An AI-assisted wearable device for pain treatment

Abstract

The present application relates to the field of auxiliary wearing, in particular to a pain treatment AI auxiliary wearing device, which comprises a watch case, the upper end of the watch case is open, a circular groove is formed in the inner bottom wall of the watch case, a sensing assembly for monitoring the vital sign parameters of a patient is arranged on the inner wall of the circular groove, and a central control board with an annular cross section is arranged on the inner side wall of the watch case, the central control board is electrically connected with the sensing assembly, the central control board controls the sensing assembly through electrical connection, a screen for displaying the watch control interface and parameters is arranged on the watch case, and a control assembly for controlling the central control board is further arranged on the watch case, the heart rate, blood oxygen, steps and sleep of the user can be monitored in real time through the sensing assembly, the monitoring information can be synchronized to the central control board, then the central control board can transmit the information to the screen for display, and the patient can view conveniently.

Description

Technical Field

[0001] This invention relates to the field of wearable aids, and in particular to an AI-assisted wearable device for pain treatment. Background Technology

[0002] Currently, pain patients, especially those with cancer pain, often experience poor treatment outcomes due to a lack of proper planning and medication. This is primarily because of inappropriate medication use and the inability of doctors to monitor patients' conditions in real time. Patients often fail to perceive their own discomfort, such as heart rate, blood oxygen levels, blood pressure, and pain symptoms, during treatment and medication. This crucial information is essential for doctors to determine the next steps in treatment. Currently, medical staff typically need to proactively inquire about these details from patients. However, some elderly patients or those in poor mental condition are unable to effectively and accurately express their physical condition.

[0003] Furthermore, during treatment, patients usually need to take medication on time, such as painkillers. However, some patients fail to take their medication on time or forget to take it, resulting in poor treatment outcomes. Moreover, without the assistance of medical staff, patients often mix medications that cannot be mixed due to a lack of professional pharmacological knowledge, leading to poor treatment results or even poisoning. In addition, during treatment or rehabilitation, the patient's daily exercise and sleep patterns are also important indicators for judging their recovery progress.

[0004] While existing technologies offer devices or methods to address these issues, their functions are somewhat fragmented. For instance, sleep and heart rate can be monitored using existing fitness trackers, while medication reminders and combinations can be recorded and reminded via mobile phones or other electronic devices. However, most patients are in poor mental condition during their illness and lack the energy to use these devices, and the aforementioned electronic devices are also quite complex for the elderly, who may not know how to use them.

[0005] Therefore, based on the above description, there is a lack of wearable monitoring devices that can integrate the above functions and are easy for most patients to use.

[0006] Therefore, based on the above-stated viewpoints, there is still room for improvement in existing AI-assisted wearable devices. Summary of the Invention

[0007] To address the aforementioned issues, this invention provides an AI-assisted wearable device for pain management, comprising a watch case with an open upper end and a circular groove on the inner bottom wall. A sensing component for monitoring a patient's vital signs is disposed on the inner wall of the circular groove. A central control board with a ring-shaped cross-section is disposed on the inner side wall of the watch case, and the central control board is electrically connected to the sensing component, controlling the sensing component via the electrical connection. A screen for displaying the watch's control interface and parameters is provided on the watch case, and a control component for operating the central control board is also provided on the watch case.

[0008] The control components include an annular groove on the watch case, in which a turntable is rotatably mounted. The watch case also has an L-shaped through groove that communicates with the annular groove, with one side of the through groove extending to the inside of the watch case and corresponding to the central control panel.

[0009] Preferably, the control assembly further includes a control plate slidably disposed in the through groove and connected to one side of the turntable. The outer diameter of the central control plate is provided with several contact plates distributed along its axis and one end located in the through groove. The contact plates are provided with contact grooves with U-shaped cross sections. The side of the control plate close to the contact plate is inclined. The control plate sends control commands to the central control plate by contacting the contact plates. The outer side of the turntable is also provided with several friction patterns evenly distributed around its center.

