-mountable device, the impedance signal through a low-pass filter.
23. The method of claim 22, wherein the low-pass filter has a cut-off frequency of two hertz and the attenuation is minus forty decibels per decade above three hertz.
24. The method of claim 21, wherein the electronics includes a Texas Instruments ADS1292R analog-to-digital converter and an Arm Cortex M4 processor and first through fourth electronics contacts are on the Texas Instruments ADS1292R analog-to-digital converter.
25. A non-transitory computer-readable medium encoded with a plurality of instructions which, when executed by a processor of a wrist-mounted device including:
electronics including the processor and memory;
a first user contact disposed on a first side of the device;
a second user contact disposed on a second side of the device;
a third user contact disposed on the first side of the device; and
a fourth user contact disposed on the second side of the device or a third side of the device, wherein:
when the device is mounted on the user, and the first side of the device is positioned against a first arm of the user, the first user contact and the third user contact make contact with the first arm of the user and are not accessible by a second arm of the user, and the second user contact and fourth user contact are accessible by the second arm; and
with the first and third user contacts in contact with the first arm and the second and fourth user contacts in contact with the second arm, cause the wrist-mounted device to:
provide an AC current between the first and second user contacts, the AC current causing an impedance to develop between the third and the fourth user contacts;
detect the impedance between the third and the fourth user contacts, the impedance changing with time; and
based on the detected change of the impedance with time, create a signal indicating a respiration rate of the user.
26. The computer-readable medium of claim 25, the instructions further causing the wrist-mounted device to:
create an impedance signal from the detected impedance between the third and the fourth user contacts;
filter the impedance signal to remove a DC component; and
filter the impedance signal through a low-pass filter.
27. The computer-readable medium of claim 26, wherein the low-pass filter has a cut-off frequency of two hertz and the attenuation is minus forty decibels per decade above three hertz.
28. The computer-readable medium of claim 25, wherein the electronics includes a Texas Instruments ADS1292R analog-to-digital converter and an Arm Cortex M4 processor and first through fourth electronics contacts are on the Texas Instruments ADS1292R analog-to-digital converter.
29. The device of claim 11, wherein the second user contact and fourth user contact being accessible by the second arm includes the second user contact and fourth user contact being accessible by one or more fingers on a hand of the second arm.
30. The method of claim 21, wherein the second user contact and fourth user contact being accessible by the second arm includes the second user contact and fourth user contact being accessible by one or more fingers on a hand of the second arm.
31. The computer-readable medium of claim 25, wherein the second user contact and fourth user contact being accessible by the second arm includes the second user contact and fourth user contact being accessible by one or more fingers on a hand of the second arm.
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Family Cites Families (68)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5682898A (en) 1995-04-19 1997-11-04 Colin Corporation Respiration rate measuring apparatus
US5722997A (en) * 1996-09-17 1998-03-03 Sulzer Intermedics Inc. Method and apparatus for cardiac impedance sensing
AUPP711998A0 (en) 1998-11-13 1998-12-10 Micromedical Industries Limited Wrist mountable monitor
US6305943B1 (en) 1999-01-29 2001-10-23 Biomed Usa, Inc. Respiratory sinus arrhythmia training system
US6212427B1 (en) 1999-02-02 2001-04-03 J&J Engineering Heart rate variability feedback monitor system
US6358201B1 (en) 1999-03-02 2002-03-19 Doc L. Childre Method and apparatus for facilitating physiological coherence and autonomic balance
US8764673B2 (en) 1999-03-02 2014-07-01 Quantum Intech, Inc. System and method for facilitating group coherence
US7163512B1 (en) 2000-03-01 2007-01-16 Quantum Intech, Inc. Method and apparatus for facilitating physiological coherence and autonomic balance
US8123696B2 (en) 1999-03-02 2012-02-28 Quantum Intech, Inc. Physiological coherence in animals
US8543197B2 (en) 1999-03-02 2013-09-24 Quantum Intech, Inc. Portable device and method for measuring heart rate
US6377845B1 (en) 2000-07-25 2002-04-23 Datascope Investment Corp. Method and device for sensing impedance respiration
JP2002112969A (en) 2000-09-02 2002-04-16 Samsung Electronics Co Ltd Device and method for recognizing physical and emotional conditions
US6836681B2 (en) 2001-02-15 2004-12-28 Jon R. Stabler Method of reducing stress
WO2003079891A2 (en) 2002-03-18 2003-10-02 Sonomedica, Llc Method and system for generating a likelihood of cardiovascular disease from analyzing cardiovascular sound signals.
