Multi-target percutaneous electrical stimulator and autism diagnosis and treatment method
By introducing transmission structures such as racks, gears, and rotating rods into the multi-target transcutaneous electrical stimulator, the problem of not being able to stop quickly in an emergency is solved, enabling rapid disconnection and safe storage of the connecting wires, thus improving the safety and ease of use of the device.
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Applications(China)
- Current Assignee / Owner
- Filing Date
- 2026-02-27
- Publication Date
- 2026-04-03
AI Technical Summary
Existing multi-target transcutaneous electrical stimulators may cause malfunctions or misoperation by parents in emergency situations, potentially damaging children's skin and causing panic.
A multi-target transcutaneous electrical stimulation device was designed. Through a transmission structure such as a rack, pinion, and rotating rod, the connecting wire can be quickly disconnected from the connection port. Combined with a fixing component and a storage component, the connecting wire is disconnected from the patient and stored safely.
It enables rapid interruption of treatment in emergency situations, avoids equipment misoperation, protects children's skin, reduces panic, and ensures the safety and ease of use of the equipment.
Smart Images

Figure CN121775321A_ABST
Abstract
Description
Technical Field
[0001] This invention relates to the field of stimulator technology, specifically to a multi-target transcutaneous electrical stimulation device and a method for diagnosing and treating autism. Background Technology
[0002] Multi-target transcutaneous electrical stimulation (MTS) is a non-invasive device that applies specific electrical pulses to multiple nerve or acupoint targets in the human body through skin electrodes for neuromodulation and rehabilitation. In the diagnosis and treatment of autism, it is often used in the form of transcutaneous electrical stimulation at acupoints (TEAS) and multi-channel transcutaneous electrical nerve stimulation (TENS), combined with behavioral training to achieve synergistic intervention. The core is the precise location of the target and personalized parameter settings.
[0003] When the equipment malfunctions, it continues to output current, causing severe skin irritation. Parents, unsure whether the machine has stopped, repeatedly press buttons or check the equipment, delaying the treatment of the child's discomfort; or they may misjudge that the machine has not stopped, leading to excessive operation, such as forcibly removing electrodes, which can damage the child's skin and exacerbate the child's panic. Summary of the Invention
[0004] To address the shortcomings of existing technologies, this invention provides a multi-target transcutaneous electrical stimulation device and a method for diagnosing and treating autism, solving the problem that parents cannot quickly stop the device in emergency situations.
[0005] To achieve the above objectives, the present invention provides the following technical solution: a multi-target transcutaneous electrical stimulation (TENS) device, comprising a stimulator, with connecting frames fixedly connected to both sides of the stimulator, a movable frame slidably connected to the outer wall of the stimulator, multiple rubber pads installed at the bottom of the stimulator, multiple connection ports installed at one end of the stimulator, connecting wires slidably connected to the outer wall of the connection ports, and a patch provided at the other end of the connecting wires, a rotating rod 1 and a rotating rod 2 rotatably connected to the inner wall of the connecting frames, a gear 1 and a worm gear fixedly connected to the outer wall of the rotating rod 1, a worm gear and a gear 2 fixedly connected to the outer wall of the rotating rod 2, a rack 1 fixedly connected to both sides of the movable frame 1, a movable frame 2 slidably connected to the inner walls of the two connecting frames, a rack 2 fixedly connected to both sides of the movable frame 2, a fixing component provided on the outer wall of the movable frame 1, and a storage component provided on the inner wall of the stimulator.
[0006] By adopting the above technical solution: through the fixing component, multiple connecting wires are fixed on the moving frame one, and the moving frame two is moved downwards, so that through the transmission components such as rack two, gear two and rotating rod two at both ends, the moving frame one drives multiple connecting wires to move outwards, so that multiple connecting wires are disengaged from multiple connection ports, so that the patch on the patient is de-energized, thereby achieving the effect of interrupting the stimulation device treatment.
