A pelvic floor muscle rehabilitation training device

Abstract

This invention relates to the field of pelvic floor muscle rehabilitation technology and discloses a pelvic floor muscle rehabilitation training device, including a contact shell, an air tube fixedly connected to the outer wall of the contact shell, and an electrode probe fixedly connected to the top of the contact shell. The surface of the airbag is disinfected, and the airbag is fitted onto the outer wall of the electrode probe. The other end of the air tube is inserted into the airbag and connected to it. The electrode probe is slowly inserted into the vagina, and the device is turned on. At the same time as the electrode probe is activated, the inflation device is activated to generate gas, which enters the airbag through the air tube. As the gas continues to enter, the airbag slowly expands. When the airbag expands to a certain volume, inflation stops, and it begins to contract within a certain period of time. This allows the airbag to expand moderately after inflation, conforming to the irregular shape of the vaginal wall, ensuring stable and uniform contact between the built-in electrode and the pelvic floor muscle tissue.

Description

Technical Field

[0001] This invention relates to the field of pelvic floor muscle rehabilitation technology, specifically to a pelvic floor muscle rehabilitation training device. Background Technology

[0002] The pelvic floor muscle rehabilitation training device is based on the physiological characteristics of striated pelvic floor muscles and the neuromuscular control mechanism of the pelvic floor. Through the single or combined application of three core methods—active resistance, external stimulation, and sensory feedback—it corrects abnormal contraction patterns of the pelvic floor muscles (relaxation, spasm, compensatory contraction), improves the muscle strength, endurance, and autonomic control ability of the pelvic floor muscles, and ultimately solves pelvic floor dysfunction problems such as urinary incontinence, pelvic organ prolapse, and pelvic floor muscle pain. In some cases, during pelvic floor muscle rehabilitation training, users experience a feeling of heaviness, tightness, and dull pain due to pelvic floor muscle tension, spasm, or poor blood circulation. When using pelvic floor muscle rehabilitation instruments, the electrode probe surface cannot make full contact with the internal organs, or the position is misaligned, resulting in insufficient stimulation or excessive local stimulation, which affects the treatment effect. To address these issues, the following solutions are proposed. Summary of the Invention

[0003] To solve the above-mentioned technical problems, the present invention provides a pelvic floor muscle rehabilitation training device, including a contact shell, an air tube fixedly connected to the outer wall of the contact shell, an electrode probe fixedly connected to the top of the contact shell, and further comprising: The moving mechanism is fitted onto the outer wall of the electrode probe. The ventilation mechanism is slidably installed on the inner wall of the moving mechanism; The lifting mechanism is slidably installed on the inner wall of the moving mechanism.

[0004] Preferably, the moving mechanism includes: Force application component, which is sleeved on the outer wall of the electrode probe; The force-bearing component is fixedly installed on the inner wall of the force-applying component; Before use, the patient cleans their hands and vulva, disinfects the electrode probe and the force application component, and places the force application component on the outer wall of the electrode probe. One end of the trachea is connected to the inflation device, and the other end is inserted into the force application component and connected to it. At this time, the patient slowly inserts the electrode probe into the vagina about four centimeters, turns on the device, and at the same time the electrode probe is activated, the inflation device is activated to generate gas, which enters through the trachea, and the force application component moves accordingly.

[0005] Preferably, the ventilation mechanism includes: A rotating component is fixedly mounted on the outer wall of the force-bearing component. The braking assembly is slidably disposed on the inner wall of the force-applying assembly; When the gas is drawn in, the force-bearing component moves a certain distance, which in turn pushes the braking component to move.

[0006] Preferably, the lifting mechanism includes: The longitudinal movement component is slidably disposed on the inner wall of the force application component; A limiting component is slidably disposed on the inner wall of the force-applying component; As the gas accumulates, it causes the limiting components to move.

