Bioelectric stimulation rehabilitation instrument

Abstract

The invention discloses a bioelectrical stimulation rehabilitation instrument, which comprises an electrical stimulation plate, and is characterized in that the electrical stimulation plate comprises a contact elastic plate, a support plate, a discharge bulge and an air bag; the contact elastic plate and the supporting plate are arranged at an interval so as to define a mounting cavity; the discharge protrusions are installed on the contact elastic plate and extend in the direction away from the installation cavity, and the multiple discharge protrusions are distributed at intervals and used for being conductively connected with the human body; the air bag is mounted in the mounting cavity, and the air bag is used for pushing the contact elastic plate so as to push the discharge bulge to extrude a human body; and the air pumping device is connected with the air bag. The fitting effect of the discharge part of the electrical stimulation rehabilitation instrument and the human skin can be improved.

Description

Technical Field

[0001] This invention relates to the field of medical and nursing technology, and in particular to a bioelectric stimulation rehabilitation device. Background Technology

[0002] Bioelectric stimulation rehabilitation devices use microcurrents of specific frequencies to simulate nerve signals and stimulate target muscles or nerves. Their main functions are to induce muscle contraction, relieve pain, promote blood circulation and tissue repair, and they are commonly used in sports rehabilitation, nerve function recovery, and pain management, serving as an important auxiliary device in physical therapy.

[0003] There are many types of existing bioelectric stimulation rehabilitation devices, each designed for different parts of the body, such as those for the arms, thighs, chest, and back. However, existing bioelectric stimulation rehabilitation devices designed for the chest and back often have issues with proper adhesion between the device and the skin due to the natural curvature of the chest and back. Summary of the Invention

[0004] In order to overcome the shortcomings of the prior art, the purpose of this invention is to provide a bioelectric stimulation rehabilitation device that can improve the adhesion between the discharge point of the electrical stimulation rehabilitation device and the human skin.

[0005] The objective of this invention is achieved through the following technical solution:

[0006] A bioelectric stimulation rehabilitation device includes: an electrical stimulation plate and a pumping device;

[0007] The electrical stimulation plate includes a contact elastic plate, a support plate, discharge protrusions, and an airbag; the contact elastic plate and the support plate are spaced apart to enclose and form an installation cavity; the discharge protrusions are mounted on the contact elastic plate and extend away from the installation cavity, and there are multiple discharge protrusions, which are spaced apart and used for conductive connection to the human body; the airbag is mounted in the installation cavity and is used to push the contact elastic plate to push the discharge protrusions to compress the human body;

[0008] The air pump is connected to the airbag.

[0009] Furthermore, the bioelectric stimulation rehabilitation device also includes an electrical connection structure, which includes an electrical switch and multiple power supply clamps. The electrical switch is electrically connected to each of the power supply clamps. Each power supply clamp includes at least two unit clamps, and two unit clamps belonging to the same power supply clamp are hinged to each other. Each unit clamp has a conductive connector, and the conductive connectors of two unit clamps belonging to the same power supply clamp are arranged opposite to each other and move closer or further away from each other as the two unit clamps belonging to the same power supply clamp move closer or further away from each other. The support plate has multiple insertion holes, and each insertion hole is electrically connected to one of the discharge protrusions. Each conductive connector is pluggably connected to each insertion hole so that the electrical switch provides power to the discharge protrusion through the conductive connector.

[0010] Furthermore, the support plate has insertion grooves, the openings of which are oriented away from the contact elastic plate; multiple insertion grooves are provided, and these grooves are arranged sequentially and spaced apart along the direction of gravity to form a vertical column of insertion grooves; multiple vertical columns of insertion grooves are provided, and these columns are arranged spaced apart along a first horizontal direction; the insertion holes are located within the insertion grooves; each insertion groove has at least two insertion holes, and these at least two insertion holes are arranged spaced apart along the circumference of the insertion groove on the sidewall of the insertion groove.

[0011] Furthermore, two insertion holes are provided within the same insertion groove, and the two insertion holes are spaced apart from the sidewalls of the insertion groove on opposite sides.

