Safety and Feasibility of Tele-supervised Home-based Transcranial Direct Current Stimulation in Parkinson's Disease

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The goal of this clinical trial is to learn whether home-based transcranial direct current stimulation (tDCS) is safe and practical for people aged 40 to 70 years with Parkinson's Disease. The study aims to find out if participants can use the tDCS device at home without serious side effects and whether it is easy for them to use on their own. Participants will first attend an in-person visit to learn how to use the tDCS device. They will then use the device at home once a day for 20 minutes over seven consecutive days. Video calls on days 2 and 3 will provide support and supervision. After each session, participants will complete brief online questionnaires about any side effects and how easy the device was to use. The study will also check if using tDCS at home improves motor symptoms in Parkinson's Disease by using a standard movement assessment.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 40
Maximum Age: 70
Healthy Volunteers: f
View:

• Patients with the diagnosis of Parkinson's disease, aged between 40 and 70, who provide verbal and written informed consent will be included. Patients should have access to a computer system for video calls and completing the questionnaires, and they must be able to use it.

Locations
United States
Massachusetts
Center for Brain Circuit Therapeutics, Department of Neurology, Brigham & Women's Hospital
RECRUITING
Boston
Contact Information
Primary
Leila Montaser Kouhsari, MD, PhD
lmontaser@bwh.harvard.edu
(617) 732-7547
Time Frame
Start Date: 2025-02-06
Estimated Completion Date: 2025-09-01
Participants
Target number of participants: 6
Treatments
Experimental: Active tDCS
Subjects receiving active tDCS
Sponsors
Leads: Brigham and Women's Hospital

This content was sourced from clinicaltrials.gov