Neuromodulation for Patients With Parkinson's Disease

Part of paid clinical trials in Cambridge, Massachusetts.

Sponsor
Felipe Fregni, MD, PhD, MPH
Study ID
NCT07767006
Status
Not Yet Recruiting

Notify me when recruiting opens

Save your spot on the interest list for this study. We'll keep your details with this study so our team can follow up when recruiting opens.

Not yet recruiting

Add your contact details and location so we can keep your interest tied to this study.

Conditions

  • Adults With Parkinson's Disease

Eligibility Criteria

Sex
ALL
Age
40 Years - 85 Years
Healthy Volunteers
Not accepted

Interventions

  • tDCS combined with TUS — DEVICE
    This study will compare different treatment schedules of combined transcranial direct current stimulation (tDCS) and transcranial ultrasound stimulation (TUS) in participants with Parkinson's disease.

Study Details

This study will compare different treatment schedules of combined transcranial direct current stimulation (tDCS) and transcranial ultrasound stimulation (TUS) in participants with Parkinson's disease. Participants will be randomly assigned to one of four groups: Standard (10 sessions delivered five times per week for two weeks), Distributed (six sessions delivered three times per week for two weeks), Short (five sessions delivered over one week), or Sham (10 sham sessions delivered five times per week for two weeks).

Key Dates

First listed
Aug 17, 2026
Start date
Oct 1, 2026
Status verified
Aug 2026
Primary completion
Jun 30, 2031
Completion
Jun 30, 2032

Study Design

Enrollment
116 participants (estimated)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Standard Protocol
    tDCS combined with TUS for 10 sessions; 5/week for 2 weeks
  • Active Comparator: Distributed Protocol
    tDCS and TUS for 6 sessions; 3/week for 2 weeks
  • Active Comparator: Short Protocol
    tDCS and TUS for 5 sessions over 1 week
  • Sham Comparator: Sham
    Sham stimulation for 10 sessions; 5/week for 2 weeks

Primary Outcome Measure

Improvement in Unified Parkinson's Disease Rating Scale (UPDRS) Part III [ Time Frame: Baseline-adjusted change in UPDRS Part III from end-of-stimulation through 12 weeks. ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Spaulding Rehabilitation Hospital for Continuing CareCambridgeMassachusetts02138-

Find similar trials in Cambridge, MA