[0012] Furthermore, multiple airbags are provided, and the multiple airbags are arranged sequentially at intervals along the direction of gravity to form a vertical row of airbags; multiple vertical row of airbags are provided, and the multiple vertical row of airbags are arranged at intervals along a first horizontal direction; adjacent two airbags are interconnected; a second horizontal direction is defined to extend along the wall thickness direction of the electrical stimulation plate, and a corresponding insertion groove, an airbag and a discharge protrusion are arranged sequentially along the second horizontal direction.

[0013] Furthermore, the bioelectric stimulation rehabilitation device also includes a venting tube and a venting valve, one end of the venting tube being connected to the air bag, and the other end of the venting tube being connected to the venting valve.

[0014] Furthermore, two electrical stimulation plates are provided, and the two electrical stimulation plates are arranged alternately along the second horizontal direction to form a human torso accommodating cavity.

[0015] Furthermore, the bioelectric stimulation rehabilitation device also includes a shoulder rest and a strap. The two ends of the shoulder rest are respectively connected to the two electrical stimulation plates and are used to support the two electrical stimulation plates. The two ends of the strap are respectively connected to the two electrical stimulation plates. The shoulder rest and the strap are arranged alternately along the direction of gravity.

[0016] Furthermore, at least two straps are provided on the same side of the electrical stimulation plate, and the two straps on the same side of the electrical stimulation plate are arranged sequentially at intervals along the direction of gravity.

[0017] Furthermore, the power switch is installed on the electrical stimulation plate, and the electrical stimulation plate is equipped with a mobile power supply, which is electrically connected to the power switch.

[0018] Compared with the prior art, the beneficial effects of the present invention are as follows:

[0019] 1. Multiple discharge protrusions are provided, which are installed on the contact elastic plate and extend away from the mounting cavity. The multiple discharge protrusions are distributed at intervals and are used for conductive connection to the human body. The multiple discharge protrusions can cover most of the area where the user needs electrical stimulation, thereby meeting the user's electrical stimulation needs and improving the user experience.

[0020] 2. Based on the spaced arrangement of the contact elastic plate and the support plate to form an enclosed mounting cavity, the airbag is installed in the mounting cavity. This arrangement ensures that the airbag expands within the mounting cavity during inflation, thus avoiding the problem of the airbag being squeezed out of the mounting cavity during inflation and improving the working reliability of the airbag.

[0021] 3. The electrostimulation plate includes a contact elastic plate, a support plate, discharge protrusions, and an airbag. The contact elastic plate and the support plate are spaced apart to form an installation cavity. The airbag is installed in the installation cavity and is used to push the contact elastic plate to push the discharge protrusions to compress the human body. Since the contact elastic plate is made of elastic material and is elastic, while the support plate is made of rigid material and is not elastic, the airbag will push out towards the contact elastic plate during inflation, thereby causing the discharge protrusions installed on the contact elastic plate to compress the human body, thus improving the adhesion between the discharge protrusions and the human skin. Attached Figure Description

[0022] Figure 1 This is a schematic diagram of the structure of a bioelectric stimulation rehabilitation device according to the present invention;

[0023] Figure 2 for Figure 1 A magnified view of a section at point A in the middle;

[0024] Figure 3 for Figure 1 The sectional view of the left view.

[0025] In the diagram: 1. Electrical stimulation plate; 101. Contact elastic plate; 102. Support plate; 2. Discharge protrusion; 3. Airbag; 4. Mounting cavity; 5. Pumping device; 6. Electrical connection structure; 601. Electrical switch; 602. Power supply clamp; 6021. Unit clamp; 6022. Conductive connector; 7. Plug hole; 8. Plug groove; 9. Vent pipe; 10. Vent valve; 11. Shoulder strap; 12. Strap; 13. Portable power supply. Detailed Implementation

[0026] The present invention will now be further described in conjunction with the accompanying drawings and specific embodiments. It should be noted that, without conflict, the various embodiments or technical features described below can be arbitrarily combined to form new embodiments.

[0027] It should be noted that when an element is described as being "fixed to" another element, it can be directly attached to the other element or there may be an intervening element. When an element is described as being "connected to" another element, it can be directly connected to the other element or there may be an intervening element. The terms "vertical," "horizontal," "left," "right," and similar expressions used herein are for illustrative purposes only and do not represent the only possible implementations.

[0028] Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention pertains. The terminology used herein in the description of the invention is for the purpose of describing particular embodiments only and is not intended to be limiting of the invention. The term "and / or" as used herein includes any and all combinations of one or more of the associated listed items.

