Skip to content

Cervical Spine Salvation Project: An Experimental Study on Exercise-Based Intervention for Chronic Non-Specific Neck Pain

Cervical Spine Salvation Project: An Experimental Study on Exercise-Based Intervention for Chronic Non-Specific Neck Pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500103002
Enrollment
Unknown
Registered
2025-05-22
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-05-26

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

Conditions

Chronic neck pain

Interventions

Intervention group:The intervention group implemented an innovative management mode based on cervical stability exercises with elastic band, including a 12-week exercise guidance and supervision once
Control group:The control group will receive only one health education on chronic neck pain management, but no other intervention.

Sponsors

School of Public Health, Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. The participants were workers with chronic neck pain in related institutions and enterprises, whose age range among 20-60 years old. 2. Pain intensity was 3 < VAS < 8(on a 10-point scale) by visual analogue scale (VAS) and disease duration was over 3 months. 3. Participants were required to voluntarily participate in the study and sign a written informed consent to accept the data collection.

Exclusion criteria

Exclusion criteria: 1. Had a history of cervical spine surgery or trauma (e.g., Whiplash injuries, fracture and dislocation). 2. Diagnosed as cervical spondylotic myelopathy or cervical radiculopathy, thoracic outlet syndrome, etc. (Loss of sarcomere strength, sensation, or reflexes on physical examination/previous diagnosis). 3. Patients with major diseases such as cardiovascular disease, Rheumatoid arthritis and cancer. 4. Had pain medication, injections, or rehabilitation of the neck or shoulder in the past 6 months. 5. Individuals with severe acute neck pain (VAS =8), impaired mobility (NDI > 60%) were unable to continue exercise intervention.

Design outcomes

Primary

MeasureTime frame
Intensity of neck pain;

Secondary

MeasureTime frame
Function of neck movement;Quality of life and mental state score;Cross-sectional area of neck muscles;Range of motion of neck;Muscular strength of neck and upper limbs;

Countries

China

Contacts

Public ContactLin Xu

School of Public Health, Sun Yat-sen University

xulin27@mail.sysu.edu.cn+86 136 0247 7650

Outcome results

None listed

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