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Acupuncture for Chronic Nonspecific Low Back Pain: A Randomized Controlled Trial.

Acupuncture for Chronic Nonspecific Low Back Pain: A Randomized Controlled Trial.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001273
Enrollment
Unknown
Registered
2026-05-18
Start date
2026-05-30
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

Chronic nonspecific low back pain

Interventions

Sham acupuncture group:Sham acupuncture

Sponsors

First Teaching Hospital of Tianjin University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1)Patients who meet the above diagnostic criteria for cNSLBP with a duration of illness >12 weeks 2) Patients who self-assess their subjective pain intensity as =3 points on the VAS scale during episodes of low back pain 3) Adult patients aged 18 years or older, with no gender restrictions 4) Patients who have not received related acupuncture treatment in the past month 5) Patients who are conscious, have normal vital signs, can accurately understand the meanings of various scales, and actively cooperate with acupuncture treatment

Exclusion criteria

Exclusion criteria: 1)Subacute and acute low back pain (duration =12 weeks) 2) Patients with low back pain (LBP) accompanied by radicular dysfunction 3) Chronic low back pain caused by specific spinal lesions, such as infections, tuberculosis, fractures, lumbar spine or intraspinal tumors, and ankylosing spondylitis 4) Patients with low back pain secondary to other systems (urinary, reproductive, or immune systems) 5) Patients with a history of lumbar spine surgery, metallic implants in the body, or women who are breastfeeding or pregnant 6) Patients with severe skin diseases (e.g., erysipelas, severe eczema, severe dermatitis, severe psoriasis, and severe urticaria-lupus) 7) Patients who are unconscious, extremely weak, unable to express subjective symptoms of discomfort; or those with aphasia or severe visual, auditory, or cognitive impairments, making it impossible to complete various assessment scales as required.

Design outcomes

Primary

MeasureTime frame
Visual Analogue Scale;

Secondary

MeasureTime frame
Oswestry disability index;Surface Electromyography;Short Form-36 Health Survey;Depression, Anxiety, and Stress Scale;

Countries

China

Contacts

Public ContactChen Youyi

First Teaching Hospital of Tianjin University of Traditional Chinese Medicine

cherrychen99@sina.com13502118162

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Jun 11, 2026