[0029] See Figures 1-3 A preferred embodiment of the present invention provides a bioelectric stimulation rehabilitation device, comprising: an electrical stimulation plate 1 and an air pump device 5;

[0030] The electrical stimulation plate 1 includes a contact elastic plate 101, a support plate 102, discharge protrusions 2, and an airbag 3. The electrical stimulation plate 1 may have ventilation holes extending through its wall thickness, thus improving user comfort when worn. The contact elastic plate 101 can be made of medical-grade silicone, a soft material that does not significantly irritate the skin; alternatively, other elastic materials that do not cause harm can be used. The support plate 102 can be made of a rigid material, requiring only support capabilities. The contact elastic plate 101 and support plate 102 are spaced apart to form an installation cavity 4. Multiple discharge protrusions 2 are mounted on the contact elastic plate 101 and extend away from the installation cavity 4. These multiple discharge protrusions 2 are spaced apart and used for conductive connection to the human body. The multiple discharge protrusions 2 can cover most of the area requiring electrical stimulation, thus meeting the user's needs and improving the user experience. The airbag 3 is installed in the mounting cavity 4. This arrangement ensures that the airbag 3 expands within the mounting cavity 4 during inflation, preventing it from being squeezed out and improving its reliability. The airbag 3 is used to push against the contact elastic plate 101 to push the discharge protrusion 2 against the human body. Since the contact elastic plate 101 is made of elastic material, it is elastic, while the support plate 102 is made of rigid material and is not elastic. This causes the airbag 3 to push against the contact elastic plate 101 during inflation, thereby pushing the discharge protrusion 2 installed on the contact elastic plate 101 against the human body, thus improving the fit between the discharge protrusion 2 and the human skin. The airbag 3 can be a large airbag 3 that fills the entire mounting cavity 4, pushing the entire contact elastic plate 101 out during inflation; or multiple small airbags 3 can be placed in the mounting cavity 4, one for each discharge protrusion 2.

[0031] The air pumping device 5 is connected to the airbag 3. The air pumping device 5 can be directly installed on the electrical stimulation plate 1 for easy inflation at any time; or it can be fixed in one place, and the connection can be disconnected after the airbag 3 is fully inflated; the air pumping device 5 can be a manual air pumping device 5, which has low installation cost; or it can be an air pumping device 5 with a motor, which has a faster pumping speed than the manual air pumping device 5.

[0032] Before using this invention, the contact elastic plate 101 of the electrostimulation plate 1 is first attached and fixed to the human body. Then, the pumping device 5 is started to inflate the airbag 3, causing the airbag 3 to expand within the mounting cavity 4. Due to the limited space of the mounting cavity 4, the expansion process of the airbag 3 always occurs within the mounting cavity 4, and there will be no problem of the airbag 3 being squeezed and displaced due to over-inflation, thus sliding out of the mounting cavity 4. During the inflation process of the airbag 3, since the contact elastic plate 101 is made of elastic material while the support plate 102 is not made of elastic material, the airbag 3 pushes against the contact elastic plate 101 to undergo elastic deformation, thereby squeezing it towards the human body. This also causes the discharge protrusion 2 installed on the contact elastic plate 101 to move closer to the human body, making the discharge protrusion 2 fit the human body more tightly, thereby improving the adhesion effect between the discharge protrusion 2 and the human skin.

[0033] Multiple discharge protrusions 2 are provided, mounted on the contact elastic plate 101 and extending away from the mounting cavity 4. These protrusions are spaced apart and used for conductive connection to the human body. The multiple protrusions 2 can cover most of the area requiring electrical stimulation, thus meeting the user's needs and improving the user experience. The contact elastic plate 101 and support plate 102 are spaced apart to enclose the mounting cavity 4, in which the airbag 3 is mounted. This arrangement ensures that the airbag 3's inflation always occurs within the mounting cavity 4 due to the limited space, preventing it from being squeezed out during inflation. The problem is that the airbag 3 has improved working reliability. The electrical stimulation plate 1 includes a contact elastic plate 101, a support plate 102, a discharge protrusion 2, and an airbag 3. The contact elastic plate 101 and the support plate 102 are arranged at intervals to form an installation cavity 4. The airbag 3 is installed in the installation cavity 4. The airbag 3 is used to push the contact elastic plate 101 to push the discharge protrusion 2 to squeeze the human body. Since the contact elastic plate 101 is made of elastic material and has elasticity, while the support plate 102 is made of hard material and does not have elasticity, the airbag 3 will push out towards the contact elastic plate 101 during the inflation process, thereby driving the discharge protrusion 2 installed on the contact elastic plate 101 to squeeze the human body, thereby improving the adhesion between the discharge protrusion 2 and the human skin.