US7200440B2 (en) 2003-07-02 2007-04-03 Cardiac Pacemakers, Inc. Cardiac cycle synchronized sampling of impedance signal
JP2007501657A (en) 2003-08-08 2007-02-01 クアンタム・インテック・インコーポレーテッド Electrophysiological intuition indicator
EP1680010A4 (en) 2003-11-04 2009-07-01 Quantum Intech Inc Systems and methods for facilitating physiological coherence using respiration training
US20050209504A1 (en) 2004-03-18 2005-09-22 Elliott Stephen B Method of presenting audible and visual cues for synchronizing the breathing cycle with an external timing reference for purposes of synchronizing the heart rate variability cycle with the breathing cycle
CN1968727B (en) 2004-03-18 2010-12-22 里普朗尼克股份有限公司 Methods and devices for relieving stress
US8002711B2 (en) 2005-03-18 2011-08-23 Respironics, Inc. Methods and devices for relieving stress
US7618378B2 (en) 2005-06-13 2009-11-17 The University Of Vermont And State Agricultural College Breath biofeedback system and method
USD554266S1 (en) 2006-06-13 2007-10-30 Quantum Intech, Inc. Portable device for measuring heart rate
US7556038B2 (en) 2006-08-11 2009-07-07 Ric Investments, Llc Systems and methods for controlling breathing rate
US8523758B1 (en) 2007-05-02 2013-09-03 Ric Investments, Llc System and method of treatment for insomnia and occasional sleeplessness
US8630704B2 (en) 2007-06-25 2014-01-14 Cardiac Pacemakers, Inc. Neural stimulation with respiratory rhythm management
EP2100556A1 (en) 2008-03-14 2009-09-16 Koninklijke Philips Electronics N.V. Modifying a psychophysiological state of a subject
US8936556B2 (en) 2008-09-24 2015-01-20 Cardiac Pacemakers, Inc. Minute ventilation-based disordered breathing detection
US8666482B2 (en) 2009-01-08 2014-03-04 Simon Christopher Wegerif Method, system and software product for the measurement of heart rate variability
US8396537B2 (en) * 2009-04-20 2013-03-12 Mindray Ds Usa, Inc. Method and system to measure ECG and respiration
US8509882B2 (en) 2010-06-08 2013-08-13 Alivecor, Inc. Heart monitoring system usable with a smartphone or computer
US9351654B2 (en) 2010-06-08 2016-05-31 Alivecor, Inc. Two electrode apparatus and methods for twelve lead ECG
US8301232B2 (en) 2010-06-08 2012-10-30 Alivecor, Inc. Wireless, ultrasonic personal health monitoring system
US20110301439A1 (en) 2010-06-08 2011-12-08 AliveUSA LLC Wireless, ultrasonic personal health monitoring system
US9113807B2 (en) 2010-12-29 2015-08-25 St. Jude Medical, Atrial Fibrillation Division, Inc. Dynamic adaptive respiration compensation with automatic gain control
JP5650575B2 (en) 2011-03-30 2015-01-07 ユニ・チャーム株式会社 Absorbent articles for pets
US20150073285A1 (en) 2011-05-16 2015-03-12 Alivecor, Inc. Universal ecg electrode module for smartphone
US20140050321A1 (en) 2012-08-16 2014-02-20 David E. Albert Ultrasonic transmission of signals
US20130197320A1 (en) 2012-01-26 2013-08-01 David E. Albert Ultrasonic digital communication of biological parameters
WO2014036436A1 (en) 2012-08-30 2014-03-06 Alivecor, Inc. Cardiac performance monitoring system for use with mobile communications devices
WO2014074913A1 (en) 2012-11-08 2014-05-15 Alivecor, Inc. Electrocardiogram signal detection
US9830832B2 (en) 2012-12-20 2017-11-28 Halare, Inc. Automated systems, methods, and apparatus for breath training
