Radiculopathy, Cervical Clinical Trial
Official title:
Effect of Cervical Exercise Combined With Nerve Mobilization on Cervical Spondylotic Radiculopathy
Verified date | June 2024 |
Source | Lingshan County second People's Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The objective of this clinical trial was to investigate the effects of cervical spine exercises combined with nerve mobilization in patients with radiculopathy. The main questions it aims to answer are: 1. Whether cervical spine operation combined with nerve mobilization is effective for cervical radiculopathy. 2. Is there any difference between cervical spine operation combined with nerve mobilization and single method? The participants were patients with cervical radiculopathy and were divided into three groups in this study. 1. Experimental group: received cervical spine operation combined with nerve mobilization 2. Control group 1: cervical spine exercises were performed 3. Control group 2: received neuromobilization
Status | Not yet recruiting |
Enrollment | 60 |
Est. completion date | December 2024 |
Est. primary completion date | December 2024 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 65 Years |
Eligibility | Inclusion Criteria: 1. Meet the diagnostic criteria of CSR and have no other complications; 2. Age 18-65 years old, gender unlimited; 3. No other treatment for cervical spondylosis in the last 1 month; 4. No previous surgical treatment for cervical spondylosis; 5. Good compliance; 6. Good mental state, no history of mental illness; 7. Informed consent, and sign the informed consent. Exclusion Criteria: 1. does not meet the diagnostic criteria; 2. Women during pregnancy; 3. severe stenosis of the foramen; 4. osteoporosis combined with spinal cord tumor, osteomyelitis; 5. infectious diseases, skin defects, allergies; 6. have serious heart, lung and other important organ dysfunction; 7. unable to cooperate. |
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Quanzheng Chen |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Visual analogue scale | A scale used to evaluate pain. The scale consists of 0 to 10 points, with a higher score indicating greater pain and a lower one. | baseline and 4 weeks | |
Primary | Range of motion | Used to evaluate cervical range of motion | baseline and 4 weeks | |
Primary | Muscle strength | Used to evaluate the strength of the muscles around the neck | baseline and 4 weeks | |
Secondary | Tanaka Yasuhisa Cervical Spondylopathy Symptom Scale | To assess the status of the patient's cervical spine. The scale includes a score of -2 to 20, with the larger the score, the less severe the symptoms associated with the cervical spine. | baseline and 4 weeks | |
Secondary | neck disability index. The total score ranges from 0 (accessibility) to 50 (total paralysis), with higher scores indicating more severe dysfunction. | A scale used to assess the degree of cervical spine dysfunction | baseline and 4 weeks | |
Secondary | the medical outcomes study 36-item short-form health survey | A scale used to assess quality of life.The exact score of the SF-36 varies from item to item, but in general, the higher the score, the better the quality of life. | baseline and 4 weeks |
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