[0034] Preferably, a bioelectric stimulation rehabilitation device further includes an electrical connection structure 6, which includes an electrical switch 601 and multiple power supply clips 602. The electrical switch 601 is electrically connected to each power supply clip 602. Each power supply clip 602 includes at least two unit clips 6021, and two unit clips 6021 belonging to the same power supply clip 602 are hinged to each other. Each unit clip 6021 has a conductive connector 6022, and the conductive connectors 6022 of the two unit clips 6021 belonging to the same power supply clip 602 are arranged opposite to each other and follow the two units belonging to the same power supply clip 602. The unit clamps 6021 are close to or far from each other; the support plate 102 has multiple plug holes 7, each plug hole 7 is electrically connected to one of the discharge protrusions 2. This one-to-one arrangement of plug holes 7 and discharge protrusions 2 can provide an independent current path for each discharge protrusion 2, so that even if the circuit of one discharge protrusion 2 is damaged, the other discharge protrusions 2 can still work normally, thereby improving the working reliability of the discharge protrusions 2; each conductive plug 6022 is pluggably connected to each plug hole 7 so that the power switch 601 provides power to the discharge protrusion 2 through the conductive plug 6022. The placement of the insertion hole 7 provides a clear installation path for the conductive connector 6022 on the power supply clamp 602. When the user needs to perform electrical stimulation, they only need to hold the two unit clamps 6021 of the power supply clamp 602 and insert the conductive connector 6022 directly into the insertion hole 7 to quickly complete the installation, thereby improving work efficiency. Moreover, since the two unit clamps 6021 belonging to the same power supply clamp 602 are hinged to each other, the two hinged unit clamps 6021 provide a clamp-like mechanical action, ensuring that a tight and stable electrical connection is formed between the conductive connector 6022 and the insertion hole 7, thereby reducing the risk of the conductive connector 6022 accidentally falling off the insertion hole 7 due to accidental pulling of the wire. At the same time, the setting of the power switch 601 allows the power supply to the multiple discharge protrusions 2 to be cut off from the upstream of the circuit before the conductive connector 6022 on the power supply clamp 602 is reliably clamped to the insertion hole 7 or when the overall power needs to be cut off, thereby improving the safety during operation. As an alternative to the power supply clamp 602, a positive wire can be used to connect some of the discharge protrusions 2 in series, and a negative wire can be used to connect the remaining discharge protrusions 2 in series to supply power, which can also form an effective current loop.

[0035] Preferably, the support plate 102 has insertion grooves 8, with the openings of the insertion grooves 8 facing away from the contact elastic plate 101; multiple insertion grooves 8 are provided, and the multiple insertion grooves 8 are arranged sequentially and spaced apart along the direction of gravity to form a vertical column of insertion grooves 8; multiple vertical columns of insertion grooves 8 are provided, and the multiple vertical columns of insertion grooves 8 are arranged spaced apart along a first horizontal direction. This arrangement of multiple insertion grooves 8 spaced apart along the direction of gravity and along the first horizontal direction allows the user to intuitively observe the spatial distribution of the insertion grooves 8, thereby facilitating... The discharge protrusions 2 required for discharge are aligned to effectively prevent incorrect insertion when connecting multiple power supply clips 602, improving operational convenience. The insertion holes 7 are located within the insertion grooves 8. Compared to setting protrusions on the support plate 102, the embedded structure of placing the insertion holes 7 within the insertion grooves 8 is more aesthetically pleasing. Each insertion groove 8 has at least two insertion holes 7, which are spaced apart along the circumference of the insertion groove 8 on its sidewall. By placing the insertion holes 7 on the sidewall of the insertion groove 8, rather than at the bottom, when the conductive connector 6022 of the power supply clip 602 is inserted and clamped in the insertion hole 7, the sidewall of the insertion groove 8 can provide a certain limit to the unit clamp plate 6021. This structure can resist the pulling force of the wires from different directions, thereby preventing the power supply clip 602 from rotating or loosening due to accidental force, thus improving the long-term reliability of the electrical connection of the power supply clip 602 during the use of this invention. The plug hole 7 is provided with at least two holes. This arrangement allows the conductive connector 6022 to be inserted normally through the other plug holes 7 to provide power for subsequent power supply when one plug hole 7 is blocked by debris or other reasons. This improves the reliability of operation.

