A glove for a parkinson's patient
By designing a roll-up mechanism for gloves worn by Parkinson's patients, the problem of poor contact between the electromyography sensor and vibration module and the skin was solved, enabling signal acquisition and tremor suppression effects that are adapted to different hand sizes, thus improving the applicability and functionality of the device.
Patent Information
- Authority / Receiving Office
- CN · China
- Patent Type
- Utility models(China)
- Current Assignee / Owner
- SHENZHEN TECH UNIV
- Filing Date
- 2025-04-22
- Publication Date
- 2026-07-10
AI Technical Summary
Electromyography (EMG) sensors and vibration modules need to be in close contact with the skin to effectively collect EMG signals and suppress finger tremors. Existing gloves have a fixed size and are not suitable for hands of different sizes, resulting in insufficient applicability.
A glove designed for Parkinson's patients includes a glove body, a retaining ring, a sensor, a sleeve, a drawstring, and a winding mechanism. The winding mechanism tightens the drawstring to ensure that the glove body inside the retaining ring is in close contact with the skin, adapting to different hand sizes and ensuring that the electromyography sensor and vibration module are in close contact with the skin.
It achieves close contact between the electromyography sensor and the vibration module and the skin, improving the signal acquisition effect and the vibration suppression effect on finger tremors. It is suitable for palms of different sizes and reduces the impact of finger tremors.
Smart Images

Figure CN224474493U_ABST
Abstract
Description
Technical Field
[0001] This utility model relates to the field of industrial automation technology, and in particular to a glove for Parkinson's patients. Background Technology
[0002] Parkinson's disease is a common neurodegenerative disease characterized by the gradual loss of dopaminergic neurons in the brain, leading to motor dysfunction and a range of non-motor symptoms. The 2020 "Chinese Guidelines for the Treatment of Parkinson's Disease (Fourth Edition)" clearly states that the number of Parkinson's patients in my country will rise from 1.99 million in 2005 to 5 million in 2030, accounting for almost half of the global Parkinson's disease population. Clinical diagnosis of Parkinson's disease often relies on assessment scales such as the MDS-UPDRS (Movement Disorder Society-Unified Parkinson's Disease Rating Scale) to quantify the severity of symptoms. This scale consists of four subscales, with the third subscale, motor function assessment, often susceptible to influence from physician subjectivity and patient emotions, posing challenges to diagnosis and assessment of rehabilitation outcomes.
[0003] Parkinson's disease patients often experience hand symptoms such as tremor (including resting tremor and pill-rolling tremor), rigidity, and bradykinesia. Smart wearable devices are currently the mainstream auxiliary diagnostic equipment, commonly including inertial sensing devices (gyroscopes, etc.), fingertip pressure sensors, or single-core fiber Bragg gratings to capture finger flexion. However, these devices all have significant limitations. For example, Chinese patent CN202311543974 discloses an invention entitled "Intelligent Screening and Assessment System for Parkinson's Disease Based on Multi-Data Driven Technology," whose sensors integrate accelerometers, pressure sensors, and electromyography sensors; currently, application number 2017212... Chinese utility model patent 01427.3 discloses a defibrillation smart glove. This defibrillation smart glove applies a reverse vibration force to the wearer's fingers, which is opposite to the direction of finger tremor. This can suppress finger tremor to a certain extent, reduce the amplitude of finger tremor, and alleviate the inconvenience caused by finger tremor to the wearer's daily life. However, the electromyography sensor and the vibration module need to be in close contact with the skin to better collect electromyography signals and achieve the effect of the vibration module in suppressing finger tremor and reducing the amplitude of finger tremor. The existing glove body is of a fixed size and is not suitable for different sizes of hands, so its applicability is not strong enough. Utility Model Content
[0004] The technical problem this invention aims to solve is that both the electromyography (EMG) sensor and the vibration module need to be in close contact with the skin to better collect EMG signals and effectively suppress finger tremors and reduce the amplitude of finger vibrations. However, the existing gloves are of a fixed size and are not suitable for different hand sizes, thus lacking strong applicability.
[0005] To solve the above-mentioned technical problems, the present invention provides the following technical solution: a glove for Parkinson's patients, comprising a glove body, a fixing ring, a sensor, a sleeve, a pull cord, and a winding mechanism. The fixing ring is fixedly connected to the finger area of the glove body, the sensor is fixedly connected to the glove body inside the fixing ring, one end of the pull cord is connected to the fixing ring, the pull cord passes through the sleeve and is fixedly connected to the winding mechanism, and the glove body is fixedly connected to the outer wall of the sleeve.
