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WO2006113879A2 - Systeme et procede pour detecter un changement incontrolable dans la physiologie d'une personne - Google Patents

Systeme et procede pour detecter un changement incontrolable dans la physiologie d'une personne Download PDF

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Publication number
WO2006113879A2
WO2006113879A2 PCT/US2006/014911 US2006014911W WO2006113879A2 WO 2006113879 A2 WO2006113879 A2 WO 2006113879A2 US 2006014911 W US2006014911 W US 2006014911W WO 2006113879 A2 WO2006113879 A2 WO 2006113879A2
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WO
WIPO (PCT)
Prior art keywords
person
sensor assembly
baseline
processing unit
structured
Prior art date
Application number
PCT/US2006/014911
Other languages
English (en)
Other versions
WO2006113879A3 (fr
Inventor
Hector Jose Estrella
Original Assignee
Malloy & Malloy, P.A.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Malloy & Malloy, P.A. filed Critical Malloy & Malloy, P.A.
Publication of WO2006113879A2 publication Critical patent/WO2006113879A2/fr
Publication of WO2006113879A3 publication Critical patent/WO2006113879A3/fr

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/16—Devices for psychotechnics; Testing reaction times ; Devices for evaluating the psychological state
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/02—Detecting, measuring or recording for evaluating the cardiovascular system, e.g. pulse, heart rate, blood pressure or blood flow
    • A61B5/0205—Simultaneously evaluating both cardiovascular conditions and different types of body conditions, e.g. heart and respiratory condition
    • A61B5/02055—Simultaneously evaluating both cardiovascular condition and temperature
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/16—Devices for psychotechnics; Testing reaction times ; Devices for evaluating the psychological state
    • A61B5/165—Evaluating the state of mind, e.g. depression, anxiety
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/48—Other medical applications
    • A61B5/4866—Evaluating metabolism
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/0002—Remote monitoring of patients using telemetry, e.g. transmission of vital signals via a communication network
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/02—Detecting, measuring or recording for evaluating the cardiovascular system, e.g. pulse, heart rate, blood pressure or blood flow
    • A61B5/021—Measuring pressure in heart or blood vessels
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/02—Detecting, measuring or recording for evaluating the cardiovascular system, e.g. pulse, heart rate, blood pressure or blood flow
    • A61B5/024—Measuring pulse rate or heart rate
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/08—Measuring devices for evaluating the respiratory organs
    • A61B5/0816—Measuring devices for examining respiratory frequency
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/117—Identification of persons
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/145—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/24—Detecting, measuring or recording bioelectric or biomagnetic signals of the body or parts thereof
    • A61B5/316—Modalities, i.e. specific diagnostic methods
    • A61B5/389—Electromyography [EMG]

Definitions

  • the present invention relates to a system for the detection of an uncontrollable change in a person's physiology, such as occurs in a person experiencing fear or an orgasm. More in particular, the present invention comprises a sensor assembly structured to monitor at least one bodily function during a baseline monitoring period and an activity monitoring period, and a central processing unit structured to interpret activity data obtained from the sensor assembly, and in particular, to detect a predetermined change in the at least one bodily function during the activity monitoring period.
  • the system may also comprise an output device structured to provide an indication when the predetermined change in bodily function is detected.
  • the present invention also teaches a method for the detection of an uncontrollable change in a person's physiology, such as occurs during orgasm or when a person experiences fear.
  • one such diagnostic device comprises a glove member structured to fit on a user's hand which is interconnected via a transmission cable to an interface/command center.
  • the glove member includes a variety of diagnostic sensors structured to measure such parameters as EKG, blood pressure, pulse rate, and/or temperature.
  • This device may also be structured to allow measurement of blood oxygen levels as well as the detection of sound waves generated by the patient's heart and lungs when the glove member is positioned over the chest of the user, via an auscultation device.
  • the interface/command center is structured to transmit the data collected to a remote location, for example, via an internet connection, wherein the data is interpreted by trained personnel, such as a doctor or nurse, who then provide medical advice and/or instruction to the user.
  • the device provides a means for a person to measure the values of a variety of bodily functions
  • the device requires the person to be physically interconnected to the interface/command center via the cable, which limits use of the device to locations where such an interface/command center is located, and further limits the data collected to the brief period of time in which the person is physically interconnected.