[0036] Preferably, two insertion holes 7 are provided in the same insertion groove 8, and the two insertion holes 7 are spaced apart and arranged on opposite sides of the insertion groove 8. This arrangement allows current to flow in from one insertion hole 7, pass through the discharge protrusion 2 and act on the human body, and then flow back through the other insertion hole 7, thus forming a clear and symmetrical local circuit; the relative arrangement ensures that the force on the power supply clamp 602 at the two insertion holes 7 is balanced during clamping, thereby making the contact pressure distribution more uniform and the contact resistance lower and more stable.

[0037] Preferably, multiple airbags 3 are provided, and the multiple airbags 3 are arranged sequentially and spaced apart along the direction of gravity to form a vertical airbag group; multiple vertical airbag groups are provided, and the multiple vertical airbag groups are arranged separately and spaced apart along a first horizontal direction; adjacent two airbags 3 are interconnected; a second horizontal direction is defined to extend along the wall thickness direction of the electrical stimulation plate 1, and a corresponding insertion groove 8, an airbag 3, and a discharge protrusion 2 are arranged sequentially along the second horizontal direction. This arrangement allows each airbag 3 to correspond to a single discharge protrusion 2. After the airbag 3 is inflated, the pushing action of the airbag 3 will be mainly applied to the discharge protrusion 2, rather than to the entire contact elastic plate 101, so that the discharge protrusion 2 can be more closely attached to the human body surface, thereby improving the effect of electrical stimulation on the user; and this arrangement allows the position of the discharge protrusion 2 to be inserted to be directly observed from the insertion groove 8 when the conductive plug 6022 on the power supply clip 602 is inserted into the insertion hole 7, thereby reducing the risk of misinsertion.

[0038] Preferably, a bioelectric stimulation rehabilitation device further includes a venting pipe 9 and a venting valve 10. One end of the venting pipe 9 is connected to the airbag 3, and the other end of the venting pipe 9 is connected to the venting valve 10. The venting pipe 9 is a passage connecting the airbag 3 and the external environment, and the venting valve 10 is a control switch for this passage. Before using the invention, the airbag 3 is inflated, and by closing the venting valve 10, the airbag 3 can be kept in an inflated state for a long time. This allows the discharge protrusion 2 to always fit the human body during electrical stimulation, thereby improving the effect of electrical stimulation. After the user ends the electrical stimulation, the air in the airbag 3 can be released by opening the venting valve 10, allowing the airbag 3 to return to its original shape. This makes it convenient for the user to remove the electrical stimulation plate 1 after the electrical stimulation treatment ends, and also prevents the airbag 3 from being in a tight state for a long time, which helps to delay the aging of the airbag 3 material and prevent plastic deformation. At the same time, it also makes it convenient to store the electrical stimulation plate 1. The vent valve 10 can be a plug that is manually opened or closed; or a manual vent valve with a manually controlled switch; or a solenoid valve that is electrically opened or closed, etc.

[0039] Preferably, two electrical stimulation plates 1 are provided, and the two electrical stimulation plates 1 are arranged alternately along the second horizontal direction to form a human trunk accommodating cavity. A single electrical stimulation plate 1 can only stimulate one side of the human trunk, either the front or the back, during electrical stimulation. However, two oppositely arranged electrical stimulation plates 1 can act on two symmetrical areas of the trunk simultaneously, forming a three-dimensional surrounding electric field or current path, thereby improving the therapeutic effect of electrical stimulation.

