• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
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  • 优先权
    • 专利摘要:
    In a method for generating and outputting a stimulus and / or a request for respiration for a human and / or an animal, wherein a heartbeat signal of the human or animal is received and transmitted to an evaluation unit (2), wherein the evaluation unit (2) within the Heartbeat signal is determined a predeterminable stimulus time range between two heartbeats, it is proposed that from the evaluation unit (2) generates a first stimulus and / or a first breath request at a first time (4) within the stimulus time range of a predetermined start heartbeat and on a signal unit (5) is transmitted, and that the signal unit (5) outputs the first stimulus and / or the first breath request in the form of a signal.
    公开号:AT515102A4
    申请号:T936/2013
    申请日:2013-12-04
    公开日:2015-06-15
    发明作者:
    申请人:Human Res Inst Für Gesundheitstechnologie Und Präventionsforschung Gmbh；
    IPC主号:
    专利说明:

    The invention relates to a method for producing and outputting a stimulus and / or a respiratory request for a human and / or an animal according to the preamble of patent claim 1.
    Heart rate variability refers to variations in a person's heart rate. This is influenced by numerous factors. It is known that there is an association between respiration and heart rate variability in positive emotional states, which has been described as "respiratory sinus arrhythmia". This relationship breaks down when there is stress or other stress.
    Various methods are currently known which aim to increase heart rate variability and cause a condition consistent with respiratory sinus arrhythmia, as it has been shown to lower this level of individual stress, for example, and to promote individual physical well-being. Such known methods cooperate in causing the subject concerned to perceive clearly positive states in such a way as to increase heart rate variability. However, these methods are dependent on the relationship of the subject to a supervisor or advisor, as well as the individual skills of the supervisor or consultant itself in terms of their effectiveness, and difficult to predict or reproducible.
    The object of the invention is therefore to provide a method of the type mentioned, with which the mentioned disadvantages can be avoided, and with which specifically the heart rate variability can be influenced.
    This is achieved by the features of claim 1 according to the invention.
    Thus, the heart rate variability can be trained specifically and effectively, this training is based solely on physically measurable effects. It has been found that by specifying stimuli or respiratory demands as described above, a targeted influencing of the heart rate variability of a subject can be achieved. As a result, a specific condition of a subject can be specifically caused, which affects both physically and psychologically on this. By suitable selection of the first time in the stimulus time range, as well as the nature of the stimulus, it is possible to specifi cally cause a particular condition in a subject. Thus, for instance, when an inhalation point is emitted within the so-called electrical diastole and inhalation of the subject at these times, a considerable increase in heart rate variability can be achieved. Thus, the well-being and performance of a subject can be sustainably and easily increased. This can improve the health of a subject. As a result, the increase in heart rate variability can be based on measurable effects, free from esoteric influences, as can still be observed in numerous courses on this topic. A training effect is measurably traceable. As a result, a point in time of breathing can be predetermined by metrological reasons, independent of non-reproducible influences, such as feelings, intuition or a so-called daily constitution. By subjecting the subject to targeted stimuli, such an effect can also be achieved without the active participation of the subject. Alternatively, however, the heart rate variability can also be deliberately reduced if a subject has too high a heart rate variability. This may be the case with people who suffer from a burnout syndrome or with a coma patient.
    The subclaims relate to further advantageous embodiments of the invention.
    The invention further relates to a device for generating and outputting a stimulus and / or a request for respiration for a human and / or an animal.
    The object of the invention is therefore to provide a device of the type mentioned above, with which the disadvantages mentioned above can be avoided, and with which specifically the heart rate variability can be influenced.
    This is achieved by the features of claim 1 according to the invention.
    Thereby, the advantageous effects set forth above for the method can be achieved.
    It is hereby expressly referred to the wording of the claims, whereby the claims at this point are incorporated by reference into the description and are considered to be reproduced verbatim.