[0007] Preferably, the force-applying component includes an airbag sleeved on the outer wall of the electrode probe, a sealing plate slidably connected to the inner wall of the airbag, and several elastic rods fixedly connected to the outer wall of the sealing plate. When the amount of gas entering reaches a certain level, the sealing plate applies a pushing force to several elastic rods, causing a gap to be created between the sealing plate and the inner wall of the airbag, through which the gas enters.

[0008] Preferably, the force-bearing component includes a fixed plate fixedly connected to the inner wall of the airbag, a movable plate slidably connected to the inner wall of the airbag, and a ventilation plate fixedly connected to the inner wall of the airbag. In this process, the gas passing through the gap comes into contact with the surface of the movable plate and exerts a thrust on the movable plate, pushing it to the right and stopping after moving a certain distance.

[0009] Preferably, the rotating assembly includes several fixed cylinders fixedly connected to the outer wall of the vent plate, a fixed rod fixedly connected to the inner wall of the fixed cylinder, and a rotating plate rotatably connected to the outer wall of the fixed rod; The generated impact force contacts the surface of the rotating plate. The rotating plate is restricted by the protrusion on the inner wall of the fixed cylinder, making it unable to rotate. When the rotating plate loses its suction, the fixed rod is pulled by the gravity below due to its position on the upper part of the inner wall of the rotating plate, thus completing the seal.

[0010] Preferably, the braking assembly includes a sealing plate slidably connected to the inner wall of the airbag, and a rubber block is fixedly connected to the inner wall of the airbag. During the leftward movement of the movable plate, it comes into contact with the sealing plate, allowing external gas to continuously enter H, thus preventing external gas from contacting the gas inside the airbag.

[0011] Preferably, the longitudinal movement component includes a rubber rod fixedly connected to the inner wall of the airbag, a movable block fixedly connected to the bottom of the rubber rod, a contact block slidably connected to the inner wall of the airbag, and a force-bearing rod slidably connected to the inner wall of the airbag. When the movable block moves up a certain distance, it comes into contact with the contact block, triggering the sensor to remind the patient that the internal gas is about to be fully stored.

[0012] Preferably, the limiting component includes a force-applying rod slidably connected to the inner wall of the airbag, a lifting seat slidably connected to the inner wall of the airbag, a compression box slidably connected to the inner wall of the airbag, and a plurality of limiting blocks fixedly connected to the top of the compression box. As the force-bearing rod moves to the left under force, the lifting seat moves upward through the inclined plane, pushing the compression box upward. Several limit blocks move upward synchronously with the compression box, thus restricting the movable plate during the upward movement of the limit blocks.

[0013] The present invention has the following beneficial effects: (1) The present invention disinfects the surface of the airbag and puts the airbag on the outer wall of the electrode probe. The other end of the trachea is inserted into the airbag and connected to it. The electrode probe is slowly inserted into the vagina and the device is turned on. At the same time as the electrode probe is activated, the inflation device is activated to generate gas, which enters the airbag through the trachea. As the gas continues to enter, the airbag slowly expands and stops when it reaches a certain size. It then begins to contract within a certain time. Through the above components, the airbag can expand appropriately after inflation and fit the irregular shape of the vaginal wall, ensuring that the built-in electrode maintains stable and uniform contact with the pelvic floor muscle tissue.

[0014] (2) The present invention utilizes the continuous entry of the above-mentioned gas to apply a pushing force to the movable plate. When the inflation device starts to inhale, the rotating plate rotates under the suction force. Under the action of suction, the external gas passes through the rotating plate and enters the airbag. When the rotating plate loses suction, the fixed rod is located on the upper part of the inner wall of the rotating plate, so that the fixed rod is pulled by the gravity below to complete the seal. Through the above-mentioned components, the release of accumulated gas during electrical stimulation can reduce the feeling of heaviness or discomfort in the pelvic floor area and improve local circulation. If the patient has pelvic floor muscle relaxation, air is more likely to enter and stagnate when the body position changes. Since gas is a poor conductor, it may interfere with the distribution of current, resulting in uneven stimulation. Some areas are overstimulated while other areas are not effectively activated, affecting relaxation and comfort during treatment.