[0006] The winding mechanism is used to wind up the pull rope.
[0007] As a preferred embodiment of the gloves for Parkinson's patients described in this utility model, the fixing ring has an annular groove, the inner wall of the annular groove is fixedly connected to a fixing block, the fixing block is fixedly connected to one end of a pull rope, and the pull rope passes through a through hole and a sleeve.
[0008] As a preferred embodiment of the gloves for Parkinson's patients described in this utility model, the winding mechanism includes a housing, a first rotating shaft, a second rotating shaft, a first gear, a second gear, and winding drums. The outer wall of the housing is fixedly connected to the wrist position of the glove body. The two ends of the first rotating shaft and the second rotating shaft are rotatably connected to the inner wall of the housing, and multiple winding drums are respectively provided on the first rotating shaft and the second rotating shaft. The first rotating shaft is fixedly connected to the first gear, the first gear meshes with the second gear, and the second gear is fixedly connected to the second rotating shaft.
[0009] As a preferred embodiment of the gloves for Parkinson's patients described in this utility model, wherein: a first receiving cavity is provided on the first rotating shaft and the second rotating shaft respectively, one end of a first spring is fixedly connected to the bottom wall of the first receiving cavity, the other end of the first spring is fixedly connected to a movable plate, the movable plate is fixedly connected to one side of the clamping plate, and an internal gear is provided on the inner wall of the winding drum, the internal gear meshing with the other side of the clamping plate.
[0010] As a preferred embodiment of the Parkinson's disease patient wear gloves of this utility model, wherein: the first gear meshes with the third gear, the third gear is fixedly connected to the micro motor, and the micro motor is fixedly connected to the inner wall of the housing.
[0011] As a preferred embodiment of the gloves for Parkinson's patients described in this utility model, wherein: the outer wall of the fixing ring is fixedly connected to a locking mechanism, and the locking mechanism is used to lock the pull cord.
[0012] As a preferred embodiment of the gloves for Parkinson's patients described in this utility model, the locking mechanism includes a base and a cover plate, the base is hinged to the cover plate, a first guide groove is provided on the base, and a second guide groove is provided on the cover plate.
[0013] As a preferred embodiment of the gloves for Parkinson's patients described in this utility model, wherein: the inner walls of the first guide groove and the second guide groove are respectively fixedly connected with conical teeth, and multiple conical teeth are provided.
[0014] As a preferred embodiment of the Parkinson's disease patient wearing gloves of this utility model, the base is provided with a slot, the cover plate is provided with a second receiving cavity, the inner wall of the second receiving cavity is slidably connected to two sliders, the two sliders are respectively fixedly connected to the two ends of a second spring, one end of a slider is fixedly connected to a limiting rod, the limiting rod slides through the cover plate, and the other end of the limiting rod is slidably connected to the slot.
[0015] As a preferred embodiment of the gloves for Parkinson's patients described in this utility model, the slider is fixedly connected to the actuating block, and the actuating block is slidably connected to the inner wall of the limiting groove opened on the cover plate.
[0016] The beneficial effects of this utility model are as follows: This utility model can tighten the pull cord during operation through the winding mechanism. By tightening the glove body inside the fixing ring, the electromyography sensor and vibration module are in close contact with the skin, regardless of the size of the palm. It is suitable for palms of different sizes, thereby better collecting electromyography signals. The vibration module is in close contact with the skin, giving full play to the effect of vibration, thereby suppressing finger tremors, reducing the amplitude of finger tremors, and alleviating the inconvenience caused by finger tremors to the wearer's daily life. Attached Figure Description
[0017] Figure 1 This is a schematic diagram of the overall structure in an embodiment of this disclosure.
[0018] Figure 2 This is a schematic diagram of the fixed ring structure in an embodiment of this disclosure.
[0019] Figure 3 This is a cross-sectional view of the fixing ring in an embodiment of this disclosure.
[0020] Figure 4 This is a cross-sectional view of the housing in an embodiment of this disclosure.
[0021] Figure 5 This is a cross-sectional view of the winding drum in an embodiment of this disclosure.
[0022] Figure 6 For the embodiments of this disclosure Figure 5 Enlarged schematic diagram in the middle.
[0023] Figure 7This is a schematic diagram of the base structure in an embodiment of this disclosure.
[0024] Figure 8 This is a schematic diagram of the cover plate structure in an embodiment of this disclosure.
[0025] Figure 9 This is a cross-sectional view of the cover plate in an embodiment of this disclosure.