  • the aforementioned device permits the collection of data corresponding to the various bodily functions, it requires trained personnel to interpret the data collected before it is of value to the user.
  • a number of portable devices have also been developed which allow a user to measure various bodily functions.
  • One such device permits the user to monitor such bodily functions as blood pressure, temperature, and pulse rate, and includes a display screen to provide the user with real time data.
  • This device also allows for the storage of data collected over a period of time for retrieval and analysis at a later time, such as may be requested or required by trained medical personnel .
  • Other portable devices include an electrocardiogram monitor which allow a user to monitor their electrocardiogram on a viewable screen, and a cardiac meter which is structured to be worn on a user's wrist.
  • Such portable devices afford a user a degree of privacy while monitoring certain bodily functions, and it is known that monitoring of bodily functions in private may be desirable in certain instances. For example, while monitoring the bodily functions of a person engaged in sexual activity, certain person's may prefer or in fact insist that such monitoring be conducted privately.
  • At least one device has been developed to identify a contraction of certain muscles in an attempt to determine the occurrence of an orgasm of the user.
  • the device is structured to identify the contraction of the anal sphincter and associated muscles of the person being monitored. While it appears that this device may be utilized in private by the user, the device must be inserted into the anal canal , which many users may find overly intrusive and/or uncomfortable, particularly while engaging in sexual activity, thereby precluding widespread usage and benefit .
  • a system which may be utilized in private by a user to monitor one or more bodily functions while the person is engaged in various activities, such as sexual activity. It would further be helpful if such a system allowed the bodily functions to be monitored in a non-intrusive manner, to assure widespread acceptance and usage of any such system. Additionally, such a system would preferably provide the user with results which are interpreted without requiring the assistance of specially trained personnel and/or equipment. More specifically, it would be beneficial to provide a system which allows a user to monitor and detect uncontrollable changes in certain bodily functions which are indicative of a particular sensation a person is experiencing, such as fear or an orgasm.
  • the present invention is directed to a system for detecting an uncontrollable change in a person's physiology.
  • the system comprises a sensor assembly which is disposed in a monitoring relation with the person. More in particular, the sensor assembly comprises at least one sensor structured to monitor at least one preselected bodily function of the person during an activity monitoring period, however, in at least one embodiment, the sensor assembly comprises a plurality of sensors structured to monitor a plurality of bodily functions.
  • the sensor assembly may be physically attached to one or more portions of the person's body, or it may be structured to monitor the bodily function or functions of the person remotely, such as, by way of example only, via infrared, microwave, optical, sound or light waves, or other remote signal.
  • the sensor assembly may be structured to monitor one or more of a plurality of bodily functions including, but not limited to blood pressure, pulse, temperature, respiration, muscular contractions, caloric expenditure, blood oxygen level, release of sweat and/or other components such as endorphins, pheromones, adrenaline, etc., as well as sound waves generated either vocally or via the pulse, heart beat, and/or respiration of the person being monitored.
  • bodily functions including, but not limited to blood pressure, pulse, temperature, respiration, muscular contractions, caloric expenditure, blood oxygen level, release of sweat and/or other components such as endorphins, pheromones, adrenaline, etc., as well as sound waves generated either vocally or via the pulse, heart beat, and/or respiration of the person being monitored.
  • the present invention also includes a central processing unit which is disposed in a communicating relation with the sensor assembly, which is to say that the sensor assembly is structured to transfer at least one activity data set to the central processing unit corresponding to the at least one preselected bodily function being monitored during the activity monitoring period.
  • the sensor assembly is structured to transfer a plurality of activity data sets, each corresponding to a different one of the preselected bodily functions being monitored during the activity monitoring period.
  • the sensor assembly may be structured to transfer a plurality of activity data sets, each corresponding to a different one of the preselected bodily functions being monitored during each of a different one of a plurality of activity monitoring periods.
  • the central processing unit is structured to interpret each activity data set transferred by the sensor assembly and to detect a predetermined change in the preselected bodily function to which each activity data set corresponds.
  • the system may include an output device which is operatively associated with the central processing unit and is structured to generate an indication upon detection of the predetermined change in one or more of the preselected bodily functions, by the central processing unit.
