Frozen Shoulder Clinical Trial
Official title:
Invention of Portable Laser Acupuncture and Joint Mobilization Device on Frozen Shoulder and Therapeutic Effects
the volunteers with frozen shoulder will be recruited to this experiment and use devices under a designed experimental procedure. After subjects use device , R&D team will collect subject feedback, efficacy assessments, and various device data. This step will not only help investigators to improve and refine the device but also find the best operating mode and using standard of the device to help the frozen shoulder patients. Subjects in this study will also enter a designed course of treatment. All patients will be distributed equally and randomly to three groups (control , mobilization device, laser acupuncture plus mobilization device) to receive treatment. All groups receive three therapy sessions per week for 8 consecutive weeks. At last, investigators will compare the differences between the three groups to understand the effect of portable laser acupuncture and joint mobilization device on frozen shoulder.
Status | Recruiting |
Enrollment | 45 |
Est. completion date | January 2022 |
Est. primary completion date | January 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 25 Years and older |
Eligibility | Inclusion Criteria: - Aged over 25 years old - Diagnosed with frozen shoulder and pain in the shoulder - After medical imaging and other related physical examinations, except frozen shoulder, no other shoulder abnormalities and diseases were found. Exclusion Criteria: - Suffer from relevant contraindications of this experiment (such as tumor, cancer, etc.); - Have a history of surgery on the shoulder; - Have a history of trauma on the shoulder (such as: fracture, dislocation, etc.); - Suffer from neuromuscular diseases (such as stroke); - After medical imaging and other related physical examinations, it is found that the shoulder is abnormal and disease other than the frozen shoulder; - received shoulder steroid injections within 6 months. - Suffer from contraindications related to the device used in this study.Patients who meet any of the above conditions will be excluded from this experiment. |
Country | Name | City | State |
---|---|---|---|
Taiwan | Chung Shan Medical University Hospital | Taichung |
Lead Sponsor | Collaborator |
---|---|
Chung Shan Medical University |
Taiwan,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | shoulder range of motions | shoulder range of motion evaluation, including shoulder flexion, abduction, internal rotation, and external rotation. All shoulder range of motions was measured with a standard goniometer. When measured the shoulder range of motion, the researcher force to the patient's upper limbs to make movements. The endpoint of the movement was where the subject began to feel pain. The therapist stopped applying force and record the degrees of shoulder range of motion. | 8 consecutive weeks | |
Primary | pain visual analogue scale | pain visual analogue scale that was used to assess levels of pain. The visual analogue scale has been widely used in clinical and research to assess patients with shoulder pain. It is a grading scale from 0cm to 10cm, presented in front of the subject, and the subject selected the location according to their pain during the last 24 hours (0cm indicating "no pain", 10cm indicating "most pain"). | 8 consecutive weeks | |
Primary | disabilities of the arm, shoulder and hand questionnaire | This questionnaire is mainly composed of 30 disability/symptom scales and has been proven to be reliable and effective in evaluating various upper limb dysfunction patients. The scores obtained for all items will be calculated, ranging from 0 (no disability) to 100 (most severely disabled) to evaluate the subject's shoulder condition | 8 consecutive weeks | |
Primary | constant murley questionnaire | This questionnaire is a tool used to assess the condition of the shoulders. It is a full-point 100-point scale composed of multiple evaluation methods and parameters. The questionnaire is divided into four parts: pain (15 points). activities of daily living (20 points); strength (25 points); and joint mobility (40 points). After completing the questionnaire, add up the scores. The higher the score, the better the shoulder function. | 8 consecutive weeks |
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