[0026] Reference numerals: 1. Glove body; 2. Fixing ring; 21. Annular groove; 22. Fixing block; 23. Through hole; 3. Sensor; 4. Sleeve; 5. Pull cord; 6. Winding mechanism; 61. Housing; 62. First rotating shaft; 63. Second rotating shaft; 64. First gear; 65. Second gear; 66. Winding drum; 631. First receiving cavity; 632. First spring; 633. Movable plate; 634. Locking plate; 67. Third gear; 7. Locking mechanism; 71. Base; 72. Cover plate; 711. First guide groove; 712. Locking groove; 721. Bevel tooth; 73. Second receiving cavity; 722. Two sliders; 723. Second spring; 724. Limiting rod; 725. Limiting groove; 726. Actuating block; 74. Detailed Implementation
[0027] To make the above-mentioned objectives, features and advantages of this utility model more apparent and understandable, the specific embodiments of this utility model will be described in detail below with reference to the accompanying drawings.
[0028] Example 1, referring to Figure 1 and Figure 2 This embodiment provides a glove for Parkinson's patients, including a glove body 1, a fixing ring 2, a sensor 3, a sleeve 4, a pull cord 5, and a winding mechanism 6. The finger area of the glove body 1 is fixedly connected to the fixing ring 2. The sensor 3 is fixedly connected to the glove body 1 inside the fixing ring 2. One end of the pull cord 5 is connected to the fixing ring 2. The pull cord 5 passes through the sleeve 4 and is fixedly connected to the winding mechanism 6. The outer wall of the sleeve 4 is fixedly connected to the glove body 1.
[0029] The winding mechanism 6 is used to wind up the pull rope 5.
[0030] In this preferred embodiment, a sensor 3 is fixedly connected inside the glove body 1 on the inner side of the fixing ring 2. The sensor 3 includes one or more of an accelerometer, a pressure sensor, and an electromyography (EMG) sensor. A vibration module is also fixedly installed inside the fixing ring 2. The vibration module applies a reverse vibration force to the wearer's fingers, opposite to the direction of finger tremor, thereby suppressing finger tremor to a certain extent, reducing the amplitude of finger tremors, and alleviating the inconvenience caused by finger tremors in the wearer's daily life. One fixing ring 2 is provided on each finger joint. The winding mechanism 6 tightens the pull cord 5 during operation. The pull cord 5 tightens the glove body 1 inside the fixing ring 2, ensuring close contact between the EMG sensor and the vibration module with the skin, regardless of hand size. This allows for better acquisition of EMG signals, and the close contact between the vibration module and the skin fully utilizes the vibration effect, thereby suppressing finger tremor, reducing the amplitude of finger tremors, and alleviating the inconvenience caused by finger tremors in the wearer's daily life.
[0031] Example 2, refer to Figures 1-9 This embodiment is based on the previous embodiment, but differs from the previous embodiment in that...
[0032] Reference Figure 3 The fixed ring 2 has an annular groove 21 inside, and a fixed block 22 is fixedly connected to the inner wall of the annular groove 21. One end of the pull rope 5 is fixedly connected to the fixed block 22, and the pull rope 5 passes through the through hole 23 and the sleeve 4.
[0033] In this preferred embodiment, the sleeve 4 protects the pull rope 5, preventing it from being exposed and from tangling together. The fixing ring 2 is made of flexible plastic or rubber, and the pull rope 5 is wrapped around the inner wall of the annular groove 21. When the pull rope 5 is pulled, the glove body 1 inside the fixing ring 2 is tightened, so that the electromyography sensor and the vibration module are in close contact with the skin.
[0034] Reference Figure 4 The winding mechanism 6 includes a housing 61, a first rotating shaft 62, a second rotating shaft 63, a first gear 64, a second gear 65, and a winding drum 66. The outer wall of the housing 61 is fixedly connected to the wrist position of the glove body 1. The two ends of the first rotating shaft 62 and the second rotating shaft 63 are respectively rotatably connected to the inner wall of the housing 61. Multiple winding drums 66 are respectively provided on the first rotating shaft 62 and the second rotating shaft 63. The first rotating shaft 62 is fixedly connected to the first gear 64, the first gear 64 meshes with the second gear 65, and the second gear 65 is fixedly connected to the second rotating shaft 63.
[0035] In this preferred embodiment, when the first rotating shaft 62 rotates, it can drive the first gear 64 to rotate, the first gear 64 can drive the second gear 65 to rotate, the second gear 65 can drive the second rotating shaft 63 to rotate, the first rotating shaft 62 and the second rotating shaft 63 can rotate on the inner wall of the housing 61, the first rotating shaft 62 and the second rotating shaft 63 drive the winding drum 66 to rotate, the other end of the pull rope 5 is fixedly connected to the winding drum 66, the rotation of the winding drum 66 winds the pull rope 5 onto the winding drum 66, tightening the pull rope 5, the pull rope 5 tightens the glove body 1 inside the fixing ring 2, so that the electromyography sensor and the vibration module are in close contact with the skin.