[0015] (3) The present invention utilizes the leftward movement of the movable plate. During the leftward movement of the movable plate, the sealing plate moves. As the sealing plate moves continuously, external gas continuously enters H. As the gas continuously enters H, it applies a pushing force to the movable block, forcing the movable block to move upward. At the same time, it applies pressure to the rubber rod, forcing the rubber rod to be compressed. When the movable block moves up a certain distance, the sensor is triggered to remind the patient that the internal gas is about to be stored up. The above components effectively prevent external gas from contacting the gas in the airbag, breaking the preset stable pressure environment inside the airbag.

[0016] (4) This invention utilizes the leftward movement of the force rod. While the force rod is subjected to force and moves to the left, the lifting seat moves upward through the inclined plane and pushes the compression box upward. Several limiting blocks move upward synchronously with the compression box. During the upward movement of several limiting blocks, some limiting blocks come into contact with the bottom of the movable plate and cannot move upward due to the pressure of the movable plate. This applies pressure to the compression box, causing its corresponding position to move downward. Other limiting blocks that do not come into contact with the bottom of the movable plate continue to move upward and restrict the movable plate. The above components effectively prevent the movable plate from moving when the gas is about to be filled, even if the sensor is not triggered or the patient does not release the gas in the H space in time. This provides a protective function. Attached Figure Description

[0017] To more clearly illustrate the technical solutions of the embodiments of the present invention, the accompanying drawings used in the description of the embodiments will be briefly introduced below. Obviously, the drawings described below are only some embodiments of the present invention. For those skilled in the art, other drawings can be obtained based on these drawings without creative effort.

[0018] Figure 1 This is a schematic diagram of the overall structure of the present invention; Figure 2 This is a schematic cross-sectional view of the overall structure of the present invention; Figure 3 This is a schematic cross-sectional view of the overall structure of the present invention; Figure 4 This is a schematic cross-sectional view of the moving mechanism of the present invention; Figure 5 This is a schematic diagram of some parts in the rotating assembly of the present invention; Figure 6 This is a schematic cross-sectional view of the rotating component of the present invention; Figure 7 This is a schematic cross-sectional view of the lifting mechanism of the present invention; Figure 8 This is a schematic cross-sectional view of the longitudinal movement component of the present invention; Figure 9 This is a cross-sectional schematic diagram of the limiting component of the present invention.

[0019] The attached diagram lists the components represented by each number as follows: In the diagram: 1. Moving mechanism; 11. Force application component; 12. Force receiving component; 13. Contact shell; 14. Air tube; 15. Electrode probe; 111. Airbag; 112. Sealing plate; 113. Elastic rod; 121. Fixed plate; 122. Movable plate; 123. Ventilation plate; 2. Ventilation mechanism; 21. Rotating component; 22. Braking component; 211. Fixed cylinder; 212. Fixed rod; 213. Rotating plate; 221. Sealing plate; 222. Rubber block; 3. Lifting mechanism; 31. Longitudinal movement component; 32. Limiting component; 311. Rubber rod; 312. Movable block; 313. Contact block; 314. Force receiving rod; 321. Force application rod; 322. Lifting seat; 323. Compression box; 324. Limiting block. Detailed Implementation

[0020] The technical solutions of the embodiments of the present invention will be clearly and completely described below with reference to the accompanying drawings. Obviously, the described embodiments are only some embodiments of the present invention, and not all embodiments. Based on the embodiments of the present invention, all other embodiments obtained by those skilled in the art without creative effort are within the scope of protection of the present invention.

