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

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2400093949

Enrollment

Unknown

Registered

2024-12-13

Start date

2025-01-01

Completion date

Unknown

Last updated

2024-12-16

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

Conditions

Non-specific neck pain

Interventions

Experimental group:repetitive peripheral magnetic stimulation, rPMS

Control group:Interferential Current , IFC

Healthy subjects:none

Eligibility

Sex/Gender

All

Age

20 Years to 60 Years

Inclusion criteria

Inclusion criteria: Non specific neck pain patients: 1. Age range: 20-60 years old; 2. The average NRS score last month was >= 3 points; 3. The average NDI score last month was >= 10 points; 4. Meet the diagnostic criteria for non-specific neck pain; 5. Able to cooperate in completing treatment and evaluation; 6. Sign the informed consent form. Healthy participants: 1. Basic information matched with non-specific neck pain patients; 2. There have been no symptoms of neck pain in the past three months; 3. Can cooperate to complete the evaluation; 4. Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Neck pain with a clear cause (such as trauma, discogenic pain with or without lower limb radiating pain, neuropathic pain, etc.); 2. Serious spinal disease (fracture, infectious diseases, ankylosing spondylitis, rheumatoid arthritis or tumor) or previous history of neck surgery; 3. There are serious neurological, cardiovascular, immune metabolic, psychological, or acute/chronic skin diseases present; 4. Vestibular changes, otogenic or idiopathic dizziness/vertigo; 5. History of local magnetic stimulation therapy in the past 3 months; 6. There are contraindications for magnetic stimulation therapy (history of epilepsy, cochlear implants, local metal implants, cardiac implants, pregnancy, etc.); 7. Currently using painkillers and/or muscle relaxants; 8. Local skin damage or sensory abnormalities.

Design outcomes

Primary

Measure	Time frame
Numeric Rating Scale, NRS;	—

Secondary

Measure	Time frame
pressure-pain-threshold, PPT;Neck position perception;Cervical joint range of motion;Maximum isometric contraction muscle strength of neck muscles;Neck muscle structure;the 12-item Short Form Health Survey, SF-12;Neck disability index, NDI;Patient Health Questionnaire - 9 items,PHQ -9;Generalized anxiety disorder subscale, GAD-7;Tampa Scale for Kinesiophobia, TSK;functional near-infrared spectroscopy, fNIRS;Neuroelectrophysiological examination;	—

Measure

Time frame

pressure-pain-threshold, PPT;Neck position perception;Cervical joint range of motion;Maximum isometric contraction muscle strength of neck muscles;Neck muscle structure;the 12-item Short Form Health Survey, SF-12;Neck disability index, NDI;Patient Health Questionnaire - 9 items,PHQ -9;Generalized anxiety disorder subscale, GAD-7;Tampa Scale for Kinesiophobia, TSK;functional near-infrared spectroscopy, fNIRS;Neuroelectrophysiological examination;

—

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