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Effect of different weekly frequencies of Chen style-Tai Chi in elderly patients with chronic nonspecific low back pain: a randomized controlled trial

Effect of different weekly frequencies of Chen style-Tai Chi in elderly patients with chronic nonspecific low back pain

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200058190
Enrollment
Unknown
Registered
2022-04-01
Start date
2022-05-01
Completion date
Unknown
Last updated
2023-12-10

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

Conditions

Chronic low back pain

Interventions

Experimental Group:Chen-style Tai Chi(12 weeks)
Control Group:Educational lectures
Experimental Group:ChChen-style Tai Chi(12 weeks)
Experimental Group :ChChen-style Tai Chi(12 weeks)

Sponsors

The Sixth Affiliated Hospital of Sun Yat-Sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Right-handed; 2. Above the age of 60; 3. Non-specific low back pain was confirmed by clinical examination; 4. Discomfort in the back and lumbosacral region with pain symptoms lasting for at least three months and at least three days per week; 5. Pain intensity (VAS) score >=4; 6. No regular (at least 3 times a week, at least 20 minutes each time) exercise of any kind in the past 6 months; 7. MMSE score > 24; 8. Voluntarily participate in this experiment and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Imaging and pathological examination showed the diagnosis of scoliosis, compulsory spondylitis, anterior spine, severe lumbar disc herniation, etc.; 2. The presence of a degenerative disease (e.g. Alzheimer's disease), a diagnosed acute or chronic mental illness or other mental illness; A severe neurological disorder; History of epilepsy, family history of epilepsy, >15 minutes of loss of consciousness; 3. Impaired hearing or vision; 4. Patients who have been diagnosed with rheumatoid arthritis, fibromyalgia and gout; 5. Participants who participated in other clinical trials in the past year and would have affected the outcome of this study.

Design outcomes

Primary

MeasureTime frame
Visual simulation scale;

Secondary

MeasureTime frame
Beck Depression Inventory-II;Pain catastrophizing;Five Facet Mindfulness Questionnaire;Oswestry Disability Index;Quality of life (SF-36);

Countries

China

Contacts

Public ContactYuling Wang

The Sixth Affiliated Hospital of Sun Yat-Sen University

wanruih@163.com+86 13054445587

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 11, 2026