[0010] Preferably, the outer diameter of the central control board is provided with an alarm plate located in an annular groove on one side, and the alarm plate is also provided with a contact groove, and a barrier plate is provided on one side of the alarm plate and an adjacent contact plate.

[0011] Preferably, the sensing component includes an arc-shaped cover disposed on the inner wall of the circular groove, and the arc-shaped cover is made of transparent glass. One side of the arc-shaped cover passes through the circular groove and is located on the outside of the watch case, and the other side of the arc-shaped cover is electrically connected to the central control board.

[0012] Preferably, a heart rate monitoring device, a blood oxygen monitoring device, a step count monitoring device, and a sleep monitoring device are installed inside the arc-shaped cover, and the heart rate monitoring device, blood oxygen monitoring device, step count monitoring device, and sleep monitoring device are all electrically connected to the central control board through the arc-shaped cover.

[0013] Preferably, a pressing unit for preventing accidental screen operation is provided on the inner wall of the watch case. The pressing unit includes sliding grooves symmetrically opened on the inner wall of the watch case, and the screen is slidably connected to the watch case. A sliding plate located in the sliding groove is provided at the lower end of the screen, and the sliding plate is slidably connected to the sliding groove. A reset push spring is provided between the sliding plate and the bottom wall of the sliding groove.

[0014] Preferably, a transfer plate electrically connected to the central control board is provided on the inner side wall of the central control board. An insertion slot is provided in the middle of the transfer plate, and a push spring rod is provided at the lower end of the screen. An insertion plate that is slidably inserted into the insertion slot is provided at the telescopic end of the push spring rod, and the insertion plate is electrically connected to the central control board through the insertion slot and the transfer plate.

[0015] Preferably, the sliding groove is further provided with a locking component for limiting and locking the sliding plate. The locking component includes two locking grooves symmetrically opened on the inner sidewall of the sliding groove. The sliding plate is provided with a locking cavity, and a locking plate is slidably arranged in the locking cavity. A locking ball located in one of the locking grooves is provided at the end of the locking plate.

[0016] Preferably, a push spring is provided between the snap-fit ​​plate and the inner sidewall of the snap-fit ​​cavity.

[0017] In summary, this application includes at least one of the following beneficial technical effects: I. This invention can monitor a user's heart rate, blood oxygen, steps, and sleep in real time through sensing components, and the monitoring information can be synchronized to the central control board. The central control board can then transmit the information to the screen for display, making it convenient for the patient to view. The screen can also be moved up and down by pressing the unit. That is, the screen is not operable in the initial state. Only after pressing, the locking component limits the screen, and then the screen can be operated, preventing the patient from accidentally operating the device.

[0018] Second, this invention allows users to quickly access preset functions or perform monitoring on the central control panel by rotating a turntable via a control component. This facilitates user operation, reduces the learning curve, and further enhances the applicability of the invention. The scale component allows patients to observe the turntable's rotation angle in real time, and the scale also helps patients input pain levels more quickly and accurately into the central control panel, preventing inaccurate recordings due to incorrect input. Attached Figure Description

[0019] The present invention will be further described below with reference to the accompanying drawings and embodiments.

[0020] Figure 1 This is a schematic diagram of the main structure of the present invention.

[0021] Figure 2 This is a schematic diagram of the central control board of the present invention.

[0022] Figure 3 This is a head-up cross-sectional view of the control component of the present invention.

[0023] Figure 4 This is a schematic diagram of the structure of the control component of the present invention.

[0024] Figure 5 This is a schematic diagram of the sensing component and pressing unit of the present invention.

[0025] Figure 6 This is the present invention. Figure 5 Enlarged view of part of the structure at point A in the middle.

[0026] Figure 7 This is a flowchart of the operation of the present invention.

[0027] Figure 8 This is a schematic diagram of the scale component of the present invention.