US9332941B2 (en) 2012-12-31 2016-05-10 Tosense, Inc. Body-worn sensor for characterizing patients with heart failure
US9974444B2 (en) * 2012-12-31 2018-05-22 Tosense, Inc. Body-worn sensor for characterizing patients with heart failure
WO2014107700A1 (en) 2013-01-07 2014-07-10 Alivecor, Inc. Methods and systems for electrode placement
US20150045641A1 (en) 2013-03-13 2015-02-12 Optiscan Biomedical Corporation Method and apparatus for analyte measurement, display, and annotation
US9254092B2 (en) 2013-03-15 2016-02-09 Alivecor, Inc. Systems and methods for processing and analyzing medical data
CN103211603A (en) 2013-03-19 2013-07-24 江苏智诠传媒科技有限公司 Mental stress detecting, tracking and feedback system
WO2014165979A1 (en) 2013-04-11 2014-10-16 British Columbia Cancer Agency Branch Combined respiration and cardiac gating for radiotherapy using electrical impedance technology
ES2692666T3 (en) 2013-04-16 2018-12-04 Alivecor, Inc. Two-lead electrode device and methods for twelve-lead ECG
US9247911B2 (en) 2013-07-10 2016-02-02 Alivecor, Inc. Devices and methods for real-time denoising of electrocardiograms
US20150018660A1 (en) 2013-07-11 2015-01-15 Alivecor, Inc. Apparatus for Coupling to Computing Devices and Measuring Physiological Data
WO2015035251A1 (en) 2013-09-06 2015-03-12 Alivecor, Inc. Universal ecg electrode module for smartphone
US20150087952A1 (en) 2013-09-24 2015-03-26 Alivecor, Inc. Smartphone and ecg device microbial shield
US9420956B2 (en) 2013-12-12 2016-08-23 Alivecor, Inc. Methods and systems for arrhythmia tracking and scoring
CN103690166B (en) 2013-12-16 2016-06-08 天津科技大学 A kind of anti-imaging system of respiratory three-dimensional resistance based on PXI bus and formation method thereof
US10534900B2 (en) 2014-02-21 2020-01-14 Samsung Electronics Co., Ltd. Electronic device
EP3133984A4 (en) 2014-04-21 2017-12-27 Alivecor, Inc. Methods and systems for cardiac monitoring with mobile devices and accessories
US9652946B2 (en) 2014-05-02 2017-05-16 Novasentis, Inc. Hands-free, wearable vibration devices and method
US10028668B2 (en) 2014-05-06 2018-07-24 Alivecor, Inc. Blood pressure monitor
WO2016061513A1 (en) 2014-10-16 2016-04-21 The Arizona Board Of Regents Of Behalf Of The University Of Arizona Real-time vagal monitoring and intervention
KR20170078814A (en) 2014-11-04 2017-07-07 레스퍼러토리 모션 인코포레이티드 Respiratory parameter guided automated iv administration and iv tube clamp activation
WO2016127157A1 (en) 2015-02-08 2016-08-11 Zenso, Inc. System and method communicating biofeedback to a user through a wearable device
GB2537173B (en) 2015-04-10 2021-05-12 Huma Therapeutics Ltd Device and method for providing feedback on breathing rate.
EP3282933B1 (en) 2015-05-13 2020-07-08 Alivecor, Inc. Discordance monitoring
US10117598B1 (en) * 2015-11-08 2018-11-06 Sensogram Technologies, Inc. Non-invasive wearable respiration rate monitoring system
US10517531B2 (en) 2016-02-08 2019-12-31 Vardas Solutions LLC Stress management using biofeedback
TWI623298B (en) * 2016-03-25 2018-05-11 鋐雩科技有限公司 Wearable physiological measurement device
US10308257B2 (en) 2017-05-01 2019-06-04 Hitachi, Ltd. Monitoring respiration of a vehicle operator

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