Home-based Transcranial Direct Current Stimulation Open Trial for Behavioral and Cognitive Symptoms in Huntington's Disease

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

The purpose of this study is to assess feasibility, acceptability, and safety of providing transcranial direct current stimulation( tDCS) to Huntingtons Disease (HD) patients in the early to middle stages and to assess the efficacy of tDCS for HD-related behavioral, cognitive and other symptoms

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

⁃ confirmed HD mutation carriers and/or established family history alongside typical symptoms (i.e. chorea) of HD;

⁃ early (stages 1 and 2) or moderate (stage 3) stages according to Shoulson-Fahn

⁃ exhibit mild to moderate behavioral symptoms defined by severity scores in the PBA-S between 1 and 3 for any of the evaluated symptoms and no symptoms with a severity score of 4

⁃ stable doses of medications for at least one month

⁃ Have a caregiver willing to be present during tDCS sessions and answer questionnaires.

• willingness to participate in the study

Locations
United States
Texas
The University of Texas Health Science Center at Houston
RECRUITING
Houston
Contact Information
Primary
Erin Stimming, MD
Erin.E.Furr@uth.tmc.edu
(713) 500-7033
Backup
Thiago Macedo e Cordeiro, MD
macedoecorde@uthscsa.edu
210-450-7055
Time Frame
Start Date: 2023-06-21
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 10
Treatments
Experimental: active tDCS
Sponsors
Leads: The University of Texas Health Science Center, Houston

This content was sourced from clinicaltrials.gov