The present invention relates to a health management system and a program for use in the health management system, which are capable of taking an appropriate gas according to a physical condition of a user by taking hydrogen, oxygen, or the like, which is required based on a vital sign of the user detected by a wearable portable terminal, orally by a portable gas generator.
In recent years, the efficacy of hydrogen has attracted attention in studies on various animal diseases such as neurodegenerative diseases and acute pulmonary disorders, and human clinical studies in metabolic syndromes and diabetes mellitus, and various studies on medical applications have been actively conducted. Hydrogen is said to be effective in removing only the bad reactive oxides (=hydroxyl radicals), which are responsible for accelerating aging and causing various diseases such as arteriosclerosis and carcinoma, from the body. Since it does not adversely affect tissues and cells of the body, there are a wide range of methods for taking it into the body, such as intravenous administration, oral administration of aqueous solution, and inhalation of gas.
It is recommended to introduce hydrogen into the body to prevent aging and to promote beauty and well-being in a variety of conditions, particularly during exercise, stress, drinking, smoking, staying in ultraviolet/contaminated environments, sleeping deficiencies, long working hours, etc., when active O2 is likely to occur in the body. In particular, the Applicant has provided the results of the study focusing not only on the daily-aged effects due to hydrogen consumption but also on the immediate and short-time mental-physical effects due to gas aspiration of hydrogen, which had not been clarified in the past (see Patent Document 1).
Moreover, oxygen is used for generating energy of a cell and is an indispensable element for metabolism of the human body. Attention has been paid to activation of the cells in the body by oxygen, and studies have been made in recent years that conscious intake of oxygen into the body is effective in promotion of natural healing of disease conditions such as fatigue recovery and fracture, improvement of hematogenous disorder, beauty, stress reduction and the like. Actually, it is known that athletes use oxygen capsules for body shaping or treatment of injuries, and oxygen masks are used for patients with weakened physical strength.
In view of such circumstances, in recent years, there has been provided a gas generator such as a hydrogen which can consume hydrogen and oxygen, and the applicant has also provided a gas generator which is rechargeable, small in size and inexpensive so that the gas generator can be carried by a user and can be carried freely, and further, a gas generator which can selectively generate hydrogen and oxygen has been provided.
[Patent Document 1] WO2018/151107 of the International Publication
However, conventional hydrogen and other generators consume hydrogen and the like only by themselves, and because the user manages his/her physical condition and consumes hydrogen and the like at his/her own discretion when desired, it is not always possible to consume an appropriate amount of hydrogen and the like when required, and it is incomplete as a health-promoting tool. On the other hand, in recent years, with the development of wearable terminals, basic vital signs such as heart rate and respiration rate can be routinely measured, and it is easy to diagnose the physical condition of the user in real time.
The present invention has been made in view of the above circumstances, and it is an object of the present invention to provide a health management system and programs used in the health management system, which can ingest hydrogen, oxygen, or the like required based on a vital sign of a user by ingestion with a portable gas generator, thereby taking an appropriate gas according to the physical condition of the user.
In order to solve the above-mentioned problems, the present invention provides a healthcare system comprising:
a portable gas generator capable of suctioning a selected gas among mixed gases containing hydrogen and/or oxygen, which are produced by electrolysis of an electrolyte filled in at least an electrolysis tank provided inside, for a predetermined period of time by spontaneous respiration, wherein said mixed gas having an effect of promoting neural activity and/or circulatory activity of a living body; and
a wearable portable terminal for detecting a vital sign that is digitized by contacting and fixing a part of a body part.
According to the present invention, it is possible to take appropriate gas according to the physical condition of the user by taking hydrogen, oxygen, or the like required based on the vital signs of the user detected by the wearable portable terminal by ingestion with a portable gas generator.
Further, the program used in the healthcare system includes a detecting means for detecting the vital signs that are digitized by contacting and fixing the wearable portable terminal to a part of a human body part;
a first wireless transmitting means for wirelessly transmitting the vital signs to the outside; and
a calculating means for calculating a required gas and gas discharge amount and/or time that are set in advance in accordance with each of the vital signs detected by the wearable portable terminal, and further comprising any one of the following (1), (2) and (3).