    The invention will be described in more detail with reference to the accompanying drawings, in which only preferred embodiments are shown by way of example. Showing:
    Fig. 1 is a block diagram of a preferred embodiment of an objective device;
    2 shows an example of an ECG;
    3 shows a time course of the heart rate; and
    4 shows a detail of the view according to FIG. 2.
    The subject invention relates to a device 11 and a method for detecting and outputting a stimulus and / or a respiratory challenge. It is provided that measurements of at least one body function of a human or an animal are carried out, and that a signal is generated and output or displayed on the basis of these measurements. This signal is either a stimulus or a respiratory demand, therefore a request to the subject to inhale or exhale. In contrast to a stimulus, which involuntarily affects the subject, it is this at a respiratory demand, it may be both an inhalation request, as well as an exhalation request, even to follow this request.
    FIG. 1 shows a block diagram of a device 11 for determining and outputting a stimulus or a respiratory request, wherein the device 11 has a heart signal determination unit, an evaluation unit 2 and a signal unit 5 designed as an ECG unit 13. ECG 1 is the usual abbreviation for electrocardiogram. It is preferably provided that the heart signal determination unit is designed as an ECG unit 13. In the following, the invention will be described with regard to an ECG and an ECG unit 13, which, however, is preferably not restrictive. It has proved sufficient for simple implementations to detect only a so-called arterial pulse. It can be used as a heart signal and mechanical heart signal, such as a balistocardiogram and / or a Seismokardigramm. Preferably, a timely detection of the R-wave is considered sufficient.
    Furthermore, the term subject is used below, which preferably includes both animal and human subjects.
    The ECG unit 13 can be any type of ECG device or a device for generating an ECG 1, wherein it is provided in particular that the ECG unit 13 in question has a digital ECG unit 13 with a high time resolution and / or a high sampling rate, for example 8 kHz. Due to the high resolution, the R-wave of the ECG 1 can be detected better, whereby an accurate determination of the heart rate RR and consequently the heart rate variability HRV is possible. The ECG unit 13 is connected in circuit technology to inputs for ECG cable 12.
    The ECG unit 13 is further connected in circuit terms to the evaluation unit 2. The evaluation unit 2 is preferably a microcomputer system or a so-called embedded system, which preferably comprises a microcontroller. The evaluation unit 2 is designed to create or determine a stimulus and / or a respiratory request according to the method described below. It can also be provided to form the functionalities described below in the form of an ASIC.
    The evaluation unit 2 is connected to the signal unit 5, which is provided and designed to generate and output a stimulus or a respiratory request in the form of a signal after being controlled by the evaluation unit 2.
    The output of the stimulus or respiratory challenge is provided, in particular, to a signal means, such as a light source 14, such as an LED, and / or a loudspeaker 15. Correspondingly, the signal unit 5 is preferably formed comprising an analogue amplifier. It can also be provided, alternatively, optionally and / or additionally, to output the stimulus or the respiratory request in the form of a data packet, wherein provision is made for the signal unit 5 to have an interface, such as a USB port or a wireless interface, such as about Bluetooth, and having the corresponding driver circuits or controllers.
    With regard to the issue of the respiratory challenge is only relevant that this is recognized and understood by the subject as such. Relevant here is only that it is a clear and uniquely identifiable signal.
    This may vary depending on the region and culture.
    According to a preferred embodiment, it is provided that, when a breath request is issued, it is checked whether and / or after which breath latency time after delivery of the breath request the person and / or the animal is breathing. This can be checked for example by means of a suitably equipped with measuring devices, such as strain gauges, chest strap, which receives the contraction and expansion of the thorax and communicates with the evaluation unit in communication.
    Thus, a Atemlatenz time can be determined, therefore, a period of time, which passes from the discontinuation of the Atemaufforderung to the actual performance of the respiratory process by the subject. This breath latency time can subsequently be taken into account in the delivery of the breath request, for example by correcting the first time 4 by the breath latency time.
