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A prospective, randomized controlled trial to compare the therapeutic effects of core stable muscle training plus stretching training between remote rehabilitation and outpatient rehabilitation in patients with chronic non-specific low back pain

Application of artificial intelligence system based on remote technology in rehabilitation assessment and training of chronic diseases

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068984
Enrollment
Unknown
Registered
2023-03-03
Start date
2023-04-01
Completion date
Unknown
Last updated
2023-09-04

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

Conditions

chronic non-specific low back pain (NCLBP)

Interventions

Control group:Core muscle stable training and Stretch training and outpatient rehabilitation
Experimental group:Core muscle stable training and Stretch training and telerehabilitation

Sponsors

Chinese Academy of Medical Sciences & Peking Union Medical College
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Aged >=18 years; 2. ODI score at least 20% of the total score; 3. VAS>=3 points; 4. Pain for more than 3 months; 5. Able to stand or walk without assistance; 6. Able to independently sign informed consent; 7. Able to use tele-rehabilitation diagnosis and treatment system.

Exclusion criteria

Exclusion criteria: 1. Rheumatic immune diseases (including rheumatoid arthritis, ankylosing spondylitis); 2. Spinal deformity, spinal structure slip, spinal fracture history, spinal tumor; 3. Herniated disc with pain, numbness (i.e., symptomatic disc herniation); 4. Nervous system disease requires hospitalization; 5. Patients with cognitive dysfunction (those with normal cognitive function as assessed by the Simple State Examination Scale (MMSE), i.e., those with scores greater than 27); 6. Osteoporosis; 7. Cancer; 8. Lower back pain due to trauma; 9. Long-term use of steroids or anticoagulants.

Design outcomes

Primary

MeasureTime frame
Oswestry Disability Index;

Secondary

MeasureTime frame
Numerical Pain Rating Scale;Medical Outcomes 36-Item Shot-Form Health Survey;Fear-avoidance Belief Questionnaire;

Countries

China

Contacts

Public ContactChen Lixia

Chinese Academy of Medical Sciences & Peking Union Medical College

clx727@126.com+86 186 1267 1460

Outcome results

None listed

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