(1) Second wireless transmission means for wirelessly transmitting the required gas discharged from the gas generator and the gas discharge amount and/or time to the outside
(2) Control signal transmitting means for transmitting a control signal based on the calculated required gas and gas discharge amount and/or time, and control means for receiving the control signal to control the power supply of the portable gas generator
(3) Second wireless transmission means for wirelessly transmitting the required gas and the gas discharge amount and/or time discharged from the gas generator to the outside, control signal transmission means for transmitting a control signal based on the calculated required gas and gas discharge amount and/or time, and control means for receiving the control signal and controlling the power supply of the portable gas generator
According to the present invention, data of a vital sign of a user detected by a wearable portable terminal is transmitted to a portable terminal such as a smart phone or a server, for example, and is analyzed by an installed analysis application (calculation means) to detect a selection of a gas necessary for the user, a necessary amount, and the like. This allows the user to ingest a gas corresponding to his/her physical condition with a portable gas generator.
In addition, the user can automatically ingest a necessary amount of gas by transmitting a control signal for operating the portable gas generator with respect to the necessary gas in real time, which is calculated by the portable communication terminal. Therefore, the user can ingest the optimum gas and manage the health without making a self-judgment.
Here, as in (1), when only the second wireless transmission means is provided, the user can manually select a gas of a desired type, amount, and time using the analysis result as an index, and ingest the gas from the portable gas generator.
As shown in (2), when only the control signal transmitting means and the control means is provided, the user automatically selects the desired type, amount, and time of the gas in the index of the analysis result, at this time, it may be manual only the start and end of the generation of the gas.
When all means of the second radio transmission means, the control signal transmission means, and the control means are provided as in (3), either automatic or manual can be adopted.
The wearable portable terminal may include the calculating means. That is, the selection and calculation of the necessary gas may be performed by the wearable portable terminal. Specifically, the wearable portable terminal includes calculation means for calculating a necessary gas and a gas discharge amount and/or time set in advance in accordance with each of the detected vital signs.
Further, the wearable portable terminal at this time transmits a control signal based on the calculated required gas and gas emission (discharge) amount and/or time, control board of the portable gas generator receives the control signal, it is also possible to control the power supply.
According to the present invention, since a portable terminal such as a smartphone or a server is unnecessary and the system can be implemented only with a wearable portable terminal and a portable gas generator, the user can select whether to perform calculation via a portable terminal such as a smartphone or a server or perform calculation in a wearable portable terminal in accordance with the situation such as the degree of satisfaction of the radio transmission situation. Therefore, it can be said that the use of the system in this case is widened.
Incidentally, the above portable gas generator as an example,
a body cover member having a battery, a control board for controlling power supply from the battery; and a pair of anode electrodes energized or blocked an anode and cathode of battery by the control board;
a water reservoir electrolysis tank detachably attached to the body cover member, the pair of anode electrodes are inserted into the interior in a mounted state;
a nozzle portion having a through hole; and
a mixing portion having a flow path for fluidly connecting nozzle portion and an end portion of the electrolysis tank and introducing atmosphere.
According to the portable gas generator of the present invention, the gas can be ingested appropriately according to the physical condition of the user by ingesting hydrogen, oxygen, or the like, which is required based on the vital signs of the user detected by the wearable portable terminal, by the portable gas generator of the present invention, and the health promotion and prevention/improvement of the symptoms of the individual user can be carried out by using the portable gas generator of the present invention.
Hereinafter, a portable gas generator used in the health care system of the present invention will be exemplified. The results of tests to verify the psychological and physiological effects of hydrogen intake will be described later. First, an overview of the configuration of the portable gas generator will be described in
The gas generator is characterized in that it comprises a partition member and opening/closing means which are the main components for separating the generated hydrogen and oxygen.
In explaining the present invention, for a simple understanding, first, the organization “excluding the partition member and the opening and closing means” will be described in detail with reference to
Further,
Hereinafter, the gas generator 100 will be described mainly with reference to the assembled and exploded view of
The main body cover 1 has a shape which is long in the side of the battery reception portion 43 and is cut in such a manner that an upper portion is inclined laterally in the side of the electrolysis tank reception portion 44. The base of battery 36 body cover 1, with the body bottom cover 6 as a closing member, opens and closes the base of battery acceptance 43, and closes the base of battery acceptance 43 with the body bottom cover 6 after inserting battery 36 from the bottom during assembly. The main body bottom cover 6 is closed by a cross recessed head screw 38. Further, the body cover 1 is provided with two control board (electronic board) 33, 42 so as to sandwich battery 36 in the longitudinal direction on both sides of battery receiving portion 43, the side control board 33 of the side surface of the body cover 1 is a main control board, the suction unit 32 (aromatic generator) and the mesh electrode 17 (electrode plate) to control the power supply from battery 36 to control board 42 of electrolysis tank 10 side for supplying power to.