    A stimulus already acts unconsciously only in that the subject is or is exposed to this stimulus, whereby it is only relevant that the relevant stimulus is perceived by the subject. For this purpose, a monitoring of individual areas of the subject's senses may be provided.
    According to a first preferred embodiment, it is provided that the stimulus output as a signal is an optical stimulus, in particular a light stimulus, and that the signal is output as an optical signal. It is provided in particular that a specifiable color change and / or brightness change is used as a stimulus. Such an optical stimulus can be output by means of a monitor, for example. Preferably, for example, a change in the color of light to which the subject is exposed is provided from red to blue and / or green.
    According to a second preferred embodiment, it is provided that the stimulus output as a signal is an acoustic stimulus, and that the signal is output as an acoustic signal. In this case, provision is made in particular for a sound, a sound or a sound to be emitted, with predeterminable changes between tones,
    Noise and / or sounds of different volume, sound color, pitch, etc. may be provided. Also, a change between a sound and a sound can be provided.
    According to a third preferred embodiment, it is provided that the stimulus output as a signal is a tactile stimulus, and that the signal is output as a mechanical signal. In this case, provision is made in particular for the subject to be exposed to a predefinable change in vibration, or for example to be alternately touched in a predeterminable manner.
    According to a fourth preferred embodiment, it is provided that the stimulus emitted as a signal is an olfactory stimulus, and that the signal is output as the release of at least one perfume. In this case, it is provided in particular that in the region of the nose of the subject, it is possible to predeterminably release different fragrances in small quantities, and preferably each to be subsequently sucked off.
    In each case, it can be provided to check by means of suitable sensors, such as an eye camera, for example, if the subject is able to pick up the respective stimuli. It is also preferably provided to carry out a calibration before carrying out the method, which may also include a fundamental functional check of the intended purpose of each stimulus.
    In the method for generating and outputting a stimulus and / or a request for respiration for a human and / or an animal, it is provided that an ECG 1, a human or animal subject through an ECG device or an ECG unit 13 of a subject device 11 is recorded. It is provided that within the ECG 1 or the heartbeat signal, a prescribable stimulus time range is determined, which is arranged in the region between two heartbeats, such as between two R-waves.
    The stimulus time range may be any time range within a heartbeat signal that can be assigned to a specific heartbeat. According to the particularly preferred embodiment of the subject method described further below, provision is made in particular for the predefinable stimulus time range to be a time range of the electrical diastole 3. The following description is directed to it, it being possible to provide that the stimulus time range can be a different time range than the time range of the electrical diastole 3, and the corresponding description in this respect is preferably also applicable to other stimulus time ranges.
    The time range, which is generally referred to as electrical diastole 3, lies between the T-wave, or if present or detectable the U-wave, and the subsequent P-wave. The relevant time range of the electrical diastole 3 is shown in FIGS. 2 and 4. The determination of the time range of the electrical diastole 3 takes place in the evaluation unit 2, to which the ECG 1 is transmitted.
    In this case, provision is made in particular to determine a value for the time range of the electric diastole 3 by evaluating at least the interval between two R waves, preferably a predefinable plurality of consecutive R waves, and then the value thus determined for the time range of the electric Diastole 3 is also used for subsequent heartbeats or R-waves. In particular, it may be provided to characterize the time domain of the electrical diastole 3 by a pair of values consisting of a start time and an end time, which are each dimensioned by the R-wave preceding the relevant electrical diastole 3. Such characterization may also be provided for other selected stimulus time ranges.
    Various methods may be provided for detecting the region of the electrical diastole 3, wherein in particular it is intended to detect the R-waves, to determine the heart rate RR, therefore the time interval between two successive R-waves, and a certain time after one R wave, which time is dependent on the heart rate RR to assume the time range of the electric diastole 3. This is an approximate method, which, however, may be sufficient for the objective application, since in a first step it may be sufficient to detect a central region of the time range of the electrical diastole 3. In addition, this preferred method step is simple and can be implemented with only minor hardware requirements, and thus supports a mobile implementation of the subject device 11. It can also be provided to detect the relevant time range of the electrical diastole 3 more accurately by means of signal analysis, which is preferred for stationary Implementations of the method is provided.
