Transcranial magnetic stimulation for arm and hand function after cerebellar damage

You may qualify if

• 18-100 years old,
• Native English speakers,
• Medically stable to participate in the study. For those with cerebellar disorders:; presenting with a cerebellar disorder including cerebellar stroke; cerebellar disorder onset at least 2 weeks before enrollment.

You can't join if

• Are unable to give consent,
• Have contractures, orthopedic problems, or other impairments that would interfere with the use of the robot or limit the range of joint motion in the potential study arm,
• Presence of medical condition or implant that prevents safe administration of stimulation (history of seizures, and/or taking any of the following medications: lamotrigine (Lamictal), levetiracetam (Keppra), oxcarbazepine (Trileptal), topiramate (Topamax), phenytoin (Dilantin), arbamazepine (Tegretol), valproic acid (Depakote), or phenobarbital (Barbita, Luminal, Solfoton).
• Have any factor that precludes participation in a magnetic resonance imaging (MRI) session (e.g. ferrous metal in the body), or
• Have a medical condition or physical impairment precluding the ability of the participant to complete the required testing.
• Are pregnant Control participants will be excluded for the following condition:; have self-reported history of neurological injury or a developmental disorder