[0021] Example 1, please refer to Figures 1-7 The present invention is a pelvic floor muscle rehabilitation training device, including a contact shell 13, an air tube 14 fixedly connected to the outer wall of the contact shell 13, an electrode probe 15 fixedly connected to the top of the contact shell 13, and further comprising: The moving mechanism 1 is sleeved on the outer wall of the electrode probe 15; Ventilation mechanism 2 is slidably disposed on the inner wall of the moving mechanism 1; The lifting mechanism 3 is slidably disposed on the inner wall of the moving mechanism 1.

[0022] Mobile mechanism 1 includes: Force application component 11 is sleeved on the outer wall of electrode probe 15; Force-receiving component 12 is fixedly installed on the inner wall of force-applying component 11; Before use, the patient cleans their hands and vulva, disinfects the surface of the electrode probe 15 and the force application component 11, and places the force application component 11 on the outer wall of the electrode probe 15. One end of the trachea 14 is connected to the inflation device, and the other end is inserted into the force application component 11 and connected to it. At this time, the patient slowly inserts the electrode probe 15 into the vagina about four centimeters, turns on the device, and at the same time the electrode probe 15 is activated, the inflation device is activated to generate gas, which enters the force application component 11 through the trachea 14. As the gas continues to enter, the force application component 12 moves accordingly.

[0023] The ventilation mechanism 2 includes: Rotating component 21 is fixedly installed on the outer wall of force-bearing component 12; Braking assembly 22 is slidably disposed on the inner wall of force application assembly 11; When the gas is drawn in, the force-receiving component 12 moves and drives the rotating component 21 to move. When the force-receiving component 12 moves a certain distance, it comes into contact with the braking component 22 and pushes the braking component 22 to move.

[0024] The lifting mechanism 3 includes: The longitudinal movement component 31 is slidably disposed on the inner wall of the force application component 11; Limiting component 32 is slidably disposed on the inner wall of force application component 11; When the braking component 22 moves, as the gas accumulates, the longitudinal moving component 31 is forced to move upward. During the upward movement, it comes into contact with the limiting component 32 and causes the limiting component 32 to move.

[0025] Example 2, please refer to Figures 4-9 The present invention is a pelvic floor muscle rehabilitation training device. Based on Example 1, the force application component 11 includes an airbag 111 sleeved on the outer wall of the electrode probe 15, a sealing plate 112 slidably connected to the inner wall of the airbag 111, and a plurality of elastic rods 113 fixedly connected to the outer wall of the sealing plate 112. Before use, the patient cleans their hands and vulva, disinfects the surface of the electrode probe 15 and the airbag 111, and places the airbag 111 on the outer wall of the electrode probe 15. One end of the trachea 14 is connected to the inflation device, and the other end is inserted into the airbag 111, connecting them. The patient then slowly inserts the electrode probe 15 into the vagina about 4 cm and turns on the device. At the same time as the electrode probe 15 is activated, the inflation device is activated to generate gas, which enters the airbag 111 through the trachea 14. As the gas continues to enter, the airbag 111 slowly expands, and the sealing plate 112 is subjected to increasing gas pressure. When a certain amount of gas enters, the sealing plate 112 applies a pushing force to several elastic rods 113 and compresses them, creating a gap between the sealing plate 112 and the inner wall of the airbag 111. The gas enters through the gap, and a sealing gasket is provided at the contact point between the sealing plate 112 and the airbag 111.

[0026] The force-bearing component 12 includes a fixed plate 121 fixedly connected to the inner wall of the airbag 111, a movable plate 122 slidably connected to the inner wall of the airbag 111, and a ventilation plate 123 fixedly connected to the inner wall of the airbag 111. The gas passing through the gap contacts the surface of the fixed plate 121 and passes through several air holes on the surface of the fixed plate 121. The passing gas contacts the surface of the movable plate 122 and applies a thrust to the movable plate 122, pushing the movable plate 122 to the right. After moving a certain distance, it stops. The movable plate 122 and the airbag 111 are provided with sealing gaskets.