    The evaluation unit 2 determines a first time 4 within the time range of the electrical diastole 3, and generates for a start heartbeat at this first time 4 a stimulus or a breath request, which is transmitted to the signal unit 5, which in turn outputs a corresponding signal. It is preferably provided that lie between the individual process steps described only the times required for electronic processing, and no signal buffer or the like are provided.
    The first time 4, which may also be referred to as the start time, designates the time within the time range of the electric diastole 3 at which or for which the stimulus or respiratory challenge is created or sent. The first time 4 may be indicated by its time interval to the R-wave of a heartbeat, in particular of the starting heartbeat.
    As a rule, a certain number of heartbeats pass between two breaths of a person. It is therefore provided that the evaluation unit 2 generates a second respiratory request at the first time 4 within the stimulus time range or the time range of the electrical diastole 3 of the heartbeat, which follows a prescribable number of heartbeats after the first heartbeat, and to the signal unit 5, and that the signal unit 5 outputs the second breath request in the form of a signal. It is preferably provided that the relevant number of heartbeats is initially given with a default value of approximately 6 to 8, which can be subsequently adapted. It has been shown that this leads to a phase-locked coupling of the subject method with the organism of the subject.
    As a result, the procedure can also take into account the present condition of the subject, and is significantly more effective than known methods which prescribe a waiting period independent of the organism of the subject between two breath requests. It has been shown that such a wait of a predeterminable number of heartbeats of the subject also has an advantageous effect on the output of stimuli, due to said coupling of the excitation with the organism of the subject.
    It has proved to be advantageous that the second stimulus and / or the second respiratory demand is different from the first stimulus or the first respiratory demand. For example, it may be provided to issue an inhalation request as the first respiratory request and to issue an exhalation request as the second respiratory request, or to expose the subjects to a red light as the first stimulus and blue light as the second stimulus. Depending on the nature of the stimulus or respiratory challenge, the number of heartbeats between the two stimuli or respiratory prompts may also be varied according to the preceding paragraph.
    It may be provided that the second stimulus, which is different from the first stimulus, is output at a different time within the stimulus time range than the first stimulus.
    Preferably, it is further provided that the first stimulus and / or the second stimulus are issued for a predeterminable stimulus period, wherein the relevant stimulus time period is, of course, smaller than the time duration of said number of heartbeats. Thus, for example, a first stimulus in the form of a vibration can be output at a first frequency, this first stimulus can be ended, and after a certain pause a second stimulus in the form of a second vibration can be output at a second, different frequency from the first.
    It is preferably provided that the first time 4 - at least initially - is selected approximately in the middle of the time range of the electric diastole 3. Already by a substantially arbitrary selection of the first time 4 within the time range of the electrical diastole 3, a significant improvement of the heart rate variability can be achieved. However, it has been shown that a further improvement is possible when carrying out the steps described below a particularly preferred embodiment of the subject method.
    It is preferably provided that a chronological progression of a heart rate RR is continuously determined from the ECG 1, therefore that the effect of the proposed exercise on the subject in question is continuously monitored. FIG. 3 shows an example of a time course 6 of the heart rate RR. In this case, the time t is plotted on the abscissa axis, and the heart rate RR on the ordinate axis. The zero point position on the ordinate axis is freely selectable, and can be predefined as a statistically known mean value of a typical heart rate RR, relative to which the heart rate RR measured in the test subject is entered. The individual points represent the respective measuring points for the individual measured heart rates RR.
    It is provided below to evaluate the time course 6 of the heart rate RR in terms of frequency and / or amplitude, wherein different methods in the time domain as well as in an image area can be provided.