[0007] Preferably, the fixing component includes a fixing frame one and a fixing frame two, the fixing frame one and the fixing frame two are slidably connected to the inner wall of the movable frame one, the fixing frame one and the fixing frame two are fixedly connected to both sides of the fixing frame one and the fixing frame two, the fixing frame one is provided with a spring one on both sides of the fixing frame one, the fixing frame two is fixedly connected to a movable block one on both sides of the movable frame one, the movable frame one is rotatably connected to a gear three on both sides of the movable frame one, the fixing block one is provided with two springs two on its outer wall, and the connecting wire has a fixing groove one on its outer wall.
[0008] Preferably, the storage component includes a storage box, two of which are slidably connected to the inner wall of the stimulator. A handle is fixedly connected to the outer wall of the storage box. Fixing grooves are provided on both sides of the storage box. Multiple moving blocks 2 and 3 are slidably connected to the inner wall of the stimulator. Two springs 3 are provided on the outer wall of the moving block 2, and spring 4 is provided on the outer wall of the moving block 3.
[0009] Preferably, multiple springs three and four are disposed on the inner wall of the stimulator, the moving block three is slidably connected to the outer wall of the moving block two, the moving block two is slidably connected to the outer wall of the storage box, and the moving block two is slidably connected to the inner wall of the fixing groove three.
[0010] Preferably, the rack is meshed with the tooth end of the gear, and the worm gear is meshed with the tooth end of the worm.
[0011] Preferably, the second gear is meshed with the tooth end of the second rack, the first movable frame is slidably connected to the inner wall of the two connecting frames, and the second movable frame is slidably connected to the top of the stimulator.
[0012] Preferably, the rack three is meshed with the tooth end of the gear three, and the fixing frame one is slidably connected to the outer wall of the fixing frame two.
[0013] Preferably, the first fixing bracket and the second fixing bracket are slidably connected to the outer wall of the connecting line, and the first fixing bracket and the second fixing bracket are slidably connected to the inner wall of the first fixing groove.
[0014] Preferably, spring one and spring two are disposed on the inner wall of movable frame one, and fixed block one is slidably connected to the outer wall of fixed frame two. Fixed grooves two are provided on both sides of fixed frame two, fixed block one is slidably connected to the inner wall of fixed groove two, and movable block one is slidably connected to the outer wall of movable frame one.
[0015] Preferably, in step S1, multiple connecting wires are connected to the stimulator through multiple connection ports and fixed by a fixing component, so that the other end of the connecting wires contacts the patient through the patch, and the stimulator is activated to stimulate the patient; in step S2, after the patient feels discomfort, he / she taps the second moving frame, which, through the transmission structure of the second rack, the second gear, and the worm gear, causes the first moving frame to drive the multiple connecting wires to disengage from the multiple connection ports through the fixing component, so that the patch on the patient is no longer powered; in step S3, after using the stimulator, the multiple connecting wires and patches are placed in the storage box and stored safely by the storage component.
[0016] This invention provides a multi-target transcutaneous electrical nerve stimulation (TENS) device and a method for diagnosing and treating autism. It has the following beneficial effects:
[0017] 1. The present invention uses a transmission structure composed of two racks, two gears, and two rotating rods to indirectly drive the movement of the first moving frame through the transmission structure. This allows the first moving frame to disengage the connecting wire from the connection port through the fixed component, thereby achieving the effect of quickly interrupting the stimulation device treatment.
[0018] 2. In this invention, the gear three meshes with the rack three, so that the fixing frame one and the fixing frame two can contact the connecting wire and the fixing groove one through the elastic force of the spring one, so that the connecting wire is fixed on the moving frame one, thereby achieving the effect of convenient fixing of the connecting wire.
[0019] 3. In this invention, the moving block three contacts the moving block two, and the spring three is set between the moving block two and the inner wall of the stimulator, so that the moving block three can control the moving block two to move up and down. When the moving block two contacts the fixing groove three, the storage box is fixed inside the stimulator, achieving the effect of conveniently storing the connecting wires and patches. Attached Figure Description
[0020] Figure 1 This is an overall perspective view of the present invention;
[0021] Figure 2 This is an overall unfolded view of the present invention;
[0022] Figure 3 This is a cross-sectional view of the invention.
