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Clinical Efficacy of Traditional Chinese Medicine Deqi Acupuncture for Individuals with Chronic Non-specific Low Back Pain: A Randomized Controlled Trial

Clinical Efficacy of Traditional Chinese Medicine Deqi Acupuncture for Individuals with Chronic Non-specific Low Back Pain: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000766
Enrollment
Unknown
Registered
2025-04-17
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-04-28

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

Interventions

Experimental group:Standardized magneto-vibration-thermal physical therapy + traditional chinese medicine Deqi Acupuncture therapy
Control group:Standardized magneto-vibration-thermal physical therapy + sham acupuncture

Sponsors

The Second Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) Aged between 18 and 75 years old (inclusive); 2) Meeting the diagnostic criteria for Chronic Non-Specific Low Back Pain (CNLBP); 3) The score on the Visual Analog Scale (VAS) is = 4 cm; 4) Being able to comply with the research protocol and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1) Radicular pain or progressive neurological deficits; 2) Diagnosed with severe spinal pathological diseases (cancer, recent vertebral fractures, spinal infections, or inflammatory spondylitis); 3) Presence of severe chronic diseases (cancer; severe cardiovascular, cerebrovascular, liver, or kidney diseases; or diabetic neuropathy); 4) History of alcohol/drug dependence or treatment for mental disorders (schizophrenia, dementia, or epilepsy); 5) Chronic Non-Specific Low Back Pain (CNLBP) is not caused by spinal or soft tissue diseases (trauma, ankylosing spondylitis, fibromyalgia, rheumatoid arthritis, or gout); 6) Presence of abnormal blood coagulation function (such as hemophilia) and severe skin diseases on the lower back; 7) Having undergone lumbar spine surgery within one year or having planned surgery during the research period; 8) Pregnant or planning to become pregnant; 9) Having received treatment for low back pain within one month (such as electrotherapy, exercise, manipulative therapy, splint treatment, massage, etc.); 10) Participating in other clinical trials simultaneously.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale,VAS;

Secondary

MeasureTime frame
Pain Catastrophizing Scale, PCS;blinding index;Ultrasound shear wave elastography, SWE;SF-12Quality of Life Scale;Massachusetts general hospital acupuncture sensation scale, MASS;Roland–Morris Disability Questionnaire, RMDQ;

Countries

China

Contacts

Public ContactChongwu Xiao

The Second Affiliated Hospital of Guangxi Medical University

19811941276@163.com19811941276

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Jun 4, 2026