Investigation on rehabilitation consciousness of outpatients and analysis of influencing factors of home rehabilitation for cervical spondylosis

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100050839

Enrollment

Unknown

Registered

2021-09-04

Start date

2021-09-10

Completion date

Unknown

Last updated

2022-05-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical spondylosis

Interventions

Experimental group:Modified home rehabilitation programme

Control group:Traditional home rehabilitation programme

Questionnaire group:No

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Questionnaire group: 1. Have corresponding clinical manifestations of cervical spondylosis; 2. Imaging examination showed degenerative changes of cervical intervertebral disc or intervertebral joint; 3. There is corresponding imaging basis, that is, the clinical manifestations are consistent with imaging abnormalities; cervical spondylosis is not diagnosed if there are only degenerative changes of cervical spine shown by imaging without clinical symptoms of cervical spondylosis; 4. Aged 18-75 years; 5. Volunteer to participate in this study and sign informed consent. Experimental group and control group: 1. Patients with cervical spondylosis who underwent rehabilitation therapy for the first time in the Department of Rehabilitation Medicine from January 2022 to September 2022; 2. Meet the diagnostic criteria for cervical spondylosis of cervical type/radiculopathy; 3. Aged 18-75 years; 4. Voluntarily participate in this study and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Cervical fracture, tuberculosis, tumor or other organic diseases of neuroskeletal muscle, which are harmful to the neck affecting vertebral function; 2. Those with poor compliance, unable to implement home-based rehabilitation program and failing to cooperate with rehabilitation evaluation; 3. Participating in other intervention studies.

Design outcomes

Primary

Measure	Time frame
Neck disability index (NDI);	—

Secondary

Measure	Time frame
Range of motion (ROM);Manual muscle testing (MMT);Numerical rating scale (NRS);Semmes-Weinstein (S-W);Patient specific functional scale (PSFS);Medical Outcomes Study 36-item Short-Form Health Survey (SF-36);Mental rotation;Surface electromyography (sEMG);	—

Countries

China

Contacts

Public ContactXu Lijuan

The Fifth People's Hospital of Yuhang District of Hangzhou

ywykfk@163.com+86 15355817292

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026