[0027] The rotating assembly 21 includes several fixed cylinders 211 fixedly connected to the outer wall of the vent plate 123. A fixed rod 212 is fixedly connected to the inner wall of the fixed cylinder 211, and a rotating plate 213 is rotatably connected to the outer wall of the fixed rod 212. As the movable plate 122 moves to the right and comes into contact with the surface of the fixed cylinder 211, the resulting impact comes into contact with the surface of the rotating plate 213. At this time, the rotating plate 213 cannot rotate due to the restriction of the protrusion on the inner wall of the fixed cylinder 211. When the inflation device starts to inhale, the airbag 111 shrinks accordingly, and the sealing plate 112 is simultaneously pulled and moves to the left. The movable plate 122 moves along with it. The suction force generated by the movement of the movable plate 122 acts on the surface of the rotating plate 213, causing the rotating plate 213 to rotate when it is subjected to suction. Under the action of suction, the external gas passes through the rotating plate 213 and enters the airbag 111. When the rotating plate 213 loses suction, the fixed rod 212 is positioned slightly above the inner wall of the rotating plate 213, so that the fixed rod 212 is pulled by the gravity below to complete the seal. The outer wall of the rotating plate 213 contacts the inner wall of the fixed cylinder 211, and a sealing gasket is provided at the contact point between the rotating plate 213 and the inner wall of the fixed cylinder 211.

[0028] The braking assembly 22 includes a sealing plate 221 that is slidably connected to the inner wall of the airbag 111, and a rubber block 222 is fixedly connected to the inner wall of the airbag 111. During the leftward movement of the movable plate 122, it comes into contact with the sealing plate 221 and pushes the sealing plate 221 to move. The movement of the sealing plate 221 applies a pushing force to the rubber block 222, causing the rubber block 222 to be compressed. As the sealing plate 221 continues to move, external gas continuously enters H, preventing external gas from contacting the gas in the airbag. A sealing gasket is provided at the contact point between the outer wall of the sealing plate 221 and the inner wall of the airbag 111. The sealing plate 221 is initially in contact with the outer wall of the rubber block 222.

[0029] The longitudinal movement assembly 31 includes a rubber rod 311 fixedly connected to the inner wall of the airbag 111, a movable block 312 fixedly connected to the bottom of the rubber rod 311, a contact block 313 slidably connected to the inner wall of the airbag 111, and a force-bearing rod 314 slidably connected to the inner wall of the airbag 111. As gas continuously enters H, it applies a pushing force to the movable block 312, forcing it to move upwards. Simultaneously, it applies pressure to the rubber rod 311, compressing it. When the movable block 312 moves upwards a certain distance, it contacts the contact block 313 and pushes it to the right. At this point, as the contact block 313 moves, it triggers a sensor, alerting the patient that the internal gas is about to be exhausted. As the movable block 312 continues to move upwards until it contacts the force rod 314, the force rod 314 moves to the left. A sealing gasket is provided at the contact point between the side wall of the movable block 312 and the inner wall of the airbag 111.

[0030] The limiting component 32 includes a force rod 321 slidably connected to the inner wall of the airbag 111, a lifting seat 322 slidably connected to the inner wall of the airbag 111, a compression box 323 slidably connected to the inner wall of the airbag 111, and a plurality of limiting blocks 324 fixedly connected to the top of the compression box 323. During the process of the force-bearing rod 314 shifting to the left under force, it contacts the inclined surface of the force-applying rod 321 and applies a pushing force to it, causing the force-applying rod 321 to move downwards. Simultaneously, the force-applying rod 321 contacts the lifting seat 322, pushing it to the right. This causes the lifting seat 322 to continuously move upwards along the inclined surface, pushing the compression box 323 upwards. Several limiting blocks 324 move upwards synchronously with the compression box 323. During the upward movement of the limiting blocks 324, a certain... Some limiting blocks 324 are in contact with the bottom of the movable plate 122 and cannot move upward due to the pressure of the movable plate 122. They apply pressure to the compression box 323, causing its corresponding position to move downward. Other limiting blocks 324 that are not in contact with the bottom of the movable plate 122 continue to move upward and complete the restriction on the movable plate 122. The left outer wall of the force rod 314 is in contact with the top inclined surface of the force application rod 321, the bottom of the force rod 314 is in contact with the left inclined surface of the lifting seat 322, and the top of the lifting seat 322 is in contact with the bottom of the compression box 323.