A decorative laminated sheet 9 is attached to the side surface of the body cover 1 along the longitudinal side surface, and a button hole 9a through which an operation button 35 to the control substrate 33 is seen, a hole 9b for LED for light irradiation from an LED substrate 30, and a hole 9c for charging connector for connecting a connector for charging the battery 36 from an external power source are provided on the decorative laminated sheet 9 in this order from the top.
By pressing on the operation button 35 three times, a power supply signal is transmitted in the control substrate 33 to the control substrate 42, and power of the battery 36 is supplied for a predetermined time to a pair of the mesh electrodes (electrode plates) 17 through a housing 31 for substrate connector and a crimping substrate 28. When the power is supplied to the mesh electrode 17, the power supply signal is transmitted in the control substrate 33 to the LED substrate 30, and the LED substrate 30 causes the LED to emit light. As a result, the user can visually recognize that hydrogen or the oxygen-gas generating condition is established by 9b of the holes for LEDs. Incidentally, it was the condition of the power supply to the mesh electrode 17 to press the operation button 35 three times when the user moves by turning on the gas generator 100 in a pocket or the like, unintentionally button operated, it is a safety condition for avoiding that the power is supplied.
The two paired mesh electrodes 17 are arranged side by side longitudinally toward the above, respectively form positive and negative electrodes, and correspond to the electric power from the positive and negative electrodes of the battery 36. Moreover, an upper end of the mesh electrode 17 has a shape cut out diagonally so as to correspond to a boundary line between the reduced diameter portion 45 and a water storage body portion 46 of the electrolysis tank 10. A lower end of the mesh electrode 17 is raised up on a terminal substrate 28 and a rod-shaped titanium electrode 16 is coupled thereto in such a manner as to achieve an electrical connection. In order to shield the mesh substrate 17 and the terminal substrate 28 from water in a state in which the mesh electrode 17 is raised, there are provided a packing 13 (made of a resin such as silicone) which is installed on the terminal substrate 28, and an O-ring (made of a resin such as silicone, hereinafter refer also to as O-ring) which is attached to a periphery of the titanium electrode 16.
The electrolysis tank 10 is a container for storing water, the reduced diameter portion 45 and the water storage body portion 46 are integrally formed in order from below, and they are connected to each other therein fluidically. The water storage body portion 46 is opened upward so that water can be poured in and is half-closed by attaching an electrolysis tank lid 12. The electrolysis tank lid 12 passes through up and down, and is provided with a through opening 12a which receives the umbrella valve 23 and a screw cap 14. Water storage main body portion 46, the outer portion 46a forms a substantially flat side wall laterally over the lower end from the upper end as shown in
Further, diameter-reduced portion 45 is thinner than water storage main body portion 46 as described above, the upper end of the outer portion 46a of the side wall side as shown in
Furthermore, in the connecting position between the upper end of the outer portion 46a of the lower end and diameter-reduced portion 45 of the outer portion 46a of water storage main body portion 46, the water shielding plate 45d extending substantially the same inclined opening 45c and the bottom portion 46c of water storage main body portion 46 is provided. The impervious plate 45d extends over the interior of the paper surface vertical direction of the entire area of FIG. Therefore, even in the case that the aqueous solution accumulated in the electrolysis tank 10 is electrolyzed and the water storage amount is reduced, water is always accumulated approximately in the entire area of the inner portion of the diameter-reduced portion 45. Specifically, even when the water storage amount is reduced and the air layer is generated partly within the electrolysis tank 10, the diameter-reduced portion 45 is filled with water in the normal standing state and the air layer is not generated until water storage amount is reduced greatly since the diameter-reduced portion 45 is first of all thinner than the water storage main body portion 46.
Even if the water storage volume is reduced to some extent, an air layer may be generated in diameter-reduced portion 45 when the gas generator 100 is inclined or placed horizontally. However, in the case of the present electrolysis tank 10, water may be filled in diameter-reduced portion 45 even in such a case. Specifically, in the case of being inclined in the leftward direction on the page space of
An upper end edge of the mesh electrode 17 is formed by being cut out diagonally so that the electrode is soaked in water in the reduced diameter portion 45 without a gap by following the shapes of the reduced diameter portion 45 and the opening 45c. Returning to
A description will be given of the umbrella valve 23 which is installed to the through opening 12a of the electrolysis tank lid 12 in the upper end of the electrolysis tank 10 When the screw cap 14 having an opening in its above and passing through up and down is installed to the through opening 12a, a vent filter 18 is interposed between a hole in a bottom portion of the screw cap 14 and a bottom portion of the through opening 12a, and an O-ring 21 is inserted into a downward periphery of the screw cap 14. The vent filter 18 is a micro hole and has a function of preventing water/dusts while adjusting an internal pressure in the opening of the screw cap 14. Moreover, the O-ring 21 shields a space between an outer peripheral wall of the opening in the screw cap 14 and an inner peripheral wall of the penetrating opening 12a from water.