    It is preferably provided that a value of a heart rate amplitude 9 is determined from the time course 6 of the heart rate RR. This heart rate amplitude 9 is also a value of the heart rate variability occurring at this time.
    For this purpose, it is preferably provided in which the time course 6 of the heart rate RR upper inflection points 7 and lower inflection points 8 are determined, and that the value of the heart rate amplitude 9 is determined from respectively successive upper and lower inflection points 7, 8. The determination of the upper inflection points 7 and lower inflection points 8 can take place approximately with the means of the curve discussion or the extreme value tasks.
    For this purpose, it is preferably provided that the first point in time 4 of the stimulus or the respiratory request within the time range of the electrical diastole 3, to determine a first amplitude associated with this first time 4, is kept constant for such a large number of successive heartbeats until an upper inflection point 7 and a lower inflection point 8 of the heart rate RR were detected. It can be provided to provide a stop criterion, if after an unexpectedly long time still no heart rate amplitude 9 could be determined.
    As an alternative to the above-described evaluation of the heart rate amplitude 9, it may be provided that a partial area, in particular between two measured heart rates RR, is differentiated in the time course 6 of the heart rate RR. Therefore, two measured heart rates RR are associated with a fictitious even whose slope is determined, and this quantity is considered as a target in the subject control loop.
    It is preferably provided in a further development that the first point in time 4 of the stimulus and / or the respiratory challenge is varied within the stimulus time range for determining a point in time at which a time course 6 of the heart rate RR with specifiable properties is determined. As already explained, the time range of the electrical diastole 3 has proven to be particularly advantageous for achieving a high heart rate amplitude 9. However, if a low or medium heart rate amplitude 9 is to be achieved or caused, other stimulus time ranges are advantageous.
    As already indicated, provision is made in particular for the first time 4 of the stimulus or the respiratory challenge to be varied within the time range of the electrical diastole 3, for determining a heart rate amplitude maximum time 10 at which a maximum of the heart rate amplitude 9 has been determined is or prevails, whereby the effect of the exercises performed can be further increased.
    Furthermore, it is preferably provided that the first time 4 is varied within a predeterminable grid. Therefore, it is envisaged that only a discrete and limited number of variations will be made to quickly get a good result as well as to avoid endless loops. This supports both the implementation of the method as well as its implementability, especially in mobile applications.
    The described determination of a heart rate amplitude maximum time 10 is an iterative method, which is intended to abort after a predeterminable number of variations, and the first time 4 known at that point with the highest value of heart rates hitherto Amplitude 9 as the heart rate amplitude maximum time 10. This can ensure that a heart rate amplitude maximum time 10 is actually determined. In FIG. 4, both a first time 4 and a heart rate amplitude maximum time 10 are entered by way of example.
    As soon as the heart rate amplitude maximum time 10 has been determined or determined, it is provided to generate the stimulus or respiratory prompts at the heart rate amplitude maximum time points 10 and transmit them to the signal unit 5, so that the test person now uses the Respiratory prompts at the times signaled or the stimulus is issued at the relevant times, which promise the highest training effect.
    To adapt to changes in the subject or to take into account a possible drift of the heart rate amplitude maximum time 10, it is preferably provided that after a predetermined number to the heart rate amplitude maximum time 10 issued stimuli or respiratory demands, the stimulus or ., The respiratory demand in a predeterminable temporal environment around the heart rate amplitude maximum time 10 is specifially varied. It is preferably provided that the respective temporal environment has a temporally small duration compared to the time duration of the electric diastole 3.
