Actively Recruiting

Phase Not Applicable
Age: 18Years - 99Years
All Genders
NCT03452202

Using tDCS in Speech-based Stroke Rehabilitation

Led by NYU Langone Health · Updated on 2025-07-29

24

Participants Needed

2

Research Sites

407 weeks

Total Duration

On this page

Sponsors

N

NYU Langone Health

Lead Sponsor

N

National Institute on Deafness and Other Communication Disorders (NIDCD)

Collaborating Sponsor

AI-Summary

What this Trial Is About

The purpose of this study is to determine whether the effect of treatment for acquired speech impairment can be enhanced by combining effective behavioral treatment with non-invasive brain stimulation. Transcranial direct current stimulation (tDCS), which delivers low-intensity current to the scalp, and is a safe and well-tolerated approach that poses a non-significant risk to participants. tDCS provides low intensity neural stimulation which has been shown to facilitate motor learning in other domains of stroke rehabilitation such as arm motor learning but the potential to enhance speech motor learning has not been explored. This will be examined with a series of single-case experimental designs.

CONDITIONS

Official Title

Using tDCS in Speech-based Stroke Rehabilitation

Who Can Participate

Age: 18Years - 99Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Right-handed
  • Monolingual (English)
  • Single left-hemisphere CVA
  • A minimum of six months post-stroke
  • Clinical diagnosis of apraxia of speech
  • Normal speech perception
  • Passing score on the hearing screening.
Not Eligible

You will not qualify if you...

  • Diagnosis of laryngeal voice disorder
  • Dysarthria
  • History of speech impairment prior to CVA
  • Damaged skin at site of stimulation
  • Presence of electrically or magnetically activated implant (including pacemaker)
  • