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The effects of Ai Chi on patients with chronic low back pain: A multicenter, randomized, single-blind, three-arm, parallel controlled trial

The effects of Ai Chi on patients with chronic low back pain: A multicenter, randomized, single-blind, three-arm, parallel controlled trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900022921
Enrollment
Unknown
Registered
2019-05-03
Start date
2019-05-15
Completion date
Unknown
Last updated
2019-05-05

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

Hydrotherapy group:Ai Chi
Control group:Physical agents

Sponsors

Guangzhou Sport University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Low back pain (defined as pain and discomfort) of at least 3 months' duration(There is pain, muscle tension or stiffness localized below the costal margin and above the inferior gluteal folds, with or without referred leg pain); 2. Recently did not receive low back pain physical therapy intervention; 3. Aged 20 to 60 years, no gender constraint; 4. Low back pain (when the most painful) NPRS score is more than 4 points; 5. Participate in the trial voluntarily and sign written informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with mental illness and cognitive impairment (MMSE < 24); 2. People with hydrophobia; 3. Lumbar pathology, such as fracture, spinal stenosis, tumor infection, spinal structural abnormalities, etc.; 4. Lumbar dysfunction or pain caused by other diseases; 5. Complex back problems such as sciatica and spinal surgery, major surgery scheduled during treatment or follow-up period; 6. Patients with severe and unstable cardiovascular, renal and liver diseases, and presence of any contraindication to exercise; 7. gestation; 8. Received a low back pain exercise intervention or other physical therapy during the past 3 months.

Design outcomes

Primary

MeasureTime frame
Numerical Pain Rating Scale, NPRS;Roland Morris Disability Questionnaire;

Secondary

MeasureTime frame
The MOS item short from health survey, SF-36;Tampa Scale for Kinesiophobia;Posture control ability;Global Perceived Effect scale;Pain Catastrophizing Scale;Fear Avoidance Beliefs Questionnaire;Pittsburgh Sleep Quality Index;Hospital Anxiety and Depression Scale;Adverse events;

Countries

China

Contacts

Public ContactXiaohui Hou

Guangzhou Sport University

lilyhxh@126.com+86 13822187866

Outcome results

None listed

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