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Establishment and application of rehabilitation evaluation system for nonspecific low back pain

Establishment and application of rehabilitation evaluation system for nonspecific low back pain

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300076683
Enrollment
Unknown
Registered
2023-10-16
Start date
2022-01-01
Completion date
Unknown
Last updated
2023-10-22

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

Conditions

Nonspecific low back pain

Interventions

Individualized exercise therapy group:Individualized exercise training
Regular exercise training group:Routine core movement training

Sponsors

Zhongnan Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 55 Years

Inclusion criteria

Inclusion criteria: (1) Patients meeting diagnostic criteria; (2) Aged between 20 and 55, able to actively cooperate with treatment; (3) Has not undergone surgery or received any physical, medical or exercise therapy in the past 4 weeks; (4) Understand and sign informed consent.

Exclusion criteria

Exclusion criteria: (1) acute lumbar sprain, severe pain and spasms; (2) definite diagnosis of lumbar disc herniation, spondylolysis, spinal stenosis, spondylolisthesis, etc.; (3) serious injury of skeletal muscle system, such as fracture, dislocation and muscle ligament tear, etc.; (4) serious bone diseases, such as osteoporosis; (5) active inflammation, such as rheumatoid arthritis, ankylosing spondylitis, gout, etc.; (6) Central nervous diseases, such as spinal cord injury, myelitis, cauda equina damage, etc.; (7) complicated with visceral diseases or low back pain caused by visceral diseases; (8) vascular abnormalities, such as visceral vascular diseases, hemophilia, etc.; (9) Progressive aggravation or externalization of symptoms and signs; (10) any type of infection and tuberculosis; (11) primary or secondary tumors; (12) pregnant or lactating women, children; (13) mental disorders; (14) Subjects are subjectively unwilling to cooperate.

Design outcomes

Primary

MeasureTime frame
Oswestry disability index score;

Secondary

MeasureTime frame
Visual analogue scale (VAS) for pain;Brief Health survey Form SF-36;

Countries

China

Contacts

Public ContactHu Yan

Zhongnan Hospital of Wuhan University

392062395@qq.com+86 159 2644 3832

Outcome results

None listed

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