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Development and Validation of a Clinical Diagnostic Model for Chronic Low Back Pain Based on ICF Subtypes

Development and Validation of a Clinical Diagnostic Model for Chronic Low Back Pain Based on ICF Subtypes

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500110925
Enrollment
Unknown
Registered
2025-10-22
Start date
2025-10-22
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Low Back Pain

Interventions

Chronic lower back Pain Observation Group:None

Sponsors

Zhongnan Hospital of Wuhan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Age between 18 and 60. 2. Clinically diagnosed as chronic lower back pain (according to the 2021 lower Back Pain Guidelines of the Orthopaedic Division of the American Physical Therapy Association, current lower back pain symptoms lasting more than 6 weeks are classified as chronic lower back pain). It can be clearly classified as one of the following: chronic lower back pain with reduced range of motion, chronic lower back pain with uncoordinated body movement, or chronic lower back pain with radiating pain. 4. Has not undergone surgery or received any medication or physical therapy in the past four weeks. 5. Be capable of completing all evaluations and signing informed consent forms.

Exclusion criteria

Exclusion criteria: 1. Unstable vital signs. 2. Patients with severe cognitive impairment and mental illness. 3. Patients with severe cardiovascular diseases, malignant tumors or other serious diseases that affect survival. 4. Pregnant women. 5. Patients with severe skin damage on the lower back and local infection. 6. Acute fractures, joint dislocations or bone and joint instability, as well as other contraindications that prohibit the measurement of biomechanical data. 7. Those who are unable to cooperate in completing all biomechanical data measurements due to severe pain or fear.

Design outcomes

Primary

MeasureTime frame
Demographic characteristics (such as gender, age, BMI, VAS scores, etc.);Range of Motion;Surface Electromyography Results;Gait Analysis Results;Plantar Pressure Assessment Results;

Countries

China

Contacts

Public ContactTian Jun

Zhongnan Hospital of Wuhan University

852893947@qq.com+86 189 9554 0980

Outcome results

None listed

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