[0031] One specific application of this embodiment is as follows: Before use, the patient cleans their hands and vulva, holds the contact shell 13, disinfects the surface of the electrode probe 15, and connects one end of the trachea 14 to the inflation device.

[0032] For users experiencing a feeling of heaviness, tightness, or dull pain during pelvic floor muscle rehabilitation training due to pelvic floor muscle tension, spasms, or poor blood circulation, the following procedure is implemented: While the patient disinfects the surface of the electrode probe 15, the surface of the airbag 111 is also disinfected. The airbag 111 is then fitted over the outer wall of the electrode probe 15, and the other end of the trachea 14 is inserted into the airbag 111, connecting it to the probe. The patient then holds the contact shell 13 and slowly inserts the electrode probe 15 into the vagina approximately four centimeters. The device is then activated, and simultaneously with the electrode probe 15 activation, the inflation device generates gas, which enters the airbag 111 through the trachea 14. As gas continues to enter, the airbag 111 slowly expands. The balloon expands to a certain point and then stops, and begins to contract within a certain time. These components allow the balloon to expand moderately after inflation, conforming to the irregular shape of the vaginal wall. This ensures stable and even contact between the internal electrodes and the pelvic floor muscles, facilitating more precise delivery of the current to the target muscle group. This avoids insufficient stimulation or excessive local stimulation due to misalignment, thus improving treatment effectiveness. Simultaneously, the current stimulation causes passive contraction of the pelvic floor muscles, strengthening them. The balloon's pressure and relaxation accelerate local blood flow, satisfying users who desire a more comfortable and relaxing experience while strengthening their training. This more effectively improves symptoms such as urinary incontinence and a feeling of heaviness, while also enhancing muscle strength and sexual sensitivity.

[0033] As the gas continuously enters, the sealing plate 112 experiences a gradually increasing gas pressure. When the amount of gas entering reaches a certain level, the sealing plate 112 applies a pushing force to several elastic rods 113 and compresses them, creating a gap between the sealing plate 112 and the inner wall of the airbag 111. The entering gas passes through this gap, contacts the surface of the fixed plate 121, and passes through several air holes on the surface of the fixed plate 121. The passing gas then contacts the surface of the movable plate 122 and applies a pushing force to it, causing the movable plate 122 to move to the right. After moving a certain distance, it contacts the surface of the fixed cylinder 211, and the resulting pressure contacts the surface of the rotating plate 213. At this point, the rotating plate 213 cannot rotate due to the restriction of the protrusion on the inner wall of the fixed cylinder 211. When the inflation device begins to inhale, the airbag 111 shrinks accordingly, and the sealing plate 112 is simultaneously pulled and moves to the left. The movable plate 122 follows suit, and the inhalation generated by the movement of the movable plate 122... Force acts on the surface of the rotating plate 213, causing it to rotate when subjected to suction. External gas passes through the rotating plate 213 and enters the airbag 111 under the suction. When the rotating plate 213 loses suction, the fixing rod 212, positioned slightly above the inner wall of the rotating plate 213, is pulled by gravity below to complete the seal. Through the above components, the release of accumulated gas during electrical stimulation can alleviate the feeling of heaviness or discomfort in the pelvic floor area, improve local circulation, and make the relaxed muscles more receptive to subsequent active training, thus enhancing the long-term rehabilitation effect. If the patient has pelvic floor muscle relaxation, such as postpartum or those with long-term increased abdominal pressure, the anterior and posterior vaginal walls may not be tightly closed, allowing air to enter more easily and linger when changing position. Since gas is a poor conductor, it may interfere with the distribution of current, leading to uneven stimulation, with some areas being overstimulated while others are not effectively activated. The lingering gas can cause heaviness, stuffiness, or dull pain in the pelvic floor area, affecting relaxation and comfort during treatment.

