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Clinical Efficacy of Targeted Repetitive Transcranial Magnetic Stimulation in Individuals with Chronic Non-Specific Low Back Pain: A Randomized Controlled Trial

Clinical Efficacy of Targeted Repetitive Transcranial Magnetic Stimulation in Individuals with Chronic Non-Specific Low Back Pain: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128232
Enrollment
Unknown
Registered
2026-07-16
Start date
2026-07-31
Completion date
Unknown
Last updated
2026-07-20

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

Control group:rTMS sham stimulation + acupuncture
Therapy group:rTMS stimulation + acupuncture

Sponsors

The Second Affiliated Hospital of Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Meet the above-mentioned CNSLBP diagnostic criteria; 2. Male or female aged 18 to 65; 3. The visual analog scale (VAS) for pain is >=4cm and the Oswestry Disability Index (ODI) is >=10 points; 4. Right-handed.

Exclusion criteria

Exclusion criteria: 1. Has a history of lumbar trauma or lumbar and abdominal surgery within the past two years; 2. Radicular pain or progressive neurological deficits; 3. During pregnancy or lactation; 4. There are abnormal coagulation functions (such as hemophilia) and severe skin diseases on the waist; 5. History of severe trauma or tumors; 6. Have received clinical treatment for lower back pain or taken medications that affect balance within the past three months; 7. There is pain in other parts of the body, such as neck pain, knee pain, etc. 8. There are serious chronic diseases (severe cardiovascular, cerebrovascular, liver or kidney diseases; or diabetic neuropathy); 9. Other contraindications to transcranial magnetic stimulation (metal implants in the body, previous epileptic seizures or use of anticonvulsants) or other circumstances that do not cooperate with this study.

Design outcomes

Primary

MeasureTime frame
visual analogue scale, VAS;

Secondary

MeasureTime frame
Pain Catastrophizing Scale, PCS;The performance of balance parameters during posture control tasks;Center for Epidemiological Studies Depression, CES-D;The changes in cortical oxygenated hemoglobin concentration during postural control tasks;Oswestry Disability Index,ODI;SF-12 Health Survey?,SF-12;

Countries

China

Contacts

Public ContactXiao Chongwu

The Second Affiliated Hospital of Guangxi Medical University

pealxiao@foxmail.com+86 19811941276

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026