[0023] Figure 4 This is a cross-sectional view of the disconnected structure of the present invention;
[0024] Figure 5 This is an exploded view of the disassembled structure of the present invention;
[0025] Figure 6 This is a cross-sectional view of the fixed structure of the present invention;
[0026] Figure 7 This is an exploded view of the fixed structure of the present invention;
[0027] Figure 8 This is a cross-sectional view of the storage structure of the present invention.
[0028] The components include: 1. Stimulator; 2. Connecting frame; 3. Moving frame one; 4. Rack one; 5. Rotating rod one; 6. Rotating rod two; 7. Gear one; 8. Worm gear; 9. Worm; 10. Gear two; 11. Moving frame two; 12. Rack two; 13. Connecting port; 14. Connecting wire; 15. Rubber pad; 16. Fixing assembly; 1601. Fixing frame one; 1602. Fixing frame two; 1603. Rack three; 1604. Gear three; 1605. Spring one; 1606. Fixing block one; 1607. Spring two; 1608. Moving block one; 17. Storage assembly; 1701. Storage box; 1702. Handle; 1703. Moving block two; 1704. Moving block three; 1705. Spring three; 1706. Spring four. Detailed Implementation
[0029] The technical solution of the present invention will now be clearly and completely described 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.
[0030] Please see the appendix Figure 1 - Appendix Figure 5 This invention provides a multi-target transcutaneous electrical nerve stimulation (TENS) device, including a stimulator 1. Connecting frames 2 are fixedly connected to both sides of the stimulator 1. A movable frame 3 is slidably connected to the outer wall of the stimulator 1. Multiple rubber pads 15 are installed at the bottom of the stimulator 1. Multiple connection ports 13 are installed at one end of the stimulator 1. Connecting wires 14 are slidably connected to the outer wall of the connection ports 13. A patch is provided at the other end of the connecting wires 14. A rotating rod 5 and a rotating rod 6 are rotatably connected to the inner wall of the connecting frame 2. A gear 7 and a worm gear 8 are fixedly connected to the outer wall of the rotating rod 5. A worm gear is fixedly connected to the outer wall of the rotating rod 6. 9 and gear 10, rack 4 is fixedly connected to both sides of the moving frame 3, moving frame 11 is slidably connected to the inner wall of the two connecting frames 2, rack 12 is fixedly connected to both sides of the moving frame 11, fixing component 16 is provided on the outer wall of the moving frame 3, storage component 17 is provided on the inner wall of the stimulator 1, rack 4 is meshed with the tooth end of gear 7, worm gear 8 is meshed with the tooth end of worm 9, gear 10 is meshed with the tooth end of rack 12, moving frame 3 is slidably connected to the inner wall of the two connecting frames 2, and moving frame 11 is slidably connected to the top of the stimulator 1.
[0031] Specifically, rack 212 meshes with gear 210, rotating rod 26 connects gear 210 and worm 9, causing rack 212 to indirectly drive worm 9 to rotate. Worm 9 meshes with worm wheel 8. Rotating rod 15 connects gear 17 and worm wheel 8. Gear 17 meshes with rack 14, causing worm 9 to indirectly drive rack 14 to move. Moving frame 21 indirectly drives moving frame 3 to move through rack 212. Moving frame 3 drives multiple connecting wires 14 to move through fixing component 16, causing connecting wires 14 to disengage from connection port 13 and disconnect from stimulator 1, thus cutting off power to the patch on the patient and achieving the effect of quickly interrupting treatment.