[0028] Figure 9 This is a schematic diagram of the camera component of the present invention.

[0029] In the diagram, 1. Case; 10. Central control panel; 11. Screen; 2. Control assembly; 20. Turntable; 21. Control panel; 22. Contact plate; 23. Contact groove; 24. Friction texture; 25. Alarm panel; 26. Barrier plate; 3. Sensing assembly; 30. Arc-shaped cover; 4. Pressing unit; 40. Sliding groove; 41. Sliding plate; 42. Reset push spring; 43. Transmission plate; 44. Push spring rod; 45. Insertion plate; 5. Snap-fit ​​assembly; 50. Snap-fit ​​groove; 51. Snap-fit ​​plate; 52. Snap-fit ​​ball; 53. Push spring; 6. Scale assembly; 60. Scale; 61. Rectangular block; 62. Triangular pointer; 7. Camera assembly. Detailed Implementation

[0030] The following combination Figures 1 to 9 The embodiments of the present invention will be described in detail below.

[0031] This application discloses an AI-assisted wearable device for pain treatment. It is primarily used for real-time monitoring of a patient's body. Technically, it utilizes multiple sensors to monitor the patient's heart rate, blood oxygen levels, steps, and sleep patterns in real time. Furthermore, the control dial allows for quicker operation, significantly lowering the barrier to entry for the wearable device. The ability to move the device up and down by pressing the screen prevents accidental touches, further enhancing its applicability.

[0032] Example 1: Refer to Figure 1 , Figure 2 and Figure 3As shown, the watch includes a case 1, a sensor component 3, a central control board 10, a screen 11, and a control component 2. The upper end of the case 1 is open, and a circular groove is formed in the bottom wall of the inner side of the case 1. The sensor component 3 for monitoring the patient's vital signs is disposed in the inner wall of the circular groove. The central control board 10 with a ring-shaped cross-section is disposed on the inner side wall of the case 1, and the central control board 10 is electrically connected to the sensor component 3. The central control board 10 controls the sensor component 3 through the electrical connection. The case 1 has a screen 11 for displaying the watch's control interface and parameters. That is, the central control board 10 can drive the sensor component 3 to monitor the patient's physical condition, and the monitored information can be transmitted to the central control board 10 for storage, so that the patient can view it on the screen 11. Similarly, the patient can control the central control board 10 through the screen 11 to drive the sensor component 3 for real-time monitoring.

[0033] In addition, the central control panel 10 has a pre-set application, such as a medication reminder, and the central control panel 10 integrates a speaker and a vibrator. Patients can manually set the interval between each dose of this type of medication on the operation interface on the screen 11, and manually record it when taking the medication for the first time. After that, the wristband can remind the patient by ringing or vibrating each time.

[0034] Furthermore, after collecting the monitoring parameters transmitted by the sensor components 3, the central control board 10 generates a statistical chart in the form of a curve graph once a week, which is convenient for patients and medical staff to view.

[0035] The casing 1 is also equipped with a control component 2 for operating the central control panel 10. The control component 2 allows patients to perform quick operations. For example, if a patient encounters an emergency and is unable to operate the screen 11, they can quickly operate the screen 10 through the control component 2.

[0036] Continue to refer to Figure 2 , Figure 3 and Figure 4 As shown, this is the control component 2 used to control the central control module; specifically, the control component 2 includes a turntable 20, a control panel 21, a contact plate 22, a contact groove 23, a friction pattern 24, an alarm plate 25, and a barrier plate 26. An annular groove is formed on the upper end of the watch case 1, and the turntable 20 is rotatably arranged in the annular groove. The turntable 20 can rotate under the limit of the annular groove. The watch case 1 is also provided with a through groove with an L-shaped cross-section that is connected to the annular groove, and one side of the through groove extends to the inner side of the watch case 1 and corresponds to the central control panel 10.

