Effects of repetitive transcranial magnetic stimulation on cortical plasticity
Phase 1
- Conditions
- healthy subjects, movement disorders
- Registration Number
- JPRN-UMIN000019733
- Lead Sponsor
- Departemtn of Neurology, the University of Tokyo Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Not provided
Exclusion Criteria
The only absolute contraindication to TMS/rTMS is the presence of metallic hardware in close contact to the discharging coil (such as cochlear implants, or an Internal Pulse Generator or medication pumps). In such instances there is a risk of inducing malfunctioning of such implanted devices.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome measure is cortical plasticity assessed by neurophysiological and behavioural measures up to 3 hours after the intervention.
- Secondary Outcome Measures
Name Time Method