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The neuroimaging study of transcranial magnetic stimulation on depression in Parkinson's disease

The neuroimaging study of transcranial magnetic stimulation on depression in Parkinson's disease

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087151
Enrollment
Unknown
Registered
2024-07-22
Start date
2024-07-29
Completion date
Unknown
Last updated
2024-07-29

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

Conditions

Parkinson's disease

Interventions

Experimental group(Stage1):Repetitive transcranial magnetic stimulation
Experimental group(Stage2):Repetitive transcranial magnetic stimulation
Control group(Stage2):False stimulation

Sponsors

The Affiliated Brain Hospital of Nanjing Medical University (Nanjing Brain Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Meets the diagnostic criteria of the Parkinson's Disease Society Brain Bank in the UK; 2. Meets the diagnostic criteria for depression in the Diagnostic and Statistical Manual of Mental Disorders, 4th edition (DSM-IV); 3. If the subject is taking oral PD medication, they must have a stable PD medication regimen for at least 28 days and maintain the regimen unchanged during treatment and follow-up; 4. Being able to sign informed consent forms for research.

Exclusion criteria

Exclusion criteria: 1. Secondary Parkinson's syndrome or Parkinson's syndrome accompanied by multiple system atrophy, progressive supranuclear palsy, and other diseases; 2. Merge serious cardiovascular, respiratory, digestive and other diseases; 3. Implant any cardiac pacemaker, deep brain stimulator, or other TMS therapy contraindications; 4. Accompanied by dementia or severe mental symptoms; 5. Have received any antidepressant treatment within 2 months prior to screening; 6. Those who are unable to cooperate in completing clinical scale assessments, imaging examinations, or follow-up.

Design outcomes

Primary

MeasureTime frame
HAMD-24 efficacy and response rate;

Secondary

MeasureTime frame
HAMD-24 score reduction rate;HAMA score reduction rate;

Countries

China

Contacts

Public ContactWeiguo Liu

Department of Neurology, Affiliated Brain Hospital of Nanjing Medical University

liuweiguo1111@sina.com+86 139 1472 5569

Outcome results

None listed

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