Further, in the opening of the screw cap 14 amplifier valve 23 which operates in the vertical direction (made of a material having flexibility such as silicon) is attached, nozzle 5 (described later) user sucks the suction upward negative pressure acts amplifier valve 23 is raised operation, the through hole of the bottom of the screw cap 14, the through-hole 12a of electrolysis tank lid 12 It is fluidly connected to the inside of electrolysis tank 10 through. Therefore, when nozzle 5 is sucked in, hydrogen or oxygen gas rising and stored in electrolysis tank 10 is discharged to the outside. Conversely, when the user interrupts the suction and the negative pressure does not act, the ampliler condition 23 moves downward, the through hole in the bottom of the screw cap 14 is closed, and the discharge of hydrogen or oxygen gas in electrolysis tank 10 is closed.
To the electrolysis tank lid 12 to which the screw cap 14 and the umbrella valve 20 are attached, a mixer 2 is attached from above. Mixer 2 has a tubular member 2a extending downwardly as shown in
The fixing of the mixer 2 and electrolysis tank lid 12 is made by attaching the locking buttons 3 and 4. Each of the lock buttons 3 and 4 is pinched in a back and forth direction (a vertical direction on the page space of
A description will be given of the aromatic heater portion 32 which generates the aromatic air.
First, a contact terminal 37 of the battery 36 is inserted into the upper-end opening of the battery receiving portion 43 of the body cover 1. The contact terminal 37 is formed by connecting a bottom part of a large-diameter cylinder and an upper part of a small-diameter cylinder, the bottom part is inserted into the opening in the upper end of the battery receiving portion 43, and power from the battery 36 is supplied to the aromatic heater member 32. Contact terminal 37 is fastened from above to the joint 37 by a countersunk screw 38 with a cross. The joint 38 is formed in such a manner that the bottom portion of the small-diameter cylinder is connected to an approximately large-diameter discoid upper portion, and the upper portion of the contact terminal 37 and the bottom portion of the joint 38 are fitted in a nested manner.
The aromatic heater member 32 is mounted on the upper surface of the joint 8, and is pinched by the joint 8 and the mixer 2 and is fixed to the main body cover 1 when attaching the mixer 2 mentioned above. The aromatic heater member 32 is a general-purpose device, and when power is supplied, an air with aroma is generated therein and is emitted upward. Further, the mixer 2 is provided with a tubular member 2c which extends downward in parallel to the tubular member 2a mentioned above, and an upper end of the aromatic heater portion 32 is connected to the tubular member 2c. Therefore, the aromatic air discharged from the fragrance heater section 32 passes through the cylindrical member 2c as shown by the arrows in
The nozzle 5 is structured such that the approximately large-diameter discoid member in the bottom portion is integrally connected to the tubular member in the upper portion, and the bottom portion is installed onto the opening in a top surface which is fluidly connected to the tubular member 2c of the heater portion 32 in the mixer 2. As a result, hydrogen or oxygen gas from the flow path 2b and/or aromatic air from the cylindrical member 2c are discharged from the inside of nozzle 5 to the outside of the upper end. An O-ring 22 is arranged in a connection portion between the bottom portion of the nozzle 5 and the mixer 2, and the connection portion is sealed.
Moreover, the aromatic heater member 32 controls power supply from the battery 36 by the control substrate 33. As described above, the power to the mesh electrodesubstrate 17 is supplied for the predetermined time by pressing on the button 35 attached to the body cover 1 three times. As mentioned above, the electric power to the mesh substrate 17 is supplied for a predetermined time by pushing the button 35 attached to the main body cover 1 three times. In the meanwhile, when the button is held down, the control board 33 connects the contact terminal 37 under a condition that the electric power supply signal is not transmitted to the mesh electrode 17, so that the electric power from the battery 36 is supplied to the aromatic heater portion 32 for a predetermined time.
Therefore, when the user inhales nozzle 5 by pressing the button 35 three times, hydrogen or oxygen gas is released from nozzle 5, and hydrogen or oxygen gas aspiration can be enjoyed for a predetermined period (while the LED board 30 emits light), and when the button 35 is pressed for a long time, aromatic hydrogen or oxygen gas can be enjoyed.