[0032] Please see the appendix Figure 3 - Appendix Figure 7 The fixing component 16 includes a fixing frame 1601 and a fixing frame 1602. The fixing frame 1601 and the fixing frame 1602 are slidably connected to the inner wall of the movable frame 3. A rack 3 1603 is fixedly connected to both sides of the fixing frame 1601 and the fixing frame 2 1602. A spring 1605 is provided on both sides of the fixing frame 1601. A movable block 1608 is fixedly connected to both sides of the movable frame 3. A fixing block 1606 is slidably connected to both sides of the movable frame 3. A gear 3 1604 is rotatably connected to both sides of the movable frame 3. Two springs 2 1607 are provided on the outer wall of the fixing block 1606. A fixing groove is provided on the outer wall of the connecting wire 14. 1. Rack 3 1603 is meshed with the tooth end of gear 3 1604. Fixing bracket 1 1601 is slidably connected to the outer wall of fixing bracket 2 1602. Fixing bracket 1 1601 and fixing bracket 2 1602 are slidably connected to the outer wall of connecting line 14. Fixing bracket 1 1601 and fixing bracket 2 1602 are slidably connected to the inner wall of fixing groove 1. Spring 1 1605 and spring 2 1607 are set on the inner wall of moving frame 3. Fixing block 1 1606 is slidably connected to the outer wall of fixing bracket 2 1602. Fixing groove 2 is opened on both sides of fixing bracket 2 1602. Fixing block 1 1606 is slidably connected to the inner wall of fixing groove 2. Moving block 1 1608 is slidably connected to the outer wall of moving frame 3.
[0033] Specifically, by moving the two fixing blocks 1606 outward together, the fixing blocks 1606 disengage from the fixing groove 2, and the fixing bracket 1602 is no longer fixed. The fixing bracket 1601 moves downward through the elastic force of the spring 1605, and the fixing bracket 1601 engages with the two racks 1603 through the gear 3 1604. The fixing bracket 1601 and the fixing bracket 1602 move inward together and contact the fixing groove 1 on the connecting line 14, so that the connecting line 14 is fixed between the fixing bracket 1601 and the fixing bracket 1602, thus achieving the effect of conveniently fixing the connecting line 14.
[0034] Please see the appendix Figure 1 and attached Figure 8 The storage component 17 includes a storage box 1701. Two storage boxes 1701 are slidably connected to the inner wall of the stimulator 1. A handle 1702 is fixedly connected to the outer wall of the storage box 1701. Fixed grooves 3 are provided on both sides of the storage box 1701. Multiple moving blocks 2 1703 and moving blocks 3 1704 are slidably connected to the inner wall of the stimulator 1. Two springs 3 1705 are provided on the outer wall of the moving block 2 1703. Springs 4 1706 are provided on the outer wall of the moving block 3 1704. Multiple springs 3 1705 and springs 4 1706 are provided on the inner wall of the stimulator 1. Moving block 3 1704 is slidably connected to the outer wall of moving block 2 1703. Moving block 2 1703 is slidably connected to the outer wall of the storage box 1701. Moving block 2 1703 is slidably connected to the inner wall of the fixed groove 3.
[0035] Specifically, the spring force of spring 1705 causes it to move upward and contact the storage box 1701. When the moving block 1703 contacts the fixing groove 3, the storage box 1701 is fixed inside the stimulator 1, allowing the storage box 1701 to store the connecting wire 14 and the patch. Moving the moving block 1704 causes the moving block 1703 to move downward, allowing the moving block 1703 to disengage from the fixing groove 3, so that the storage box 1701 is no longer fixed, achieving the effect of conveniently storing the connecting wire 14 and the patch.
[0036] Please see the appendix Figure 1 - Appendix Figure 8 S1. Connect multiple connecting wires 14 to the stimulator 1 through multiple connecting ports 13 and fix them with the fixing component 16, so that the other end of the connecting wires 14 contacts the patient through the patch, and start the stimulator 1 to stimulate the patient; S2. After the patient feels discomfort, he / she taps the second moving frame 11, so that the second moving frame 11, through the transmission structure such as the second rack 12, the second gear 10 and the worm gear 9, drives the first moving frame 3 through the fixing component 16 to disengage the multiple connecting wires 14 from the multiple connecting ports 13, so that the patch on the patient is no longer powered; S3. After using the stimulator 1, place the multiple connecting wires 14 and the patch in the storage box 1701 and store them safely through the storage component 17.
