Magnetic stimulation reduces compulsive behaviors

Trial ID
NCT06237868
Official Title
The Effects of High-Frequency Repetitive Transcranial Magnetic Stimulation on Impulse Control Disorders in Parkinson's Disease Patients on Dopamine Replacement Therapy.
Goal
Magnetic stimulation reduces compulsive behaviors
Phase
NA
Status
RECRUITING
Sponsor
West Virginia University
Study Type
INTERVENTIONAL
Enrollment
20 participants
Conditions
Impulse Control Disorder, Parkinson Disease
Interventions
rTMS Active, rTMS Sham

Plain-Language Summary

The goal is to reduce impulse control problems like gambling, compulsive shopping, hypersexuality, punding, or dopamine dysregulation syndrome that can arise while on dopamine replacement therapy. The approach uses high-frequency repetitive transcranial magnetic stimulation, sending repeated magnetic pulses to boost activity in frontal brain regions involved in self-control, such as the dorsolateral prefrontal cortex, with active stimulation compared to a sham procedure, and it does not change your levodopa or other dopamine meds. Adults 18 and older with clinician-confirmed Parkinson's who are on dopamine-replacement therapy and have clinician-diagnosed impulse control behaviors can enroll, provided they have mild or no depression (BDI ≤14), reasonable cognition (MoCA ≥20), and no seizure history, major psychiatric illness, significant brain lesions or recent TMS, pregnancy, intracranial metal, or medications that raise seizure risk.

Locations

  • West Virginia University Hospitals, Morgantown, West Virginia, United States

Frequently Asked Questions

What is this trial testing?
This trial is studying rTMS Active. The goal is to reduce impulse control problems like gambling, compulsive shopping, hypersexuality, punding, or dopamine dysregulation syndrome that can arise while on dopamine replacement therapy. The approach uses high-frequency repetitive transcranial magnetic stimulation, sending repeated magnetic pulses to boost activity in frontal brain regions involved in self-control, such as the dorsolateral prefrontal cortex, with active stimulation compared to a sham procedure, and it does not change your levodopa or other dopamine meds. Adults 18 and older with clinician-confirmed Parkinson's who are on dopamine-replacement therapy and have clinician-diagnosed impulse control behaviors can enroll, provided they have mild or no depression (BDI ≤14), reasonable cognition (MoCA ≥20), and no seizure history, major psychiatric illness, significant brain lesions or recent TMS, pregnancy, intracranial metal, or medications that raise seizure risk.
Who can participate?
Participants must be at least 18 Years.
Where is this trial located?
This trial is recruiting at 1 location.
Does it cost anything to join?
No. There is no cost to participate. Study-related care and treatment are provided at no charge.
How long does the trial last?
This trial is estimated to last approximately 2 years.

View on ClinicalTrials.gov