[0036] Reference Figure 5 and Figure 6 The first rotating shaft 62 and the second rotating shaft 63 are respectively provided with a first receiving cavity 631. The bottom wall of the first receiving cavity 631 is fixedly connected to one end of the first spring 632, and the other end of the first spring 632 is fixedly connected to the movable plate 633. The movable plate 633 is fixedly connected to one side of the clamping plate 634. The inner wall of the winding drum 66 is provided with an internal gear 661, which meshes with the other side of the clamping plate 634.
[0037] In this preferred embodiment, when the first rotating shaft 62 and the second rotating shaft 63 rotate, and the pull rope 5 is tightened, the winding drum 66 cannot rotate. However, due to the inclined surface on the internal gear 661, the inclined surface will overcome the elastic force of the first spring 632 and squeeze the clamping plate 634 and the movable plate 633. At this time, the first rotating shaft 62 and the second rotating shaft 63 rotate, but cannot drive the winding drum 66 to rotate, thus preventing the pull rope 5 from being wound too tightly and cutting the fingers.
[0038] Reference Figure 4 The first gear 64 meshes with the third gear 67, the third gear 67 is fixedly connected to the micro motor 68, and the micro motor 68 is fixedly connected to the inner wall of the housing 61.
[0039] In this preferred embodiment, when the micro motor 68 is working, it can drive the third gear 67 to rotate, the third gear 67 drives the first gear 64 to rotate, the first gear 64 can drive the first rotating shaft 62 and the second gear 65 to rotate, the second gear 65 can drive the second rotating shaft 63 to rotate, the first rotating shaft 62 and the second rotating shaft 63 can rotate on the inner wall of the housing 61, the first rotating shaft 62 and the second rotating shaft 63 drive the winding drum 66 to rotate, the other end of the pull rope 5 is fixedly connected to the winding drum 66, the rotation of the winding drum 66 winds the pull rope 5 onto the winding drum 66, tightening the pull rope 5, the pull rope 5 tightens the glove body 1 inside the fixing ring 2, so that the electromyography sensor and the vibration module are in close contact with the skin.
[0040] Reference Figure 7 The outer wall of the fixed ring 2 is fixedly connected to the locking mechanism 7, which is used to lock the pull rope 5.
[0041] The locking mechanism 7 includes a base 71 and a cover plate 72. The base 71 is hinged to the cover plate 72. A first guide groove 711 is provided on the base 71, and a second guide groove 721 is provided on the cover plate 72.
[0042] In this preferred embodiment, after the cover plate 72 is closed, the first guide groove 711 and the second guide groove 721 squeeze the pull rope 5 to position the pull rope 5, preventing the pull rope 5 in the fixing ring 2 from becoming loose, which would result in the electromyography sensor and vibration module not making close contact with the skin.
[0043] Reference Figure 7 The inner walls of the first guide groove 711 and the second guide groove 721 are respectively fixedly connected to the conical teeth 73, and multiple conical teeth 73 are provided.
[0044] In this preferred embodiment, after the cover plate 72 is closed, the conical teeth 73 in the first guide groove 711 and the second guide groove 721 squeeze the pull rope 5, further positioning the pull rope 5 and locking the pull rope 5 to prevent the pull rope 5 in the fixing ring 2 from loosening, which would result in the electromyography sensor and vibration module not making close contact with the skin.
[0045] Reference Figure 8 and Figure 9 The base 71 has a slot 712, and the cover plate 72 has a second receiving cavity 722. Two sliders 723 are slidably connected to the inner wall of the second receiving cavity 722. The two sliders 723 are respectively fixedly connected to the two ends of the second spring 724. One end of the slider 723 is fixedly connected to the limiting rod 725. The limiting rod 725 slides through the cover plate 72, and the other end of the limiting rod 725 is slidably connected to the slot 712.
[0046] In this preferred embodiment, the slider 723 is moved by the elastic force of the second spring 724. The slider 723 drives the limiting rod 725 to move. After the limiting rod 725 is inserted into the slot 712, it can lock the positions of the base 71 and the cover plate 72. At this time, the cover plate 72 cannot be opened. The conical teeth 73 in the first guide groove 711 and the second guide groove 721 squeeze the pull rope 5, further positioning the pull rope 5 and locking it to prevent the pull rope 5 in the fixing ring 2 from loosening, which would cause the electromyography sensor and vibration module to not make tight contact with the skin. The other end of the limiting rod 725 gradually tapers to facilitate insertion into the slot 712.