[0034] Utilizing the leftward movement of the movable plate 122, it contacts the sealing plate 221 during this movement, causing the sealing plate 221 to move. This movement of the sealing plate 221 applies a pushing force to the rubber block 222, compressing it. As the sealing plate 221 continues to move, external gas continuously enters H, applying a pushing force to the movable block 312, forcing it to move upwards. Simultaneously, pressure is applied to the rubber rod 311. This forces the rubber rod 311 to be compressed. When the movable block 312 moves up a certain distance, the movable block 312 comes into contact with the contact block 313 and pushes the contact block 313 to the right. At this time, as the contact block 313 moves, the sensor is triggered to remind the patient that the internal gas is about to be stored up. As the movable block 312 continues to move up until it comes into contact with the force rod 314, the force rod 314 is forced to move to the left. The above components effectively prevent external gas from coming into contact with the gas in the airbag and break the preset stable pressure environment inside the airbag.

[0035] Utilizing the leftward movement characteristic of the aforementioned force-bearing rod 314, while the force-bearing rod 314 is subjected to force and moves to the left, it simultaneously contacts the inclined surface of the force-applying rod 321 and applies a pushing force to the force-applying rod 321, pushing it downward. Simultaneously, the force-applying rod 321 contacts the lifting seat 322, pushing it to the right. This causes the lifting seat 322 to continuously move upward via the inclined surface, pushing the compression box 323 upward. Several limiting blocks 324 move upward synchronously with the compression box 323. 4. During the upward movement, some limiting blocks 324 come into contact with the bottom of the movable plate 122 and are unable to move upward due to the pressure of the movable plate 122. This applies pressure to the compression box 323, causing its corresponding position to move downward. Other limiting blocks 324 that do not come into contact with the bottom of the movable plate 122 continue to move upward and restrict the movable plate 122. The above components effectively prevent the movable plate 122 from moving when the gas is about to be filled, even if the sensor is not triggered or the patient does not release the gas in the H space in time. This provides a protective function.

[0036] The preferred embodiments of the present invention disclosed above are merely illustrative of the invention. These preferred embodiments do not exhaustively describe all details, nor do they limit the invention to the specific implementations described. Clearly, many modifications and variations can be made based on the content of this specification. This specification selects and specifically describes these embodiments to better explain the principles and practical applications of the invention, thereby enabling those skilled in the art to better understand and utilize the invention. The invention is limited only by the claims and their full scope and equivalents.

Claims

1. A pelvic floor muscle rehabilitation training device, comprising a contact shell (13), an air pipe (14) is fixedly connected to the outer wall of the contact shell (13), and an electrode probe (15) is fixedly connected to the top of the contact shell (13), characterized in that, Also includes: The moving mechanism (1) is sleeved on the outer wall of the electrode probe (15); Ventilation mechanism (2), which is slidably disposed on the inner wall of the moving mechanism (1); The lifting mechanism (3) is slidably disposed on the inner wall of the moving mechanism (1).

2. The pelvic floor muscle rehabilitation training device according to claim 1, characterized in that: The moving mechanism (1) includes: Force application component (11), which is sleeved on the outer wall of electrode probe (15); Force-receiving component (12), which is fixedly disposed on the inner wall of force-applying component (11); Before use, the patient cleans their hands and vulva, disinfects the surface of the electrode probe (15) and the force application component (11), and puts the force application component (11) on the outer wall of the electrode probe (15). One end of the trachea (14) is connected to the inflation device, and the other end is inserted into the inside of the force application component (11) and connected to it. When the electrode probe (15) is activated, the inflation device is activated to generate gas.