While embodiments of the gas generator used in the health care system of the present invention have been described above, it will be apparent that the gas generator is not limited to the embodiments described, but may be modified in design within the scope of common knowledge to those skilled in the art.
Next, referring to
As another embodiment, in
Next, each step of S10 to S70 will be further described.
In S 10, the user wears the wearable portable terminal 300. Here, the wearable portable terminal 300 is worn by directly or almost directly touching the human body of the user, thereby obtaining the vital signs of the blood pressure, the pulse, the body temperature, and the like of the user. In
In S 20, the vital signs are digitized and collected as data. The collected data includes, for example, blood pressure, pulse, body temperature, and the like, but information obtained when the wearable portable terminal 300 contacts the human body can be collected.
In S 30, vital signs are transmitted from the wearable portable terminal 300 to the portable communication terminal 310 by the external wireless transmission means. The transmission means is preferably wireless, although wired may be used if desired. In
In S 40 (or S 40′), the vital sign is analyzed (detailed later) by the calculation means 320 (not shown). The results analyzed may include abnormal values of vital signs, required gas and gas emissions and/or time appropriate for a user having the abnormal values, and the like.
The determination of whether or not the vital sign is abnormal may be performed by the wearable terminal after S20.
In S50, similarly to S30, by the external wireless transmission means, the mobile communication terminal 310 is transmitted to the wearable mobile terminal 300.
In S 50, abnormal information of the numerical value of the result of the analyzed vital sign, the necessary gas and gas discharge amount and/or time appropriate for the user, and the like are transmitted.
In S60, the analysis result is confirmed by the user on the display from the wearable portable terminal 300. The user can confirm abnormal values, health (values indicating health status), required gas and gas discharge amounts and/or time, etc.
In S 70, the user aspirates gas from the portable gas generator 330. The user performs gas suction of an appropriate gas type, discharge amount, and time based on the abnormal numerical values confirmed in S60, health (numerical values indicating a health state), required gas and gas discharge amount, and/or time, etc., thereby enabling health management suitable for the user.
In S70, the analysis result transmitted to the wearable portable terminal 300 may be transmitted to the portable gas generator 330 by the wireless transmission means, and the gas of an appropriate type, discharge amount, and time may be automatically discharged from the portable gas generator 330. Appropriate gas aspiration can be performed without the user making a self-judgment, and simpler and more precise health management is possible. In this case, it may be unnecessary to confirm the analysis result of the user in S60.
In addition, the type of gas to be sucked in S70 is not limited to hydrogen and oxygen, and a gas appropriate for healthcare can be adopted, and a plurality of gases and volatile components such as a flavor considering relaxation effects can be mixed.
Next, an example of the program of the health management system will be described with reference to
First, the wearable portable terminal 300 will be described with reference to
The wearable portable terminal 300 has generally measuring means 301, transmitting means 302, receiving means 303, display means 304, recording means 306, determining means 308, and signal generating means 309.
First, the measuring means 301 determines whether or not the user touches a predetermined part of the wearable portable terminal 300. The contact pressure to the predetermined portion is detected (S100), set and generated as the contact signal P (S110), and whether the contact signal P is larger than the predetermined value c1 is determined by the determining means 308 (hereinafter, “determination” is performed by the determining means 308; hereinafter, the description of “means” is omitted as appropriate) (S120). If P>c1, it is determined that the user is in contact. When it is determined that the user is touching, a biological reaction is detected (S130), and a biological reaction signal is generated and set (S140) by the signal generation unit 309. In the example of
Next, a signal of a set vital sign is generated (S170), recorded by recording means 306 (S180), and a vital sign signal is displayed (S190) by display means 304 and transmitted externally by transmitting means (S200). When the vital signs A and B thus set exceed the predetermined values c2.2 and c3.2 (S210), it is determined that the vital signs are abnormal, and abnormal signals are generated (S220), recorded (S230), displayed (S240), and transmitted (S250).
Next, the portable communication terminal 310 will be described with reference to
The portable communication terminal 310 generally includes a transmitting means 312, a receiving means 313, a display means 314, a recording means 316, a signal generating means 319, a registered data calling means 310a, and a calculating means 320.
First, a signal transmitted from the wearable portable terminal 300 by the receiving means 313 is received (S300), it is determined whether there is an abnormal signal (S310). When there is an abnormal signal, calculating means 320 and the registered data calling means 310a are used to calculate the type, amount, and time of the gas based on the vital sign signal (details will be described later with reference to S320 and
If there is no abnormal signal, the vital sign signal is recorded (S370) and the display is displayed (S380). Transmitting (S360,S380) destination of the vital sign signal is finally portable gas generator 330, when transmitting directly (arrow A in
Next,
Portable gas generator 330 has generally transmitting means 332, receiving means 333, control means 335, contact detecting means 335d, determining means 338, a signal generating means 339.