  • the central processing unit comprises a data memory module structured to store at least one, but preferably a plurality of activity data sets, each corresponding to one of the plurality of bodily functions monitored during each of a plurality of activity monitoring periods .
  • the data memory module is further structured to permit the central processing unit to correlate each of the plurality of activity data sets.
  • the central processing unit comprises an external data transmission port structured to transmit the plurality of activity data sets to an external data processing device to provide additional storage and facilitate further analysis of the plurality of activity data sets.
  • the system of the present invention in at least one embodiment, is utilized to measure an uncontrollable change in the physiology of other living creatures including, but not limited to dogs, cats, mice, rats, birds, and horses, among others.
  • the bodily functions and/or parameters which may be obtained and/or monitored utilizing the system of the present invention may further include Shockwaves, electrowaves, brainwaves, and/or the aura generated by the person.
  • the system may utilize hair recognition technology to detect the size, diameter and/or length, density, color, etc, of the hair located on a portion of the person's body.
  • system may comprise the measurement of geometrical and special dimensions of various portions of the person's body including, but not limited to measurement of the person's nose, ears, eyes, penis, or vagina, just to name a few.
  • One further embodiment of the present invention provides for the measurement and monitoring of the amount of heat absorbed or heat released by the person's body.
  • the system may be utilized to measure and monitor fluids, hormones, proteins, gases, odors, particulate matter, sounds and/or sound waves expelled from or absorbed by the person's body, including macro-, micro-, and/or nano-measurement of the same .
  • At least one other embodiment of the system may be utilized for the detection of any contraction of the body, including contractions of the muscles and/or organs, as well as any voluntary and/or involuntary movement or contraction of the body, such as may be detectible by a motion sensor or otherwise.
  • the system of the present invention may also be utilized to monitor, measure, and calculate the amount, concentration, rate of absorption or adsorption, rate of expulsion, degree of contraction, and/or frequency (where applicable) of at least the physical parameters identified herein. Any number of the physical parameters identified herein may also be present and monitored in the environment surrounding the person being monitored.
  • One other embodiment of the present invention may be utilized to monitor skin color, hair color, stains, physiological and/or biological changes in the body due to illness or external stimuli.
  • the values of any the parameters detected, monitored, stored, and/or analyzed by at least one embodiment of the system of the present invention may be expressed in terms of percentages, exact amounts, estimated or approximated amounts, and/or scaled values.
  • the system has storage capability for the baseline and activity data sets, the baseline and activity biometric parameters, and any calculated values generated utilizing the same, which may be stored and/or transmitted by the system.
  • At least one embodiment of the system of the present invention includes capacity for wired and/or wireless data transmission for receiving and/or transmitting data to or from external 'devices including, but not limited to, external processing units and/or external output devices. More specifically, the system is capable of exchanging data with any external equipment or mechanism.
  • the sensor assembly in at least one embodiment may utilize laser, infrared, ultraviolet, or other electromagnetic radiation waves, magnetic, non-magnetic, electrical, audible, or visual energy to effect wireless data and/or signal transmission between components of the system.
  • One further embodiment of the present invention may be comprise a secure activation mechanism utilizing a biometric identification device to measure any of a variety of biometric parameters including, but not limited to, fingerprint patterns, iris patterns, voice and/or other sound patterns, wave energy- patterns emitted form the body, hair patterns, including density, color, size, i.e. diameter and/or length, skin porosity patterns, geometrical and spatial dimensions of portions of the person's body, and respiration patterns, just to name a few.
  • Other biometric parameters may include biological secretions from the body, and energy waves generated by the body, for example, the person's aura.
  • the system of the present invention may further employ barcodes, magnetic, and/or non-magnetic systems to secure access and activation of the system.
  • the system may further provide for encryption and decryption of the data received, transmitted, stored, analyzed, or otherwise utilized by the system.
  • Yet one further embodiment of the system of the present invention comprises internal or external global positioning technology, cellular and non-cellular communications capacity, and is structured to store and play any media which may be scanned and/or read into the system in any data format .