3. The pelvic floor muscle rehabilitation training device according to claim 2, characterized in that: The ventilation mechanism (2) includes: Rotating assembly (21), the rotating assembly (21) is fixedly disposed on the outer wall of the force-bearing assembly (12); Braking assembly (22) is slidably disposed on the inner wall of force application assembly (11).

4. The pelvic floor muscle rehabilitation training device according to claim 3, characterized in that: The lifting mechanism (3) includes: A longitudinal movement assembly (31) is slidably disposed on the inner wall of the force application assembly (11); A limiting component (32) is slidably disposed on the inner wall of the force-applying component (11).

5. The pelvic floor muscle rehabilitation training device according to claim 4, characterized in that: The force application component (11) includes an airbag (111) sleeved on the outer wall of the electrode probe (15), a sealing plate (112) is slidably connected to the inner wall of the airbag (111), and a plurality of elastic rods (113) are fixedly connected to the outer wall of the sealing plate (112). Among them, the contact point between the sealing plate (112) and the airbag (111) is provided with a sealing gasket. The airbag (111) is usually made of insulating medical silicone, which does not affect the electric field distribution.

6. The pelvic floor muscle rehabilitation training device according to claim 5, characterized in that: The force-bearing component (12) includes a fixed plate (121) fixedly connected to the inner wall of the airbag (111), a movable plate (122) slidably connected to the inner wall of the airbag (111), and a ventilation plate (123) fixedly connected to the inner wall of the airbag (111). Among them, the surfaces of the movable plate (122) and the airbag (111) are provided with sealing gaskets.

7. The pelvic floor muscle rehabilitation training device according to claim 6, characterized in that: The rotating assembly (21) includes several fixed cylinders (211) fixedly connected to the outer wall of the vent plate (123), a fixed rod (212) fixedly connected to the inner wall of the fixed cylinder (211), and a rotating plate (213) rotatably connected to the outer wall of the fixed rod (212). The outer wall of the rotating plate (213) contacts the inner wall of the fixed cylinder (211), and a sealing gasket is provided at the contact point between the rotating plate (213) and the inner wall of the fixed cylinder (211).

8. The pelvic floor muscle rehabilitation training device according to claim 6, characterized in that: The braking assembly (22) includes a sealing plate (221) slidably connected to the inner wall of the airbag (111), and a rubber block (222) is fixedly connected to the inner wall of the airbag (111). Among them, a sealing gasket is provided at the contact point between the outer wall of the sealing plate (221) and the inner wall of the airbag (111), and the sealing plate (221) is initially in contact with the outer wall of the rubber block (222).

9. A pelvic floor muscle rehabilitation training device according to claim 8, characterized in that: The longitudinal movement assembly (31) includes a rubber rod (311) fixedly connected to the inner wall of the airbag (111), a movable block (312) fixedly connected to the bottom of the rubber rod (311), a contact block (313) slidably connected to the inner wall of the airbag (111), and a force-bearing rod (314) slidably connected to the inner wall of the airbag (111). Among them, the contact point between the side wall of the movable block (312) and the inner wall of the airbag (111) is provided with a sealing gasket.

10. A pelvic floor muscle rehabilitation training device according to claim 8, characterized in that: The limiting component (32) includes a force-applying rod (321) slidably connected to the inner wall of the airbag (111), a lifting seat (322) slidably connected to the inner wall of the airbag (111), a compression box (323) slidably connected to the inner wall of the airbag (111), and a plurality of limiting blocks (324) fixedly connected to the top of the compression box (323). Among them, the left outer wall of the force-bearing rod (314) is in contact with the top inclined surface of the force-applying rod (321), the bottom of the force-bearing rod (314) is in contact with the left inclined surface of the lifting seat (322), and the top of the lifting seat (322) is in contact with the bottom of the compression box (323).

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