First, signals transmitted directly or indirectly from the portable communication terminal 310 are received by the receiving unit 332 (S400). Then, in order to determine whether there are required gas signals (S410), and if so, whether the user is ready to use the portable gas generator 330, the contact detecting means 335d detects whether there is a contact at a predetermined portion and the determining means 338 determines (S420). Although S420 is a flow similar to the determination (S100 to 120) of the contact signal in the wearable portable terminal 300, it is not shown and described. If there is a contact signal, the required gas signal received is amplified by the amplifier 335a of the control unit 335, AD converted by the AD converting unit 335b (S430). Then, by switching the charge switch to the electrodes by the switching means 335c, to release the gas and its amount and time determined based on the required gas signal (S440). In addition, a gas emission signal is generated (S450) and a required gas signal and a gas emission signal are transmitted to a wearable portable terminal 300 (S460).
When there are no signals in the determination of S410 or S420, the gas is not released.
As an explanation of the embodiment of
First, a signal is received (S500) and it is determined whether or not a required gas signal is present (S510). If there are signals, the gas, quantity, and duration required for the user are recorded (S520) and displayed (S530). Then, it is determined whether there is a gas emission signal (S540), if there is a signal, records that the gas has been released (S550), and displays it (S560).
In the absence of a signal, no recording or display is performed.
In the embodiment of
The program flow in the order of (a) to (d) of
Next, with reference to
First, information which cannot be measured and often changed by the wearable portable terminal 300 such as the user's weight and food volume, entered by the user is detected and set by the registered data calling means 310a (S600). Similarly, information which cannot be measured and generally variable by the wearable portable terminal 300 such as the user's gender, such as that input by the user is detected and set (S610). Next, it is determined whether or not a required gas calculation table correction signal (described later in
For example, as shown in
In order to explain the necessary gas calculation table correction signal and the integrated data signal, the description will be made with reference to
Unlike the portable communication terminal 310, the server 340 includes a program correction unit 340b and a data accumulating unit 340c. Further, from the portable gas generator 330, the server 340 gas emission signal (signal that emits gas) is transmitted (arrow C in
The program correction unit 340b generates and transmits the necessary gas calculation table correction signal. As shown in
In
The correction will be described schematically. For example, as shown in
The data accumulating means 340c receives information of all users and collects the information in a cloud form, and generates an integrated data signal. As shown in
As in the case of the required gas calculation table correction signal, although
In the calculation (S320) of the type, amount, and time of gas based on the vital sign signal by the calculation unit 320, it is possible to set the required gas calculation table suitable for one user according to the use of one user and the whole world, such as the required gas calculation table correction signal or the integrated data signal described above. In addition, generation (S660) of a required gas calculation table using integrated data signals is optimized and speeded up by performing deep learning by AI.
As a program flow, generally
In the case of
Although the health management system and the programs of the present invention have been described above, as another embodiment, for example, a configuration in which the external destination of the required gas signals in S360 of
Embodiments of the use of the health care system will now be described with reference to
When the user feels qualitative sensation (A) such as “something sleepy” or the like, “sleepiness or fatigue” is generally the cause (B). At this time, if the wearable portable terminal 300 of the present health management system is mounted, the abnormality of the “blood oxygen concentration” (C) corresponding to the qualitative sensation and cause can be quantitatively collected as data. Then, appropriate gas can be suctioned based on the collected data, and the abnormality of (C) is resolved, the cause (B) is removed, and the abnormality of the sensation (A) felt by the user is also resolved.
That is, the present health management system can quantitatively analyze the qualitative sensation felt by the user and appropriately deal with it, and therefore has the effect of being able to easily and accurately deal with an abnormality that the user does not sense, rather than a coping therapy that relies on the user's own sensation.
Using this health care system, it is possible to construct a “health data platform” 380 of the user by accumulating data 360 (exercise data, heart rate data, blood pressure, body temperature, calories consumed in
Various health management techniques 390 (e.g., meals, exercises, etc., hydrogen/oxygen suction in
By using this health management system, a platform for proposing various health management methods including hydrogen and oxygen suction can be constructed, and therefore, even health management by meals, exercises, and the like can be performed more easily and accurately than in the past without bothering the user by analyzing the platform data.