[0047] Reference Figure 9 The slider 723 is fixedly connected to the actuating block 74, and the actuating block 74 is slidably connected to the inner wall of the limiting groove 726 opened on the cover plate 72.
[0048] In this preferred embodiment, the toggle block 74 is moved by hand, which drives the slider 723 and the limiting rod 725 to move, and the limiting rod 72 is pulled out of the slot 712. At this time, the cover plate 72 can be opened to release the lock on the pull rope 5, and the pull rope 5 can be adjusted.
Claims
1. A glove for Parkinson's patients, characterized in that: The glove body (1), fixing ring (2), sensor (3), sleeve (4), pull cord (5) and winding mechanism (6) are included. The finger area of the glove body (1) is fixedly connected to the fixing ring (2). The sensor (3) is fixedly connected to the glove body (1) inside the fixing ring (2). The fixing ring (2) is connected to one end of the pull cord (5). The pull cord (5) passes through the sleeve (4) and is fixedly connected to the winding mechanism (6). The outer wall of the sleeve (4) is fixedly connected to the glove body (1). The winding mechanism (6) is used to wind up the pull rope (5).
2. The Parkinson's patient wear gloves as described in claim 1, characterized in that: The fixed ring (2) has an annular groove (21) inside, and a fixed block (22) is fixedly connected to the inner wall of the annular groove (21). The fixed block (22) is fixedly connected to one end of the pull rope (5), and the pull rope (5) passes through the through hole (23) and the sleeve (4).
3. The Parkinson's patient wear gloves as described in claim 1, characterized in that: The winding mechanism (6) includes a housing (61), a first rotating shaft (62), a second rotating shaft (63), a first gear (64), a second gear (65), and a winding drum (66). The outer wall of the housing (61) is fixedly connected to the wrist position of the glove body (1). The two ends of the first rotating shaft (62) and the second rotating shaft (63) are respectively rotatably connected to the inner wall of the housing (61). Multiple winding drums (66) are respectively provided on the first rotating shaft (62) and the second rotating shaft (63). The first rotating shaft (62) is fixedly connected to the first gear (64), the first gear (64) meshes with the second gear (65), and the second gear (65) is fixedly connected to the second rotating shaft (63).
4. The Parkinson's patient wear gloves as described in claim 3, characterized in that: The first rotating shaft (62) and the second rotating shaft (63) are respectively provided with a first receiving cavity (631). The bottom wall of the first receiving cavity (631) is fixedly connected to one end of the first spring (632), and the other end of the first spring (632) is fixedly connected to the movable plate (633). The movable plate (633) is fixedly connected to one side of the clamping plate (634). The inner wall of the winding drum (66) is provided with an internal gear (661), and the internal gear (661) meshes with the other side of the clamping plate (634).
5. The Parkinson's patient wear gloves as described in claim 4, characterized in that: The first gear (64) meshes with the third gear (67), the third gear (67) is fixedly connected to the micro motor (68), and the micro motor (68) is fixedly connected to the inner wall of the housing (61).
6. The Parkinson's patient wear gloves as described in claim 5, characterized in that: The outer wall of the fixed ring (2) is fixedly connected to the locking mechanism (7), which is used to lock the pull rope (5).
7. The Parkinson's patient wear gloves as described in claim 6, characterized in that: The locking mechanism (7) includes a base (71) and a cover plate (72). The base (71) is hinged to the cover plate (72). A first guide groove (711) is provided on the base (71), and a second guide groove (721) is provided on the cover plate (72).
8. The Parkinson's patient wear gloves as described in claim 7, characterized in that: The inner walls of the first guide groove (711) and the second guide groove (721) are respectively fixedly connected with conical teeth (73), and multiple conical teeth (73) are provided.
9. The Parkinson's patient wear gloves as described in claim 8, characterized in that: The base (71) has a slot (712) and the cover plate (72) has a second receiving cavity (722). The inner wall of the second receiving cavity (722) is slidably connected to two sliders (723). The two sliders (723) are respectively fixedly connected to the two ends of the second spring (724). The sliders (723) are fixedly connected to one end of the limiting rod (725). The limiting rod (725) slides through the cover plate (72) and the other end of the limiting rod (725) is slidably connected to the slot (712).
10. The Parkinson's patient wear gloves as described in claim 9, characterized in that: The slider (723) is fixedly connected to the actuating block (74), and the actuating block (74) is slidably connected to the inner wall of the limiting groove (726) opened on the cover plate (72).