[0037] The control panel 21 is slidably disposed within the through groove and connected to one side of the turntable 20, meaning the control panel 21 can move along with the turntable 20 within the through groove. The central control panel 10 has several contact plates 22 distributed along its axis on its outer diameter, with one end located within the through groove. Each contact plate 22 has a U-shaped contact groove 23. The side of the control panel 21 closest to the contact plate 22 is inclined. The control panel 21 sends control commands to the central control panel 10 through contact with the contact plate 22; that is, the side of the control panel 21 closest to the contact plate 22 is a spring. The telescopic structure allows the end face of the control panel 21 to enter the contact groove 23 after contacting one of the contact plates 22. The corresponding application program can be triggered to run after the control panel 21 indirectly contacts any of the contact plates 22, according to the pre-set program on the central control panel 10. For example, after the patient rotates the turntable 20, the control panel 21 will contact an adjacent contact plate 22, and heart rate monitoring will be performed to facilitate quick operation by the patient. After the patient rotates the turntable 20 again, it will jump to other programs.

[0038] The outer side of the turntable 20 is also provided with several friction grooves 24 evenly distributed around its center. The friction grooves 24 are used to increase the friction coefficient between the patient's palm and the outer side of the turntable 20, making it easier for the patient to rotate the turntable 20 for operation.

[0039] The central control panel 10 has an alarm plate 25 located in an annular groove on one side of its outer diameter. The alarm plate 25 also has a contact groove 23. A barrier plate 26 is provided on one side of the alarm plate 25 and an adjacent contact plate 22. The alarm plate 25 is spaced far from the other contact plates 22 to prevent the patient from accidentally operating the turntable 20. If the user feels unwell, he / she can drive the control panel 21 to contact the alarm plate 25 through the turntable 20, so that the central control panel 10 sends an alarm message to the medical staff, so that the medical staff can quickly rescue the patient.

[0040] The baffle plate 26 is used to block the control panel 21 to indirectly prevent the turntable 20 from rotating too much.

[0041] Reference Figure 5 As shown, the sensing component 3 is used to monitor human vital signs parameters. Specifically, the sensing component 3 includes an arc-shaped cover 30, which is set on the inner wall of the circular groove. The arc-shaped cover 30 is made of transparent glass. One side of the arc-shaped cover 30 passes through the circular groove and is located on the outside of the case 1. The other side of the arc-shaped cover 30 is electrically connected to the central control board 10.

[0042] The arc-shaped cover 30 houses a heart rate monitoring device, a blood oxygen monitoring device, a step count monitoring device, and a sleep monitoring device, all of which are electrically connected to the central control board 10 via the arc-shaped cover 30.

[0043] The sensors carried on the heart rate monitoring device, blood oxygen monitoring device, step monitoring device and sleep monitoring device can penetrate the arc-shaped cover 30 to monitor the patient's limbs, and then transmit the monitoring information to the central control board 10 through the arc-shaped cover 30.

[0044] Furthermore, the heart rate monitoring device, blood oxygen monitoring device, step count monitoring device, and sleep monitoring device are all existing devices, and their uses in this implementation process are as follows: Heart rate monitoring device: The heart rate monitoring device uses sensors to detect electrical signals or changes in blood flow generated by the heartbeat and measures the heart rate in real time.

[0045] Blood oxygen monitoring device: The blood oxygen monitoring device uses an optical sensor to measure the difference in absorption of red and infrared light by hemoglobin, and monitors the oxygen saturation in the blood in real time to help assess respiratory function and oxygenation level.

[0046] Step counting device: The step counting device uses a built-in accelerometer or gyroscope to detect body movement and monitor the intensity of the patient's activity.

[0047] Sleep monitoring device: records the patient's sleep duration and sleep quality.