It is also conceivable that the portable communication terminal 310 is provided with calculation means capable of comparing and outputting the user's past vital signs with the current vital signs. The present health care system makes it possible to immediately visually recognize the change in vital signs caused by performing gas suction, and the effect of the present health care system can be realized, which also leads to an improvement in the motivation of health care.
In
In
Further, in
In the health management system shown in
While embodiments of the health care system and program of the present invention have been described above, it will be apparent that the health care system and program are not limited to the embodiments described, but may be modified in design within the general scope of those skilled in the art.
Next, the results of examining changes in neural activity and/or circulatory activity of a user when hydrogen is ingested using a gas-generator used in the present healthcare system will be described.
The following validation tests were conducted to confirm that parasympathetic nerves are dominant and fatigue is reduced by oral aspiration of hydrogen, and also to confirm the duration of time until the physiological index changes.
In a validation test using a gas-generator, hydrogen produced by a gas-generator (electrolysis-type hydrogen gas suction tool 100 described later) is generally sucked orally. Specifically, hydrogen generated by hydrogen generator device 100 is aspirated in spontaneous respiration for about 10 minutes. Since 8 cc of hydrogen is generated per minute by the electrolysis method (at the same time, 4 cc of oxygen is generated), 12 cc of mixed gas of oxygen and hydrogen is generated per minute in the amount of hydrogen generated per 11 minutes. The gas mixture is sucked under natural breathing. Normally, in spontaneous breathing, the exhaled air contains up to 0.24% (0.18% hydrogen and 0.06% O2) of the gas mixture generated by aspirating about 5 liters of air per minute in an adult.
The gas generated from the gas generator (hereinafter referred to as hydrogen generator 100) is hydrogen and oxygen, and both hydrogen concentration and the oxygen concentration increase in the mixed gas from the atmosphere, but the respective concentration increases are hydrogen 0.18% and oxygen 0.06% as described above, while the respective concentrations in the atmosphere are hydrogen 0.5×10−4% (=0.5 ppm) and oxygen about 21%. Therefore, it can be considered that the oxygen concentration in the mixed gas hardly increases, and only hydrogen concentration increases.
Twenty subjects were selected and were assigned to two groups according to age and study time (morning and afternoon) and measured by 10 subjects per day. The selected subjects were healthy women in their 20 s to 30 s and excluded the following.
(1) Patients who smoke (2) are cold (including those who feel cold in the summer), (3) are currently undergoing drug treatment for any disease, (4) have been taking drugs or applying drugs (excluding common cold, including a history of treatment for pollinosis), (5) have a history of serious disorders such as liver, kidney, heart, lung, blood, etc., (6) have hypertensive symptoms such as systolic blood pressure of 160 mmHg or diastolic blood pressure of 100 mmHg or more in the past month, (7) have donated more than 200 mL or more within three months, (8) have undergone pregnancy, lactation, or pregnancy disease, (10) have undergone surgery within the past month, (9) have had a history of severe disorders such as cutaneous disease, etc. Those who have participated in other human clinical studies, and those who have not participated in other human clinical studies for one month (12), Those who are considered inappropriate for this study by the investigator.
In addition, subjects were required to take cautionary notes at the time of participation in the study: (1) sleep adequately (about 7 hours) on the previous day; (2) do not use irritants such as curry and kimchi, or caffeine beverages such as coffee and tea on the meal before the study; (3) do not use perfume or puffeume on the day of measurement; (4) on the day of measurement, the subject can accept the cosmetic product to be removed and measured by pigmentation; and (5) on the day of the study (good before the study), the test was performed by removing glasses and contact lenses.
The testing method is as follows:
(1) In this study, subjects should aspirate hydrogen.
(2) The physiological effects of hydrogen will be verified by testing and evaluating each subject as described below while aspirating hydrogen, and comparing and examining each evaluation before and after aspiration.
(3) For subjects who are sitting in a chair for measurement and are open, the study director or the study collaborator prepares a hydrogen generator (which does not generate hydrogen) as a control, and assigns them to the subject. The subject should attach a mouth to the nozzles 5 (see
(4) The study director shall confirm that no adverse events have occurred in the subject during the study period.
In this verification test of the bioactivation method for enhancing a neural activity and/or a blood circulation activity of a living body, specifically, the following tests were conducted and evaluated:
For the analysis of the action of the autonomous nervous system, the pupil-to-light reaction measurement method and the skin temperature measurement method of the palm part (index finger) which can measure in a short time with little burden of the examinee, though it is high sensitivity, are carried out. Their measuring methods are explained below.
