TMS for Parkinson's Disease Apathy
(PDTMSAPATHY Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
The goal of this clinical trial is to develop non-invasive brain stimulation targets for the treatment of apathy, or motivation problems, in Parkinson Disease.The main questions the study aims to answer are:1. Does transcranial magnetic stimulation change effort task performance in Parkinson's Disease patients?2. Is there a link between brain signals and apathy?Participants will* complete questionnaires and assessments* perform an effort task* have their brain activity recorded (EEG)* receive non-invasive brain stimulation (TMS)Researchers will compare two stimulation locations (experimental site and control site) to see if TMS of the experimental site has an effect on apathy. Participants will receive stimulation of both sites (during separate visits).
Will I have to stop taking my current medications?
No, you will not have to stop taking your current medications. Participants must be stable on their Parkinson's medication and any other medications that may influence apathy for at least 4 weeks before the study and remain stable throughout the study.
Is transcranial magnetic stimulation (TMS) safe for humans?
How is the treatment TMS for Parkinson's Disease Apathy different from other treatments?
TMS (Transcranial Magnetic Stimulation) is unique because it is a non-invasive treatment that directly stimulates brain neurons using magnetic fields, unlike traditional medications that often involve oral or injectable drugs. It has shown promise in improving both motor and non-motor symptoms, such as apathy, in Parkinson's disease, which is not typically addressed by standard treatments.678910
What data supports the effectiveness of the treatment Transcranial Magnetic Stimulation (TMS) for Parkinson's Disease?
Research shows that repetitive transcranial magnetic stimulation (rTMS) can improve motor function in Parkinson's disease by modulating brain activity. Studies have demonstrated that rTMS can shorten reaction and movement times in patients, and high-frequency rTMS has shown long-lasting benefits in clinical trials.1011121314
Who Is on the Research Team?
Miriam Sklerov, MD
Principal Investigator
University of North Carolina, Chapel Hill
Are You a Good Fit for This Trial?
This trial is for Parkinson's Disease patients who've had symptoms for at least 5 years, are on stable dopaminergic medication, and can consent in English. Women must be postmenopausal or use contraception. Excluded are those with dementia, epilepsy, brain surgery history, metal implants like pacemakers or deep brain stimulators, severe tremor affecting EEG readings, other causes of parkinsonism or CNS diseases.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive transcranial magnetic stimulation (TMS) at two different sites with a 3-week washout period between sessions
Follow-up
Participants are monitored for changes in goal-directed behavior and reward evaluation after TMS
What Are the Treatments Tested in This Trial?
Interventions
- Transcranial Magnetic Stimulation (TMS)
Transcranial Magnetic Stimulation (TMS) is already approved in United States, European Union for the following indications:
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of North Carolina, Chapel Hill
Lead Sponsor
National Institute of Mental Health (NIMH)
Collaborator