[0048] Continue to refer to Figure 5 and Figure 6 As shown, a pressing unit 4 for preventing accidental operation of the screen 11 is provided on the inner wall of the watch case 1. Specifically, the pressing unit 4 includes a sliding groove 40, a sliding plate 41, a reset push spring 42, a transmission plate 43, a push spring rod 44, and an insertion plate 45. Two sliding grooves 40 are symmetrically opened on the inner wall of the watch case 1, and the screen 11 is slidably connected to the watch case 1. The lower end of the screen 11 is provided with a sliding plate 41 located in the sliding groove 40, and the sliding plate 41 is slidably connected to the sliding groove 40. A reset push spring 42 is provided between the sliding plate 41 and the bottom wall of the sliding groove 40. That is, in the initial state, the reset push spring 42 pushes the screen 11 to the upper end of the watch case 1 through the sliding plate 41. When the screen 11 is driven by an external force, the screen 11 drives the sliding plate 41 to move down and drive the reset push spring 42 to compress.

[0049] A transmission plate 43 electrically connected to the central control board 10 is provided on the inner wall of the central control board 10. An insertion slot is provided in the middle of the transmission plate 43. A push spring rod 44 is provided at the lower end of the screen 11. An insertion plate 45 is provided at the telescopic end of the push spring rod 44 and is slidably inserted into the insertion slot. The insertion plate 45 is electrically connected to the central control board 10 through the insertion slot and the transmission plate 43. That is, when the screen 11 descends, it drives the push spring rod 44 to move synchronously. The push spring rod 44 drives the insertion plate 45 to be inserted into the insertion slot on the transmission plate 43. This allows the touch module inside the screen 11 to be indirectly electrically connected to the central control board 10, so that the patient can operate the central control board 10 through the screen 11. The program set inside the central control board 10 will run. When the screen 11 is at the initial height, the screen 11 can only display the information collected by the central control board 10 and cannot operate the sensing component 3 through the central control board 10.

[0050] Reference Figure 6 and Figure 7 As shown, the sliding groove 40 is also provided with a locking assembly 5 for limiting and locking the sliding plate 41; specifically, the locking assembly 5 includes a locking groove 50, a locking plate 51, a locking ball 52 and a push spring 53. Two locking grooves 50 are symmetrically opened on the inner side wall of the sliding groove 40. A locking cavity is opened in the sliding plate 41. The locking plate 51 is slidably arranged in the locking cavity. The end of the locking plate 51 is provided with a locking ball 52 located in one of the locking grooves 50. A push spring 53 is provided between the locking plate 51 and the inner side wall of the locking cavity.

[0051] In its initial state, the push spring 53 pushes the locking ball 52 into the upper locking groove 50 via the locking plate 51, limiting the screen 11. When the screen 11 is pressed down to descend, the locking ball 52 moves out of the upper locking groove 50 and then moves to the next locking groove 50, limiting the screen 11 again. At this time, the screen 11 indirectly drives the insertion plate 45 to be inserted into the insertion groove. Therefore, patients and medical staff can operate the central control panel 10 through the screen 11. After the operation is completed, the screen 11 is pressed down again to descend. At this time, the compression force of the reset push spring 42 reaches its limit and no longer presses the screen 11. Then, the reset push spring 42 releases the thrust to push the screen 11 to the initial height, so that the locking ball 52 is locked in the upper locking groove 50 again to limit the screen 11. At this time, the screen 11 cannot be operated to avoid accidental operation by the patient.

[0052] Example 2: Refer to Figure 8As shown, based on Embodiment 1, in order to enable the patient to feel pain and facilitate rapid recording, a scale component 6 is provided on the end face of the watch case 1. Specifically, the scale component 6 includes a scale 60, a rectangular block 61, and a triangular pointer 62. Several scales 60 are evenly distributed on the end face of the turntable 20 along the axis of the turntable 20, and the scales 60 correspond one-to-one with the contact plate 22. Similarly, the dial also has a scale 60 corresponding to the alarm plate 25, and there is a certain distance between it and the other scales 60. A rectangular block 61 is provided on the watch case 1, and a triangular pointer 62 is provided on the rectangular block 61. The triangular pointer 62 corresponds to one of the scales 60.