  • the present invention also provides a method for detecting an uncontrollable change in a person's physiology. Specifically, the method comprises monitoring at least one preselected bodily function of the person during an activity monitoring period, and transferring an activity data set corresponding to the preselected bodily function for analysis. At least one embodiment of the present invention provides for monitoring a plurality of preselected bodily functions during the activity monitoring period.
  • the method also provides for interpreting one or more one activity data sets by comparing each activity data set to a table containing a value or range of values of a predetermined change in one or more preselected bodily functions being monitored and detecting a predetermined change in the preselected bodily function to which each activity data set corresponds.
  • the method comprises interpreting each of the plurality of activity data sets via a central processing unit and detecting the predetermined change. Additionally, the method of the present invention may comprise generating an indication upon detection of the predetermined change in the at least one preselected bodily function.
  • Figure 1 is a schematic view of one embodiment of a system of the present invention.
  • Figure 2 is a schematic view of one embodiment of a sensor assembly of the system of the present invention.
  • Figure 3 is a schematic view of one other embodiment of a sensor assembly of the system of the present invention.
  • Figure 4 is a schematic view of yet another embodiment of a sensor assembly of the present invention.
  • Figure 5 is a side elevation of one embodiment of an output device of the present invention.
  • Figure 6 is a front elevation of another embodiment of an output device of the present invention.
  • the present invention is directed to a system, generally as shown at 10, for detecting an uncontrollable change in a person's physiology.
  • person's have been known to control and/or mask measurable changes in certain bodily functions, for example, pulse and/or respiration rates, under numerous and varied conditions such as physical stress, exertion, etc.
  • certain sensations can result in measurable changes in one or more of these bodily functions which are involuntary or uncontrollable.
  • a person experiencing the sensation of fear exhibits measurable changes in certain bodily functions which cannot be controlled or masked.
  • the system 10 of the present invention permits the detection of these uncontrollable changes in bodily function (s) , and as a result, it allows detection of a particular sensation which a person is experiencing, including, by way of example only, fear or orgasm.
  • the system 10 comprises a sensor assembly, generally illustrated at 20, disposed in a monitoring relation to the person.
  • the sensor assembly 20 comprises at least one sensor structured to monitor at least one preselected bodily function of the person during a baseline monitoring period.
  • the baseline monitoring period comprises a period when the person is not exposed to any stimuli which may alter the normal value of the preselected bodily function during the baseline monitoring period. More in particular, the person should be in their normal state of health and should be at rest and not engaged in any physical or mental activity, or exposed to any excessive environmental conditions such as lighting, temperature, or noise levels, such that the data obtained during the baseline monitoring period establish the normal values of the preselected bodily function for that person.
  • the sensor assembly 20 comprises a plurality of sensors structured to monitor a plurality of preselected bodily functions of the person during the baseline monitoring period, thereby establishing normal values for a plurality of preselected bodily functions for that person.
  • the sensor assembly 20 is further structured to monitor at least one preselected bodily function of the person being monitored during an activity monitoring period.
  • the activity monitoring period is any period of time during which the person is exposed to a particular form of stimulation including, by way of example only, the period of time during which a person is engaged in sexual activity, preferably including at least an amount time both before and after the person experiences the sensation of an orgasm.
  • the sensor assembly 20 comprises a plurality of sensors structured to monitor a plurality of preselected bodily functions during the activity monitoring period.
  • the sensor assembly 20 is structured to monitor one or more of the plurality of preselected bodily functions during each of a plurality of activity monitoring periods.
  • the preselected bodily functions of the person which may be monitored by the sensor assembly 20 of the present invention may include, but are in no way limited to, blood pressure, pulse, temperature, respiration, muscular contractions, caloric expenditure, blood oxygen level, release of sweat and/or other components such as endorphins, pheromones, adrenaline, etc., as well as sound waves generated either vocally or via pulse, heart beat, and/or respiration of the person being monitored. It is understood that other bodily functions exhibit uncontrollable changes when a person experiences certain sensations, and the scope of the system 10 of the present invention encompasses monitoring such other preselected bodily functions to allow detection of other sensations which the person may experience.
  • the sensor assembly 20 of the present invention is structured to detect at least one, but preferably a plurality of preselected bodily functions, and as such, the sensor assembly 20 comprises at least one, but preferably a plurality of detectors, each of which is disposed in a communicative relation to the person being monitored.