    In a further development, it is provided that the heart rate amplitude maximum time 10 is adjusted to this new time when a new time of a maximum of the heart rate amplitude 9 is determined. This ensures a stable and effective training over a longer period of time.
    claims:
    权利要求:
    Claims (25)
    [1]
    DR. FERDINAND GIBLER ΛΙΠΙ CDP DOTU DR DR. WOLFGANG POTH OIDLIIKvX Γ VI Π Austrian and European Patent and Trademark Attorneys HAI tN lANWALI t PATENT CLAIMS 1. Method of producing and issuing a stimulus and / or a breath request for a human and / or an animal, wherein a heartbeat signal of the human or animal is received and transmitted to an evaluation unit (2), wherein the evaluation unit (2) within the heartbeat signal, a predeterminable stimulus time range between two heartbeats is determined characterized in that generated by the evaluation unit (2) a first stimulus and / or a first breath request at a first time (4) within the stimulus time range of a predetermined start heartbeat and transmitted to a signal unit (5), and that the Signal unit (5) outputs the first stimulus and / or the first breath request in the form of a signal.
    [2]
    2. The method according to claim 1, characterized in that the heartbeat signal is an ECG (1).
    [3]
    3. The method according to claim 1 or 2, characterized in that the predeterminable stimulus time range is a time range of the electrical diastole (3).
    [4]
    4. The method according to any one of claims 1 to 3, characterized in that the respiratory request is an inhalation request and / or a Ausatemaufforderung.
    [5]
    5. The method according to any one of claims 1 to 4, characterized in that the, emitted as a signal stimulus is an optical stimulus, and that the signal is output as an optical signal.
    [6]
    6. The method according to any one of claims 1 to 5, characterized in that the, emitted as a signal stimulus is an acoustic stimulus, and that the signal is output as an acoustic signal.
    [7]
    7. The method according to any one of claims 1 to 6, characterized in that the output as a signal stimulus is a tactile stimulus, and that the signal is output as a mechanical signal.
    [8]
    8. The method according to any one of claims 1 to 7, characterized in that the emitted as a signal stimulus is an olfactory stimulus, and that the signal is issued as the release of at least one perfume.
    [9]
    9. The method according to any one of claims 1 to 8, characterized in that of the evaluation unit (2) a second stimulus and / or a second respiratory demand at the first time (4) within the stimulus time range of, a predetermined number of heartbeats after the first heartbeat subsequent heartbeat generated and transmitted to the signal unit (5), and that the signal unit (5) outputs the second stimulus and / or the second breath request in the form of a signal.
    [10]
    10. The method according to claim 9, characterized in that the second stimulus and / or the second respiratory demand is different from the first stimulus or the first respiratory demand.
    [11]
    11. The method according to any one of claims 1 to 10, characterized in that from the heartbeat signal, in particular the ECG (1) continuously a time course (6) of a heart rate (RR) is determined,
    [12]
    12. The method according to claim 11, characterized in that the time course (6) of the heart rate (RR) is evaluated in terms of frequency and amplitude.
    [13]
    13. The method of claim 11 or 12, characterized in that from the time course (6) of the heart rate (RR) a value of a heart rate amplitude (9) is determined.
    [14]
    14. The method of claim 11,12 or 13, characterized in that in the time course (6) of the heart rate (RR) upper inflection points (7) and lower inflection points (8) are determined, and that from each successive upper and lower Turning points (7, 8), the value of the heart rate amplitude (9) is determined.
    [15]
    15. The method according to claim 14, characterized in that the first time (4) of the stimulus and / or the breath request within the stimulus time range for such a successive heartbeats is kept constant until an upper inflection point (7) and a lower inflection point (8) the heart rate were detected.
    [16]
    16. The method according to any one of claims 11 to 15, characterized in that a partial area, in particular between two measured heart rates (RR), in the time course (6) of the heart rate (RR) is differentiated.
    [17]
    17. The method according to any one of claims 1 to 16, characterized in that, when issuing a request for respiration, it is checked whether and / or after which respiratory latency time after delivery of the respiratory request the person and / or the animal is breathing.