[0053] When the patient rotates the turntable 20, the scale 60 on the turntable 20 will also move synchronously, so that the patient can know the current rotation range of the turntable 20 by matching the triangular pointer 62 with the scale 60.

[0054] Therefore, according to actual usage needs, multiple contact plates 22 can be set to different functions. For example, after each dose of painkiller, the patient can divide the multiple contact plates 22 into multiple pain levels based on the changes in pain sensation after taking the medication. The scale 60 makes it easy for the patient to observe the current level. The patient can drive the control plate 21 to contact the corresponding level of contact plate 22 through the turntable 20 according to the pain sensation they feel, and record the changes in pain sensation after each dose. This allows medical staff to adjust the dosage based on the collected information.

[0055] Example 3: Based on Examples 1 and 2, the central control board 10 also integrates an AI large model database to monitor the user status through the sensor component 3. The AI ​​large model has the ability to quickly analyze the collected patient medical data, and summarize and analyze it to provide treatment strategies for patients.

[0056] Furthermore, the central control board 10 can wirelessly transmit data. Appropriate software can be installed on the mobile phones of family members and doctors to transmit information synchronously to their mobile phones, making it convenient for family members and doctors to monitor the patient's physical condition in real time.

[0057] Example 4: Refer to Figure 9 As shown in Embodiments 1, 2 and 3, a receiving groove is also provided on one side of the dial, and a camera component 7 is slidably disposed in the receiving groove. The camera component 7 is a 3D Höller rotating camera, which is the prior art. In use, the patient pulls the camera component 7 out of the receiving groove and then rotates the camera component 7 to change its angle.

[0058] The camera component 7 can recognize the patient's face, capture images of changes in the patient's facial expressions, and generate a pain score by comparing different expressions with standardized expressions. This allows the patient to collect pain index data without manually inputting pain values, further increasing the applicability of the invention.

[0059] During operation: First, the sensor component 3 can monitor the user's heart rate, blood oxygen, steps and sleep in real time, and the monitoring information can be synchronized to the central control board 10. Then, the central control board 10 can transmit the information to the screen 11 for display, so that the patient can view it.

[0060] Step 2: The screen 11 can be moved up and down by pressing the unit 4. That is, the screen 11 cannot be operated in the initial state. Only after pressing, the locking component 5 limits the screen 11, and the screen 11 can be operated to prevent the patient from misoperating when wearing the device.

[0061] Step 3: By rotating the turntable 20, the preset functions in the central control board 10 can be quickly called up or monitored by the control component 2, which makes it easier for users to operate the device, reduces the learning cost of the device, and further improves the applicability of the invention.

[0062] Step 4: The scale component 6 allows patients to observe the rotation angle of the turntable 20 in real time. The scale also helps patients to input the pain level more quickly into the central control panel 10 for storage, preventing inaccurate information due to incorrect numerical input.

[0063] It will be apparent to those skilled in the art that the present invention is not limited to the details of the exemplary embodiments described above, and that the invention can be implemented in other specific forms without departing from its spirit or essential characteristics. Therefore, the embodiments should be considered in all respects as exemplary and not restrictive.

[0064] Furthermore, it should be understood that although this specification describes embodiments, not every embodiment contains only one independent technical solution. This narrative style is merely for clarity. Those skilled in the art should consider the specification as a whole, and the technical solutions in each embodiment can also be appropriately combined to form other embodiments that can be understood by those skilled in the art.