  • the sensor assembly 20 comprises a temperature detector or thermal sensor 21, a blood pressure detector 22, and a pulse rate detector 23. It is understood, however, that other embodiments of the sensor assembly 20 of the present invention may comprise either additional or alternate detectors, as illustrated in Figures 3 and 4, respectively.
  • Figure 3 illustrates the sensor assembly 20 of Figure 2 further comprising an oxygen detector or oximeter 24, structured to monitor the person's blood oxygen level, and an electrocardiograph detector 25, structured to monitor the person's cardiovascular activity during the baseline and activity monitoring periods.
  • the sensor assembly 20 may comprise a respiration rate detector 26, an electromyograph detector 27, structured to monitor a frequency of muscular contraction of the person, and a caloric expenditure detector or calorimeter 28, structured to monitor the amount of calories expended by the person during a baseline monitoring period as well as during an activity monitoring periods, and more in particular, during at least a portion thereof.
  • the plurality of detectors 21 through 25 physically engage the person and are structured to transmit electrical, optical, audible, and/or other signals to the sensor assembly 20 via a plurality of signal carriers 20' which may include, by way of example only, electrical wires or fiberoptic cables, thereby establishing a data communicative relationship with the sensor assembly 20.
  • the sensor assembly 20 is disposed in a remote monitoring relation to the plurality of detectors 21 through 25, which physically engage the person being monitored.
  • the "remote monitoring relation" as used herein is at least partially defined by the sensor assembly 20 being disposed in a wireless data communicative relationship with the plurality of detectors, including at least detectors 21 through 28, via one or more remote signals 29 which are transmitted between the plurality of detectors 21 through 28 and the sensor assembly 20 without requiring a physical connection between the sensor assembly 20 and the plurality of detectors 21 through 28, such as, by way of example only, an electrical wire or a fiberoptic cable.
  • an infrared signal may be utilized to remotely and non-intrusively monitor and transfer data corresponding to the person's body temperature via the temperature detector or thermal sensor 21, without requiring a physical wired connection between the temperature detector or thermal sensor 21 and the sensor assembly 20.
  • a sound or light wave may be remotely and non-intrusively directed towards the person's body and the person's blood pressure may be remotely monitored and transferred from the blood pressure detector 22 to the sensor assembly 20 via a remote Doppler signal, resulting from the Doppler effect on the reflected sound or light.
  • Yet another example may include various optical signals transmitted to and/or from the person's body, either directly or to one or more detectors interconnected thereto, which allows the sensor assembly 20 to remotely monitor any number of other preselected bodily functions.
  • the remote monitoring relation of the sensor assembly 20 with the person may be particularly desirable in certain applications wherein physical interconnection between the plurality of detectors 21 through 28 and the sensor assembly 20, such as by electrical wires or fiberoptic cables, as illustrated in Figure 2, may detract from the overall sensation the person is experiencing.
  • the detraction resulting from the physical interconnection to the sensor assembly 20 may be exceptionally bothersome, for example, during sexual activity, particularly during the period of time before and after orgasm.
  • the system 10 of the present invention further comprises a central processing unit, generally as shown at 30, disposed in a communicating relation with the sensor assembly 20. More specifically, the sensor assembly 20 is structured to transfer a baseline data set and at least one activity data set to the central processing unit 30 which correspond to the values of at least one bodily function of the person being monitored during the baseline monitoring period and at least one activity monitoring period.
  • each baseline and/or activity data set may further comprise, by way of example only, an identifier of the bodily function, date and/or time stamps for each value of the bodily function obtained, and other identifying information as may be necessary to permit efficient interpretation of the baseline and/or activity data set.
  • At least one biometric parameter of the person is associated with specific baseline and activity data sets, thereby providing a means to secure access to the person's data by requiring identification and verification of the biometric parameter as a condition to access the data sets.
  • each activity data set may comprise an audio and/or video data component.
  • the sensor assembly 20 may transfer the baseline and activity data sets to the central processing unit 30 via any one of a number of data transmission mechanisms including, by way of example only, hard wired connections or any of the myriad of wireless transmission mechanisms utilizing remote signals 29 including, by way of example only, light and/or sound waves. Further, in one preferred embodiment, the sensor assembly 20 is structured to transfer the baseline and activity data sets to the central processing unit 30 as a continuous data stream thereby approximating real time data which the central processing unit 30 interprets .