1-1) Pupil Reflection to Light
After fitting a goggle measuring device for measuring the pupil diameter, the pupil was accustomed to night vision (usually in night vision for 2 minutes). By short-time irradiating the pupil with a very weak red light emitting diode light for about 0.2 seconds to 1.0 seconds, the pupil was temporarily constricted by the light reflection, and the pupil expanded quickly thereafter. Accordingly, the pupil diameter changes during the pupil constriction and dilation reaction during the period before and after the state are photographed with a highly sensitive CCD camera (instrument: iriscoder, Hamamatsu Photonics), and the changes in pupil diameter, pupil constriction speed, and pupil dilation speed are analyzed to determine whether autonomous nervous activity dominates sympathetic activity, or whether parasympathetic activity dominates. When the parasympathetic activity is dominant, the parasympathetic activity becomes dominant as the pupil diameter becomes smaller when the light is sensed, and as the pupil constriction rate (CR) increases, the parasympathetic activity becomes dominant as the pupil constriction rate (CR) increases.
1-2) Fingertip Temperature
Focusing on the physiological response that the skin temperature in the peripheral region (this time, the central forehead and the ventral part of the first joint of the index finger) changes due to superiority or inferiority of sympathetic nerve activity, the change in the skin temperature before and after drinking hydrogen water will be measured with temperature sensors over time. The temperature sensor body has a thickness of about 1 mm and a diameter of about 3 mm, and changes in skin temperature are measured from the sensor to a recorder by wire.
Concerning the effect of central nervous activity by hydrogen, the activity (fatigue rate) of the brain is measured by the flicker device, while the brain stress test utilized for the purpose of evaluating the activity and stress of the brain is carried out. In addition, the effects of visual field function, skin sensation function, and center of gravity balance function, etc. are measured by the cerebral execution function meter. In addition, regarding mood emotion change, focus, sleepiness, etc. are interrogated with a multifaceted emotional state scale. The respective measurements will be described in brief below.
2-1) Brain Stress Test
Evaluate and analyze cerebral stress and cerebral turnover (activity) by sequentially touching the single-digit-single-digit (→2→per→, up to →3→ . . . → and →20) displayed on the monitor screen. This measurement is made immediately after the control and the subject sample (hydrogen) are suctioned.
2-2) Flicker Measurement
By judging the flashing frequency (flicker value) of the green LED light, whose frequency varies from 70 to 30 Hz, the activity of the brain (which can also be regarded as fatigue level) is measured. Specifically, it determines the frequency when the green feels flashing by continuously decreasing the frequency from 70 Hz. This measurement is repeated five times. This measurement is made immediately after the control and the subject sample (hydrogen) are suctioned.
2-3) Analysis (Measuring Instrument; Brain Execution Function Total, Manufactured by Anima Co., Ltd.) of the Effect on Brain Execution Function (Comprehensively Analyzing Left-Right Cognitive, Visual Field Function, Short-Term Memory, Skin Sensation, Barycentric Balance, Etc.).
Specifically, it is judged whether the white circle appearing on the personal computer is on the left or right side from the center line, and it is judged as soon as possible whether the button is pressed or whether the left or right vibration plate is vibrated, and it is judged as soon as possible that the button is pressed, and the moving distance of the center of gravity of the standing position is measured for 30 seconds on the center of gravity swing meter. This measurement is performed immediately after aspiration of the controls and test samples (hydrogen).
2-4) Multilateral Emotional State Scale
Twenty items of four subscales of “depression and anxiety,” “boredom,” “active pleasure,” and “inactive pleasure” were used. Subjective evaluation is performed immediately after aspiration of controls and test samples (hydrogen) with a five-point evaluation from “not at all sensed=0” to “clearly sensed=4”.
The aforementioned test results will be described.
The result of the pupil reflection to light in 1-1) is as in the following Table 1, and
The results of 1-2) point temperature are shown in Table 2 below. As in
The results of 2-1) brain stress test and 2-2) flicker measurements (including brain age evaluation) are shown in Table 3 below, and
The result of 2-3) Brain function measurement is as in the following Table 4, which is a result converted into an evaluation in score of a visual sense, an aural sense, finger tapping, grasping power, gravity balance, cognitive function (right-and-left cognitive function, short-term memory). The short-term memory and the right-and-left cognitive function should attract attention.
The result of 2-4) Multilateral emotional state scale is shown in
Number | Date | Country | Kind |
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2017-216613 | Nov 2017 | JP | national |
2018-198737 | Oct 2018 | JP | national |
Filing Document | Filing Date | Country | Kind |
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PCT/JP2018/041058 | 11/5/2018 | WO | 00 |