[0040] Preferably, a bioelectric stimulation rehabilitation device further includes a shoulder strap 11 and a strap 12. The two ends of the shoulder strap 11 are respectively connected to two electrical stimulation plates 1 and are used to support the two plates. When the user wears the device on their torso, the shoulder strap 11 crosses the user's shoulders, using the shoulder's skeletal structure as the main load-bearing point to bear most of the weight of the two electrical stimulation plates 1, preventing them from sagging. This allows the user to wear the device for extended periods for electrical stimulation therapy, thus improving the device's ease of use. The two ends of the strap 12 are respectively connected to the two electrical stimulation plates 1. The shoulder strap 11 and strap 12 are arranged alternately along the direction of gravity. The strap 12 generates a horizontal embracing force when the user wears the device on their torso, tightly fitting the electrical stimulation plates 1 to the torso surface, thus making it easier for the user to perform electrical stimulation therapy. Furthermore, by using the shoulder strap 11 and strap 12 together, the weight is shared by the shoulders, reducing the pressure of the strap 12 on the chest and abdomen, allowing the user to breathe more naturally and comfortably during treatment and daily activities, thereby improving the device's overall comfort.

[0041] Preferably, at least two straps 12 are provided on the same side of the electrical stimulation plate 1, and the two straps 12 on the same side of the electrical stimulation plate 1 are arranged alternately along the direction of gravity. This arrangement allows at least two straps 12 to be located at different heights. When the user wears the invention, these straps 12 form multiple parallel horizontal constraint rings on the torso that act on different planes, thereby forming multiple constraint points along the direction of gravity. This ensures that the electrical stimulation plate 1 will not loosen even when the user performs some daily activities, and that the discharge protrusion 2 always fits the human body, thus ensuring the effectiveness of use. Furthermore, by providing at least two straps 12, even if one strap 12 loosens due to accidental snagging or material fatigue, the remaining straps 12 can still provide sufficient holding force to prevent the device from suddenly falling off completely, thereby improving the safety of use. The strap 12 can be equipped with a D-ring or trapezoidal buckle structure, which allows for adjustment of the tightness of the strap 12 during use, improving the user's comfort; alternatively, a hook and loop fastener strap 12 with a Velcro structure can be selected, which can quickly fasten the strap during use.

[0042] Preferably, the power switch 601 is installed on the electrical stimulation plate 1. This arrangement allows the user to easily control the discharge protrusion 2 to start or stop discharging at any time according to their own situation during the use of the present invention, thereby improving the user's ease of use. The electrical stimulation plate 1 is equipped with a mobile power supply 13, which is electrically connected to the power switch 601. Generally speaking, existing electrical stimulators for the chest and back are separated from the power supply. Due to the limited length of the wire, it is usually inconvenient for the user to move during use. However, in the present invention, the mobile power supply 13 is set on the electrical stimulation plate 1, so the user does not need to worry about the length of the wire and can move freely during the use of the present invention, thereby improving the user's ease of use.

[0043] In the description of this specification, references to terms such as "one embodiment," "some embodiments," "example," "specific example," or "some examples," etc., indicate that a specific feature, structure, material, or characteristic described in connection with that embodiment or example is included in at least one embodiment or example of this application. Furthermore, the specific features, structures, materials, or characteristics described may be combined in any suitable manner in one or more embodiments or examples. Moreover, without contradiction, those skilled in the art can combine and integrate the different embodiments or examples described in this specification, as well as the features of those different embodiments or examples.

[0044] Furthermore, the terms "first" and "second" are used for descriptive purposes only and should not be construed as indicating or implying relative importance or implicitly specifying the number of technical features indicated. Thus, a feature defined as "first" or "second" may explicitly or implicitly include at least one of that feature. In the description of this application, "a plurality of" means two or more, unless otherwise explicitly specified.

[0045] The above description is merely a specific embodiment of this application, but the scope of protection of this application is not limited thereto. Any person skilled in the art can easily conceive of various variations or substitutions within the technical scope disclosed in this application, and these should all be included within the scope of protection of this application. Therefore, the scope of protection of this application should be determined by the scope of the claims.

Claims

1. A bioelectric stimulation rehabilitation device, characterized in that, include: An electrical stimulation plate (1) includes a contact elastic plate (101), a support plate (102), discharge protrusions (2), and an airbag (3); the contact elastic plate (101) and the support plate (102) are spaced apart to form an installation cavity (4); the discharge protrusions (2) are mounted on the contact elastic plate (101) and extend away from the installation cavity (4), and there are multiple discharge protrusions (2), which are spaced apart and used to electrically connect to the human body; the airbag (3) is mounted in the installation cavity (4), and the airbag (3) is used to push the contact elastic plate (101) to push the discharge protrusions (2) to squeeze the human body; An air pump (5) is connected to the air bag (3).

