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Clinical study on repeated peripheral magnetic stimulation for non-specific low back pain

Clinical study on repeated peripheral magnetic stimulation for non-specific low back pain

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400093968
Enrollment
Unknown
Registered
2024-12-15
Start date
2025-01-01
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Non-specific low back pain

Interventions

Sponsors

First Affiliated Hospital of Air Force Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 60 Years

Inclusion criteria

Inclusion criteria: I. Nonspecific Low Back Pain Patients: 1. Age between 20-60 years old; 2. Average Numerical Rating Scale (NRS) score = 3 in the last month; 3. Average Oswestry Disability Index (ODI) score = 10 in the last month; 4. Meet the diagnostic criteria for nonspecific low back pain; 5. Capable of cooperating to complete treatment and assessment; 6. Signed the informed consent form. II. Healthy Subjects: 1. Basic conditions match those of nonspecific low back pain patients; 2. No symptoms of low back pain in the past 3 months; 3. Capable of cooperating to complete assessments; 4. Signed the informed consent form.

Exclusion criteria

Exclusion criteria: Exclusion Criteria: 1. Spine-specific conditions: such as degenerative spine diseases, lumbar disc herniation, lumbar spinal stenosis, spondylolisthesis, metabolic diseases (osteoporosis, osteomalacia, gout, etc.), spinal trauma (vertebral fractures, etc.), osteoporotic vertebral compression fractures of the thoracic and lumbar spine, spinal tumors (primary and metastatic), spinal infectious diseases (pyogenic spondylitis, disc infection, tuberculous spondylitis, etc.), ligamentous ossification of the spine, spinal deformities (scoliosis, kyphosis, etc.), non-infectious spondyloarthropathies (ankylosing spondylitis, sacroiliitis with sclerosis, etc.), muscle and fascia-related conditions, history of spinal surgery; 2. Neurological conditions: spinal cord tumors, cauda equina tumors, etc; 3. Visceral-related conditions: urinary system diseases (renal calculi, ureteral calculi, pyelonephritis, etc.), gynecological diseases (endometriosis, etc.), others (intra-abdominal lesions, retroperitoneal lesions, etc.); 4. Vascular conditions: abdominal aortic aneurysm, dissecting aneurysm, etc; 5. Psychogenic conditions: depression, hysteria, etc; 6. History of local magnetic stimulation treatment within the past 3 months; 7. Contraindications for magnetic stimulation treatment (history of epilepsy, cochlear implants, local metal implants, cardiac implants, pregnancy and the puerperal period, etc.); 8. Currently using analgesic and/or muscle relaxant medications; 9. Local skin damage or sensory abnormalities.

Design outcomes

Primary

MeasureTime frame
Numeric Rating Scale, NRS;

Secondary

MeasureTime frame
Pressure-pain-threshold, PPT;lumbar position sense;Lumbar joint range of motion;Lumbar muscle structure;The 12-item Short Form Health Survey, SF-12;Lumbar muscle structure;EuroQol-5Dimension,EQ-5D;Oswestry disability index, ODI;Patient Health Questionnaire - 9 items,PHQ -9;Generalized anxiety disorder subscale, GAD-7;Fear avoidance belief's questionnaire,FABQ;Pain Catastrophizing Scale,PCS;Pain Self-Efficacy Questionnaire,PSEQ;Pittsburgh Sleep Quality Index,PSQI;Functional near-infrared spectroscopy, fNIRS;Surface electromyography, sEMG".;

Countries

China

Contacts

Public ContactChenguang Zhao

First Affiliated Hospital of Air Force Medical University

edelweiss_zcg@126.com+86 180 6666 6829

Outcome results

None listed

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