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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06453798
Other study ID # 20230601001
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date June 2024
Est. completion date December 2024

Study information

Verified date June 2024
Source Lingshan County second People's Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


Description:

After being informed of the risks, participants are required to sign an informed consent form. Eligible participants will be randomly assigned to cervical spine operation combined with nerve mobilizatio or cervical spine exercises or neuromobilization on a 1:1:1 ratio.


Recruitment information / eligibility

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.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
cervical spine exercises,Neuromobilization
Cervical spine exercise training is a method to improve the neck function through the patient's self-exercise. Neuromobilization is a technical technique for rehabilitation therapists to loosen the trapped nerves of patients with professional methods.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Quanzheng Chen

Outcome

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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