2. The bioelectric stimulation rehabilitation device according to claim 1, characterized in that, The bioelectric stimulation rehabilitation device further includes an electrical connection structure (6), which includes an electrical switch (601) and multiple power supply clips (602). The electrical switch (601) is electrically connected to each of the power supply clips (602). Each power supply clip (602) includes at least two unit clips (6021), and two unit clips (6021) belonging to the same power supply clip (602) are hinged to each other. Each unit clip (6021) has a conductive connector (6022), and two unit clips (6021) belonging to the same power supply clip (602) are hinged to each other. The conductive connectors (6022) of the unit clamps (6021) are arranged opposite each other and follow the two unit clamps (6021) belonging to the same power supply clamp (602) as they approach or move away from each other; the support plate (102) has a plurality of plug holes (7), each plug hole (7) being electrically connected to one of the discharge protrusions (2); each conductive connector (6022) is pluggably connected to each plug hole (7) so that the power switch (601) provides power to the discharge protrusion (2) through the conductive connector (6022).

3. The bioelectric stimulation rehabilitation device according to claim 2, characterized in that, The support plate (102) has a insertion groove (8), the groove of the insertion groove (8) is arranged in a direction away from the contact elastic plate (101); there are multiple insertion grooves (8), and the multiple insertion grooves (8) are arranged sequentially at intervals along the direction of gravity to form a vertical column of insertion grooves (8); there are multiple vertical columns of insertion grooves (8), and the multiple vertical columns of insertion grooves (8) are arranged at intervals along a first horizontal direction; the insertion hole (7) is located in the insertion groove (8); one insertion groove (8) has at least two insertion holes (7), and at least two insertion holes (7) are arranged at intervals along the circumference of the insertion groove (8) on the side wall of the insertion groove (8).

4. The bioelectric stimulation rehabilitation device according to claim 3, characterized in that, Two insertion holes (7) are provided in the same insertion groove (8), and the two insertion holes (7) are provided on the side walls of opposite sides of the insertion groove (8) at intervals.

5. A bioelectric stimulation rehabilitation device according to claim 4, characterized in that, The airbag (3) is provided in multiple ways, and the multiple airbags (3) are arranged sequentially and spaced apart along the direction of gravity to form a vertical row of airbags; the vertical row of airbags is provided in multiple ways, and the multiple vertical row of airbags are arranged separately and spaced apart along the first horizontal direction; two adjacent airbags (3) are interconnected; the second horizontal direction is defined to extend along the wall thickness direction of the electrical stimulation plate (1), and a corresponding insertion groove (8), an airbag (3) and a discharge protrusion (2) are arranged sequentially along the second horizontal direction.

6. The bioelectric stimulation rehabilitation device according to claim 5, characterized in that, The bioelectric stimulation rehabilitation device also includes a venting pipe (9) and a venting valve (10). One end of the venting pipe (9) is connected to the air bag (3), and the other end of the venting pipe (9) is connected to the venting valve (10).

7. A bioelectric stimulation rehabilitation device according to claim 6, characterized in that, Two electrical stimulation plates (1) are provided, and the two electrical stimulation plates (1) are arranged alternately along the second horizontal direction to form a human trunk accommodating cavity.

8. A bioelectric stimulation rehabilitation device according to claim 7, characterized in that, The bioelectric stimulation rehabilitation device further includes a shoulder pad (11) and a strap (12). The two ends of the shoulder pad (11) are respectively connected to the two electric stimulation plates (1) and are used to support the two electric stimulation plates (1). The two ends of the strap (12) are respectively connected to the two electric stimulation plates (1). The shoulder pad (11) and the strap (12) are arranged alternately along the direction of gravity.

9. A bioelectric stimulation rehabilitation device according to claim 8, characterized in that, At least two straps (12) are provided on the same side of the electrical stimulation plate (1), and the two straps (12) located on the same side of the electrical stimulation plate (1) are arranged alternately along the direction of gravity.

10. A bioelectric stimulation rehabilitation device according to claim 2, characterized in that, The power switch (601) is installed on the electrical stimulation plate (1), and the electrical stimulation plate (1) is equipped with a mobile power supply (13), which is electrically connected to the power switch (601).

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