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Research on Collaborative Prevention and Treatment Technology and Rehabilitation Strategy of Traditional Chinese and Western Medicine Based on the Analysis of Risk Factors for Low Back Pain in Medical Personnel

Research on Collaborative Prevention and Treatment Technology and Rehabilitation Strategy of Traditional Chinese and Western Medicine Based on the Analysis of Risk Factors for Low Back Pain in Medical Personnel

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096175
Enrollment
Unknown
Registered
2025-01-20
Start date
2025-01-30
Completion date
Unknown
Last updated
2025-01-27

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

Conditions

Low back pain

Interventions

Group A Control:Routine Rehabilitation Education
Group A Trial:Integrated Traditional Chinese and Western Medicine Prevention and Control Strategies
Group B Trial:Integrated Traditional Chinese and Western Medicine Prevention and Control Strategies
Group B Control:Routine Rehabilitation Education
Trial C Group:Integrated Traditional Chinese and Western Medicine Prevention and Control Strategies
Group C Control:Conventional Rehabilitation Therapy Interventions

Sponsors

Dongnan University Affiliated Zhongda Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Doctors, nurses, medical technicians, and other personnel who have been engaged in clinical work for more than one year but have not retired; 2. Individuals meeting the diagnostic criteria for low back pain but not yet reaching the surgical indications; 3. Age <= 60 years old; 4. Not taking non-steroidal anti-inflammatory drugs, muscle relaxants, anesthetic sedatives, etc.; 5. Signing an informed consent form and voluntarily participating in this study.

Exclusion criteria

Exclusion criteria: (1) Those who are on vacation, maternity leave and those who are studying in other hospitals; (2) Those who have persistent aggravation of the disease or serious complications due to unknown reasons; (3) Giving up or receiving other treatment during the intervention; (4) pregnancy; (5) Severe spinal lesions, including spinal fractures, lumbar spondylolisthesis, tumors, tuberculosis, ankylosing spondylitis, infections and other lesions, or accompanied by central nervous system injury; (6) History of lumbar surgery or trauma; (7) Parallel participation in other studies.

Design outcomes

Primary

MeasureTime frame
Low Back Pain Questionnaire;

Secondary

MeasureTime frame
Back Muscle Endurance Test;Surface Electromyography;Musculoskeletal Ultrasound;Oswestry Disability Index;Lower Body Flexibility Assessment;Self-rating Anxiety Scale Score;Self-rating Depression Scale Score;

Countries

China

Contacts

Public ContactFan Youqiang

Dongnan University Affiliated Zhongda Hospital

fly_2580@163.com+86 139 1397 5953

Outcome results

None listed

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