  • the sensor assembly 20 may be structured to transfer a plurality of baseline data sets and a plurality of activity data sets to the central processing unit 30 wherein each of the plurality of baseline and activity data sets corresponds to a different one of a plurality of bodily functions being monitored during the baseline and activity monitoring periods.
  • the sensor assembly 20 is structured to transfer a plurality of activity data sets to the central processing unit 30, wherein each of the plurality of activity data sets corresponds to at least one bodily function being monitored during each of a different one of a plurality of activity monitoring periods.
  • the sensor assembly 20 is structured to transfer a plurality of activity data sets each corresponding to one of a plurality of bodily functions being monitored during each of different ones of a plurality of activity monitoring periods.
  • the central processing unit 30 of the present invention is structured to interpret at least each baseline data set and each activity data set transferred by the sensor assembly 20 and to detect a predetermined change in the preselected bodily function between the baseline monitoring period and the activity monitoring period for which each activity data set corresponds.
  • the central processing unit 30 comprises a data memory module 35 which is structured to store at least one baseline data set, and a value or range of values of a predetermined change corresponding to at least one preselected bodily function.
  • the central processing unit 30 comprises a data memory module 35 structured to store a plurality of values or ranges of values of a predetermined change each corresponding to a different one of a plurality of preselected bodily functions.
  • the central processing unit 30 is further structured to compare each activity data set with the value or range of values of the predetermined change for the preselected bodily function corresponding to the activity data set, and to detect each predetermined change therefrom.
  • the central processing unit 30, in one preferred embodiment, is further structured to identify the magnitude or intensity of each predetermined change detected.
  • the data memory module 35 of the present invention may also be structured to store at least select ones of the baseline data sets and the plurality of activity data sets transferred to the central processing unit 30 by the sensor assembly 20. Further, the data memory module 35 of the present invention may be structured to store the baseline and activity data sets which correspond to plurality of persons. In addition, the data memory module 35 may be structured to store the results for one or more of the predetermined changes detected by the central processing unit 30, either alone or in combination with the corresponding activity data set in which the predetermined change was detected.
  • At least one embodiment of the central processing unit 30 of the present invention comprises an external data transmission port 37 structured to transmit at least one but preferably a plurality of baseline and activity data sets to an external data processing device, such as, by way of example only, a personal computer, laptop computer, or personal digital assistant, to provide additional data storage capacity and/or to facilitate further processing of the plurality of baseline and activity data sets, either in real time or at a future time selected by the user.
  • an external data processing device such as, by way of example only, a personal computer, laptop computer, or personal digital assistant, to provide additional data storage capacity and/or to facilitate further processing of the plurality of baseline and activity data sets, either in real time or at a future time selected by the user.
  • the external data processing device may be structured to store, in addition to the baseline data set and the plurality of activity data sets, the results for one or more of the predetermined changes detected, either alone or in combination with the corresponding activity data set in which the predetermined change was detected.
  • the external data processing device may be utilized to facilitate comparison of various activity data sets collected during a plurality of discreet periods of time, occurring, perhaps, over a period of years, which will allow the user to compare the intensity of the predetermined changes detected under a variety of different circumstances, as well as to identify trends and/or potential shifts in the value or range of values of the predetermined change in the preselected bodily functions being monitored.
  • the central processing unit 30 is structured to detect a predetermined change in the blood pressure of the person being monitored, and more specifically, an increase in blood pressure.
  • the predetermined change may correspond to an increase in the person's blood pressure in a range of between approximately 30 to 40 millimeters of mercury.
  • the central processing unit 30 is structured to detect a predetermined change in the pulse rate of the person being monitored.
  • the predetermined change may be an increase in pulse rate in a range of between approximately 20 to 30 beats per minute.
  • the central processing unit 30 is structured to detect a predetermined change in body temperature such as, again, by way of example only, an increase in a range of between approximately 0.75 to 1.25 degrees Fahrenheit.
