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Repetitive Transcranial Magnetic Stimulation treatment of chronic primary pain: a single-center, prospective double-blind, parallel two-arm randomized controlled trial

Repetitive Transcranial Magnetic Stimulation in the treatment of chronic primary pain

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087589
Enrollment
Unknown
Registered
2024-07-30
Start date
2024-08-01
Completion date
Unknown
Last updated
2024-08-05

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

Conditions

Chronic primary pain

Interventions

Experimental group:Repeat transcranial magnetic stimulation treatment
Control group:Pseudo stimulation treatment

Sponsors

Changhai Hospital of Shanghai
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Age 20-65 years old; 2. The pain lasts or recurs for more than 3 months; 3. Emotional disturbance (Hamilton Anxiety Scale score =8 or Hamilton Depression Scale score =8) or impaired function of daily living (Barthel Index score <100); 4. Pain cannot be explained by other organic pain causes.

Exclusion criteria

Exclusion criteria: 1. Have a history of other definite neurological or psychiatric disorders (e.g. dementia, stroke, Parkinson's disease, severe mental illness, etc.); 2. Those who have severe vision, hearing, aphasia and other physical diseases and cannot successfully complete the neuropsychological test; 3. History of use of any drugs that may affect cognitive function within the last 1 month; 4. Intracranial stents, cochlear built-in hearing aid devices, and cardiac pacemakers do not meet the safety standards for TMS treatment.

Design outcomes

Primary

MeasureTime frame
Pain;

Secondary

MeasureTime frame
Pain;Emotion;Cognitive;Baseline data;

Countries

China

Contacts

Public ContactZhou Shu

Changhai Hospital of Shanghai

kathyrin@163.com+86 134 8223 6605

Outcome results

None listed

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