Claims

1. A wearable device for pain treatment using AI assistance, comprising a casing (1), characterized in that: The upper end of the watch case (1) is open. A circular groove is provided on the bottom wall of the watch case (1). A sensor component (3) for monitoring the vital signs parameters of the patient is provided on the inner wall of the circular groove. A central control plate (10) with a ring-shaped cross section is provided on the inner side wall of the watch case (1). The central control plate (10) is electrically connected to the sensor component (3). The central control plate (10) controls the sensor component (3) through the electrical connection. A screen (11) for displaying the watch control interface and parameters is provided on the watch case (1). A control component (2) for controlling the central control plate (10) is also provided on the watch case (1). The control component (2) includes an annular groove on the watch case (1), a turntable (20) is rotatably arranged in the annular groove, and a through groove with an L-shaped cross section is also provided in the watch case (1), and one side of the through groove extends to the inside of the watch case (1) and corresponds to the central control plate (10). The inner wall of the watch case (1) is provided with a pressing unit (4) to prevent the screen (11) from being accidentally operated. The pressing unit (4) includes a sliding groove (40) symmetrically opened on the inner wall of the watch case (1). The screen (11) is slidably connected to the watch case (1). The lower end of the screen (11) is provided with a sliding plate (41) located in the sliding groove (40). The sliding plate (41) is slidably connected to the sliding groove (40). A reset push spring (42) is provided between the sliding plate (41) and the bottom wall of the sliding groove (40). The central control board (10) is provided with a transmission plate (43) electrically connected to it on its inner side wall. The transmission plate (43) has an insertion slot in the middle. The screen (11) is provided with a push spring rod (44) at the lower end. The extension end of the push spring rod (44) is provided with an insertion plate (45) that slides into the insertion slot. The insertion plate (45) is electrically connected to the central control board (10) through the insertion slot and the transmission plate (43). The sliding groove (40) is also provided with a snap-fit ​​assembly (5) for limiting and snapping the sliding plate (41). The snap-fit ​​assembly (5) includes two snap-fit ​​grooves (50) symmetrically opened on the inner side wall of the sliding groove (40). The sliding plate (41) is provided with a snap-fit ​​cavity. A snap-fit ​​plate (51) is slidably arranged in the snap-fit ​​cavity. A snap-fit ​​ball (52) located in one of the snap-fit ​​grooves (50) is provided at the end of the snap-fit ​​plate (51). The control assembly (2) further includes a control plate (21) that is slidably disposed in the through groove and connected to one side of the turntable (20). The outer diameter of the central control plate (10) is provided with several contact plates (22) distributed along its axis and one end located in the through groove. The contact plates (22) are provided with contact grooves (23) with U-shaped cross sections. The side of the control plate (21) close to the contact plate (22) is inclined. The control plate (21) sends control commands to the central control plate (10) by contacting the contact plate (22). The outer side of the turntable (20) is also provided with several friction textures (24) evenly distributed around its center. The sensing component (3) includes an arc-shaped cover (30) disposed on the inner wall of the circular groove. The arc-shaped cover (30) is made of transparent glass. One side of the arc-shaped cover (30) passes through the circular groove and is located outside the watch case (1). The other side of the arc-shaped cover (30) is electrically connected to the central control board (10).

2. The AI-assisted wearable device for pain treatment according to claim 1, characterized in that: The central control board (10) has an alarm plate (25) on one side located in an annular groove on its outer diameter, and a contact groove (23) is also provided on the alarm plate (25). A barrier plate (26) is provided on one side of the alarm plate (25) and an adjacent contact plate (22).

3. The AI-assisted wearable device for pain treatment according to claim 1, characterized in that: The arc-shaped cover (30) is equipped with a heart rate monitoring device, a blood oxygen monitoring device, a step count monitoring device and a sleep monitoring device, and the heart rate monitoring device, blood oxygen monitoring device, step count monitoring device and sleep monitoring device are all electrically connected to the central control board (10) through the arc-shaped cover (30).

4. The AI-assisted wearable device for pain treatment according to claim 1, characterized in that: A push spring (53) is provided between the snap-fit ​​plate (51) and the inner wall of the snap-fit ​​cavity.

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