  • Additional predetermined changes which the central processing unit 30 of the present invention may be structured to detect may include, but are not limited to, an increase in frequency of a muscular contraction, and in particular a muscular contraction in at least one pelvic muscle, wherein a predetermined change may be in a range of, for example, between approximately 1.0 to 1.5 cycles per second, or an increase in an amount of caloric expenditure, wherein a predetermined change may be, once again by way of example, in a range of between approximately 450 to 500 calories, during at least a portion of the specified period, such as, during an orgasm.
  • the aforementioned ranges of values for predetermined changes are solely for illustrative purposes.
  • the value or range of values for a predetermined change of a bodily function may vary from person to person depending on such factors as their respective ages, weights, health, etc., and may be higher or lower or encompass a broader or narrower ranges between different persons.
  • the value or range of values for a predetermined change of a particular bodily function may vary for the same person depending on such factors as their age, level of physical activity, stress, health, etc., and once again may be higher or lower or encompass a broader or narrower range .
  • the value or range of values of the predetermined change of a bodily function may be set and/or reset by user input to the central processing unit 30.
  • the central processing unit 30 may be further structured and disposed to accept and store the value or range of values of the predetermined change of one or more bodily functions for a plurality of users, which may be accessed by each user, for example, via a plurality of password protected storage areas, or thorough identification and verification of at least one biometric parameter of the person, as indicated above and described in more detail below.
  • the central processing unit 30, and more specifically, the data memory module 35 may be programmed with one or more preset values or range of values of the predetermined change of one or more bodily functions. Such preset values may, for example, correspond to one or more of the age, sex, weight, etc., of the person being monitored.
  • the central processing unit 30 of the present invention may be structured to detect any one of the predetermined changes described above, in at least one preferred embodiment, the central processing unit 30 is structured to detect a plurality of predetermined changes, such as, by way of example only, the predetermined changes in blood pressure, pulse rate, and temperature of the person being monitored, each of which are known to be indicative of a person experiencing the sensation of an orgasm.
  • a plurality of predetermined changes such as, by way of example only, the predetermined changes in blood pressure, pulse rate, and temperature of the person being monitored, each of which are known to be indicative of a person experiencing the sensation of an orgasm.
  • At least one preferred embodiment of the present invention further comprises an output device, as generally shown at 40, which is operatively associated with the central processing unit 30.
  • the output device 40 in one embodiment, is structured to generate an indication upon detection of a predetermined change in at least one of the preselected bodily functions by the central processing unit 30.
  • the output device 40 is structured to generate an indication upon detection of a predetermined change in each of a plurality of predetermined bodily functions being monitored during an activity monitoring period by the central processing unit 30.
  • the indication may comprise an audible alarm 42 and/or a visible alarm 44, as illustrated in Figure 5, or any other means sufficient to indicate to the person, or to any observer, that the at least one predetermined change has been detected by the central processing unit 30.
  • the output device 40 of the present invention provides the person with results which are readily understood without the assistance or interpretation of specially trained personnel .
  • the output device 40 may comprise a video display screen 46 on which a report is directly viewed directly, wherein the report may include a variety of information such as the preselected bodily function or functions being monitored, the values of the preselected bodily function comprising the baseline data set, the values of the preselected bodily function comprising the corresponding activity data set, the value or range of values for the predetermined change of the preselected bodily function, and the point in time in the activity monitoring period where the predetermined change is detected.
  • Figure 4 provides an illustration of one embodiment of such a video display screen 46. It is clear that the report displayed on the video display screen 46 could be transmitted to a printer or saved for future use in the data memory module 35 or the external data processing device via the external data transmission port 37. It is further understood that the embodiment of the present invention comprising the video display screen 46 may also comprise the audible alarm 42 and/or the visible alarm 44 described above.
  • At least one embodiment of the present invention comprises a biometric identification device, generally as shown at 50, which is disposed in a communicative relation with the central processing unit 30.
  • the biometric identification device 50 may be utilized to obtain at least one baseline biometric parameter from a person including, by way of example only, a fingerprint pattern, an iris recognition pattern, a voice and/or other sound recognition sample, and/or other patterns obtained from the person's body such as hair pattern, skin porosity, patterns, skin structure patterns, just to name a few.
