Neck Type Cervical Spondylosis
Conditions
Interventions
Tuina Technique Group:Tuina
Combined Therapy Group:Tuina+Dynamic Rotation-traction Manipulation
Sponsors
Beijing University of Chinese Medicine
Eligibility
Sex/Gender
All
Age
18 Years to 25 Years
Inclusion criteria
Inclusion criteria: 1.Meets the above diagnostic criteria for cervical spondylosis. 2.Aged between 18 and 25 years. 3.Initial visit Visual Analogue Scale (VAS) score = 3 points. 4.Initial visit Neck Disability Index (NDI) score = 9 points. 5.Disease duration less than or equal to 5 years. 6.Having undergone other conservative treatments requires a 1-week washout period. 7.Voluntarily participates in the trial, understands their own condition, cooperates fully with assessment surveys, and persists with treatment and follow-up investigations. 8.The patient is informed and provides signed informed consent.
Exclusion criteria
Exclusion criteria: 1.Individuals who do not meet the aforementioned diagnostic criteria for cervical spondylosis. 2.Those diagnosed with spinal cord-type cervical spondylosis based on MRI findings. 3.Patients with neck or shoulder pain caused by cervical trauma, frozen shoulder, rheumatic myofibrositis, or other conditions not primarily attributable to chronic cervical degeneration. 4.Individuals suspected or confirmed to have tumors, particularly in the neck or brain. 5.Patients with diagnostically unclear spinal injuries accompanied by symptoms of spinal cord damage. 6.Those who experience significant cardiac discomfort during seated traction or the overhead lateral rotation test. 7.Individuals with severe diseases of the cardiovascular, pulmonary, cerebral, hepatic, renal, or hematopoietic systems. 8.Patients with severe skin lesions or dermatological conditions in the area where the manual therapy is to be applied. 9.Individuals with abnormalities or discomfort in spinal structures other than the cervical spine. 10.Those with psychiatric disorders that may interfere with treatment or functional assessment. 11.Individuals unwilling to participate in the study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Range of Motion; | — |
Secondary
| Measure | Time frame |
|---|---|
| Visual Analogue Scale;Neck Disability Index;Range of Motion Score;Pressure Pain Threshold; | — |
Countries
China
Contacts
Public ContactZhou Chunhao
Beijing University of Chinese Medicine
Outcome results
None listed