    [18]
    18. The method according to claim 17, characterized in that the first time (4) is corrected by the Atemlatenz time.
    [19]
    19. The method according to any one of claims 11 to 18, characterized in that the first time (4) of the stimulus and / or the respiratory challenge within the stimulus time range is varied, for determining a time at which a time course (6) of the heart rate (RR) is determined with specifiable properties.
    [20]
    20. The method according to claim 19, characterized in that the first time (4) is varied to determine a heart rate amplitude maximum time (10) at which a maximum of the heart rate amplitude (9) is detected.
    [21]
    21. The method according to claim 19 or 20, characterized in that the first time (4) is varied within a predeterminable grid.
    [22]
    22. The method according to claim 20 or 21, characterized in that generated after determination of the heart rate amplitude maximum time (10) of the stimulus and / or the breath requests at the heart rate amplitude maximum time points (10) and to the signal unit be transmitted.
    [23]
    23. The method according to any one of claims 20 to 22, characterized in that after a predetermined number to the heart rate amplitude maximum time (10) output stimuli and / or Atemaufforderungen, the stimulus and / or the Atemaufforderung in a predeterminable temporal environment the heart rate amplitude maximum time (10) is specifially varied.
    [24]
    24. The method according to any one of claims 20 to 23, characterized in that the heart rate amplitude maximum time (10) is adjusted upon determination of a new time of a maximum of the heart rate amplitude (9) at this new time.
    [25]
    25. Device (11) for generating and outputting a stimulus and / or a respiratory request for a human and / or an animal, wherein the device (11) comprises a cardiac signal determining unit, in particular an ECG unit (13), an evaluation unit (2) and a signal unit (5), wherein the heart signal detection unit with signal inputs and with the evaluation unit (2) is connected, and wherein the evaluation unit (2) to the signal unit (5) is connected, characterized in that the evaluation unit (2) is formed a To create stimulus and / or a request for breathing, in particular according to one of claims 1 to 24.

    Gibler & Poth Patent Attorneys OG (Dr. F. Gibler or Dr. W. Poth)
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    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    JP2010088607A|2008-10-07|2010-04-22|Olympus Corp|Heart stimulating device|
    KR20130087940A|2012-01-30|2013-08-07|동서대학교산학협력단|An hrv detecting method and the hrv detection device|
    US7713212B2|2003-11-03|2010-05-11|Coherence Llc|Method and system for consciously synchronizing the breathing cycle with the natural heart rate cycle|
    US9132333B2|2008-06-06|2015-09-15|Koninklijke Philips N.V.|Method and system for maintaining a state in a subject|
    EP2311533A1|2009-10-13|2011-04-20|Koninklijke Philips Electronics N.V.|Respiration controlling apparatus|AT517071B1|2015-08-28|2016-11-15|Human Res Inst Für Gesundheitstechnologie Und Präventionsforschung Gmbh|Method and device for determining at least one cardiac load duration and / or a cardiac recovery period from a heartbeat signal|
    JP6479720B2|2016-08-30|2019-03-06|株式会社電通|Meditation assistance device and meditation assistance system|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    ATA936/2013A|AT515102B1|2013-12-04|2013-12-04|Method and device for generating and outputting a stimulus and / or a request for respiration for a human and / or animal|ATA936/2013A| AT515102B1|2013-12-04|2013-12-04|Method and device for generating and outputting a stimulus and / or a request for respiration for a human and / or animal|
    ES14833106T| ES2881545T3|2013-12-04|2014-12-04|Procedure and device for the creation and emission of a stimulus and / or a breathing instruction for a human being and / or an animal|
    PCT/AT2014/000216| WO2015081355A1|2013-12-04|2014-12-04|Method and device for creating and outputting a stimulus and/or an instruction to breathe for a person and/or an animal|
    EP14833106.9A| EP3077066B1|2013-12-04|2014-12-04|Method and device for creating and outputting a stimulus and/or an instruction to breathe for a person and/or an animal|
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