  • the biometric identification device may comprise an iris scanner 52 structured to obtain a baseline iris pattern from the person during the baseline monitoring period, the baseline data set thereafter being associated and accessible only upon subsequent measuring and confirmation of a match of an active iris pattern provided by the person via the iris scanner 52.
  • the biometric identification device 50 may comprise a fingerprint scanner 54 to obtain a baseline fingerprint pattern of the person and for subsequent measurement and confirmation of the same.
  • any of the numerous other biometric parameters may be measured by a corresponding detection device and incorporated into the system of the present invention.
  • the present invention further comprises a method for detecting an uncontrollable change in a person's physiology.
  • the method includes monitoring at least one preselected bodily function of the person during a baseline monitoring period, transferring a baseline data set to a central processing unit, such as central processing unit 30 described above, and storing the baseline data set on the central processing unit.
  • the method further comprises monitoring the at least one preselected bodily function during an activity monitoring period, such as may be accomplished utilizing a sensor assembly 20 as described above.
  • the method of the present invention comprises monitoring a plurality of preselected bodily functions during the baseline monitoring period as well as during at least one activity monitoring period.
  • the present method comprises monitoring a plurality of preselected bodily functions during the baseline monitoring period and each of a plurality of different activity monitoring periods.
  • the method of the present invention further comprises transferring an activity data set corresponding to a preselected bodily function being monitored during an activity monitoring period to the central processing unit.
  • the present method comprises transferring a plurality of activity data sets, each of which corresponds to a different one of a plurality of preselected bodily functions being monitored during at least one, but preferably, during each of a plurality of different activity monitoring periods.
  • the method of the present invention comprises interpreting at least one activity data set utilizing the central processing unit, and detecting a predetermined change in the preselected bodily function between the baseline monitoring period and the activity monitoring period to which the activity data set corresponds.
  • a preferred embodiment comprises interpreting a plurality of activity data sets and detecting a predetermined change in each preselected bodily function between the baseline monitoring period and the activity monitoring period to which one of the plurality of activity data sets corresponds.
  • the method of the present invention comprises interpreting at least one but preferably a plurality of activity data sets manually, by comparing the value of each of the plurality of preselected bodily functions with one or more tables containing a value or range of values for the predetermined change for each of the plurality of preselected bodily functions.
  • the method of the present invention comprises generating an indication upon detection of the predetermined change in the at least one preselected bodily function.
  • the method comprises generating an indication upon detection of a predetermined change in each one of a plurality of preselected bodily functions being monitored during an activity monitoring period.
  • At least one embodiment of the method of the present invention further comprises obtaining at least one baseline biometric parameter from the person being monitored, for example, utilizing a biometric identification device 50, as described above.
  • the method of this embodiment includes transferring the at least one baseline biometric parameter to the central processing unit 30, and storing the baseline biometric parameter thereon.
  • This embodiment further comprises identifying the person via the biometric identification device 50 such as, for example, an iris scanner 52 or a fingerprint scanner 54, as described above, by measuring at least one active biometric parameter of the person and confirming a match with the baseline biometric parameter stored on the central processing unit 30, thereby positively identifying the person.

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Abstract

Cette invention concerne un système servant à détecter un changement incontrôlable dans la physiologie d'une personne, tel que le changement qui se produit pendant un orgasme. Ce système comprend un ensemble capteur conçu pour surveiller au moins une fonction corporelle présélectionnée pendant une période de surveillance d'activité. Cet ensemble capteur est conçu pour transférer au moins un ensemble de données d'activité correspondant à la fonction corporelle présélectionnée à destination d'une unité de traitement centrale, qui interprète l'ensemble de données d'activité et détecte un changement prédéterminé dans la fonction corporelle présélectionnée, changement qui, le cas échéant, indique une sensation particulière expérimentée par la personne. En outre, au moins une configuration de ce système comprend un dispositif de sortie conçu pour produire une indication, telle qu'une alarme sonore ou visuelle, lorsque l'unité de traitement centrale détecte un changement prédéterminé dans la fonction corporelle présélectionnée. Cette invention concerne également un procédé pour détecter un changement incontrôlable dans la physiologie d'une personne.
PCT/US2006/014911 2005-04-19 2006-04-19 Systeme et procede pour detecter un changement incontrolable dans la physiologie d'une personne WO2006113879A2 (fr)

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