[0037] Specifically, by connecting one end of the connecting wire 14 to the connection port 13 on the stimulator 1, one end of the connecting wire 14 is fixed to the moving frame 3 by the fixing component 16, and the other end of the connecting wire 14 contacts the patient through the patch, so that the stimulator 1 stimulates the patient's skin through the connection port 13, the connecting wire 14 and the patch; the moving frame 2 11 is moved downward, so that it drives the connecting wire 14 to disengage from the connection port 13 through the fixing component 16 via the transmission components such as the rack 2 12, the gear 2 10 and the rotating rod 2 6, so that the moving frame 3 drives the connecting wire 14 to disengage from the connection port 13, so that the patch is de-energized; then the moving block 1 1608 is moved downward, so that it drives the fixing frame 2 1602 to move downward, so that the fixing frame 1 1601 and the fixing frame 2 1602 no longer fix the connecting wire 14, so that the connecting wire 14 and the patch are placed in the storage box 1701, and the storage box 1701 is fixed in the stimulator 1 by contacting the solid groove 3 through the moving block 2 1703.
[0038] Working principle: Press the moving block 3 1704 to compress the spring 4 1706, so that the other end of the moving block 3 1704 contacts the moving block 2 1703, causing the moving block 2 1703 to move downward and disengage from the fixing groove 3, so that the storage box 1701 is no longer fixed. Then, move the storage box 1701 by the handle 1702 to detach part of the storage box 1701 from the stimulator 1, and take out the connecting wire 14 and the patch from the storage box 1701.
[0039] One end of the connecting wire 14 is connected to the connecting port 13, and the other end of the connecting wire 14 is connected to the patch, allowing the patch to be applied to the patient's skin. Then, the fixing block 1606 is disengaged from the fixing groove 2, so that the fixing frame 1601 and the fixing frame 2 1602 are in contact with the solid groove 1 through the rack 3 1603, the gear 3 1604 and the spring 1605, so that the connecting wire 14 is fixed on the moving frame 3. When the patient feels discomfort, the moving frame 2 11 is moved downward, so that the moving frame 2 11 is driven to move the moving frame 3 outward through the transmission components such as the rack 2 12, the gear 2 10 and the rotating rod 2 6, so that the connecting wire 14 is disengaged from the connecting port 13, and the connecting wire 14 is disconnected from the stimulator 1, so that the patch on the patient's body is de-energized, achieving the effect of quickly interrupting the treatment of the stimulator 1.
[0040] Although embodiments of the invention have been shown and described, it will be understood by those skilled in the art that various changes, modifications, substitutions and alterations can be made to these embodiments without departing from the principles and spirit of the invention, the scope of which is defined by the appended claims and their equivalents.
Claims
1. A multi-target transcutaneous electrical stimulation device, comprising a stimulator (1), characterized in that: The stimulator (1) is fixedly connected to both sides by a connecting frame (2). A movable frame (3) is slidably connected to the outer wall of the stimulator (1). Multiple rubber pads (15) are installed at the bottom of the stimulator (1). Multiple connection ports (13) are installed at one end of the stimulator (1). A connecting line (14) is slidably connected to the outer wall of the connection port (13). A patch is provided at the other end of the connecting line (14). A rotating rod (5) and a rotating rod (6) are rotatably connected to the inner wall of the connecting frame (2). The rotating rod (5) 5) is fixedly connected to the outer wall of gear 1 (7) and worm gear (8), and the outer wall of the rotating rod 2 (6) is fixedly connected to worm gear (9) and gear 2 (10). Both sides of the moving frame 1 (3) are fixedly connected to rack 1 (4). The inner walls of the two connecting frames (2) are slidably connected to moving frame 2 (11). Both sides of the moving frame 2 (11) are fixedly connected to rack 2 (12). The outer wall of the moving frame 1 (3) is provided with a fixing component (16), and the inner wall of the stimulator (1) is provided with a storage component (17).
2. The multi-target transcutaneous electrical nerve stimulation device according to claim 1, characterized in that: The fixing component (16) includes a fixing frame one (1601) and a fixing frame two (1602). The fixing frame one (1601) and the fixing frame two (1602) are slidably connected to the inner wall of the movable frame one (3). The fixing frame one (1601) and the fixing frame two (1602) are fixedly connected to both sides of the fixing frame one (1601) and the fixing frame two (1602). The fixing frame one (1605) is provided on both sides of the fixing frame one (1601). The fixing frame two (1608) is fixedly connected to both sides of the fixing frame two (1602). The fixing frame one (3) is slidably connected to both sides of the fixing frame one (3). The fixing frame one (3) is rotatably connected to both sides of the fixing frame one (3). The fixing block one (1606) is provided with two springs two (1607) on the outer wall. The connecting line (14) has a fixing groove one on its outer wall.
3. The multi-target transcutaneous electrical nerve stimulation device according to claim 1, characterized in that: The storage assembly (17) includes a storage box (1701), two storage boxes (1701) are slidably connected to the inner wall of the stimulator (1), and a handle (1702) is fixedly connected to the outer wall of the storage box (1701). Fixed grooves are provided on both sides of the storage box (1701). Multiple moving blocks (2) (1703) and moving blocks (3) (1704) are slidably connected to the inner wall of the stimulator (1). Two springs (3) (1705) are provided on the outer wall of the moving block (2) (1703), and springs (4) (1706) are provided on the outer wall of the moving block (3) (1704).
4. The multi-target transcutaneous electrical nerve stimulation device according to claim 3, characterized in that: Multiple springs three (1705) and four (1706) are arranged on the inner wall of the stimulator (1). The moving block three (1704) is slidably connected to the outer wall of the moving block two (1703). The moving block two (1703) is slidably connected to the outer wall of the storage box (1701). The moving block two (1703) is slidably connected to the inner wall of the fixing groove three.
5. The multi-target transcutaneous electrical nerve stimulation device according to claim 1, characterized in that: The rack (4) is meshed with the tooth end of the gear (7), and the worm gear (8) is meshed with the tooth end of the worm (9).
6. The multi-target transcutaneous electrical nerve stimulation device according to claim 1, characterized in that: The gear two (10) is meshed with the tooth end of the rack two (12), the movable frame one (3) is slidably connected to the inner wall of the two connecting frames (2), and the movable frame two (11) is slidably connected to the top of the stimulator (1).
7. The multi-target transcutaneous electrical nerve stimulation device according to claim 2, characterized in that: The rack three (1603) is meshed with the tooth end of the gear three (1604), and the fixing frame one (1601) is slidably connected to the outer wall of the fixing frame two (1602).
8. The multi-target transcutaneous electrical nerve stimulation device according to claim 2, characterized in that: The first fixing bracket (1601) and the second fixing bracket (1602) are slidably connected to the outer wall of the connecting line (14), and the first fixing bracket (1601) and the second fixing bracket (1602) are slidably connected to the inner wall of the first fixing groove.
9. The multi-target transcutaneous electrical nerve stimulation device according to claim 2, characterized in that: The first spring (1605) and the second spring (1607) are disposed on the inner wall of the first movable frame (3). The first fixed block (1606) is slidably connected to the outer wall of the second fixed frame (1602). The second fixed frame (1602) has a second fixed groove on both sides. The first fixed block (1606) is slidably connected to the inner wall of the second fixed groove. The first movable block (1608) is slidably connected to the outer wall of the first movable frame (3).
10. A method for diagnosing and treating autism, comprising the multi-target transcutaneous electrical stimulation device according to any one of claims 1-9, characterized in that, Includes the following steps: S1. Connect multiple connecting wires (14) to the stimulator (1) through multiple connecting ports (13) and fix them through the fixing component (16) so that the other end of the connecting wires (14) contacts the patient through the patch and start the motion stimulator (1) to stimulate the patient. S2. After the patient feels discomfort, he pats the second movable frame (11), so that the second movable frame (11) can be driven by the second rack (12), the second gear (10) and the worm (9) through the transmission structure, so that the first movable frame (3) can be driven by the fixed component (16) to disconnect multiple connecting wires (14) from multiple connecting ports (13), so that the patch on the patient's body is no longer powered. S3. After using the stimulator (1), place the multiple connecting wires (14) and patches into the storage box (1701) and store them safely through the storage component (17).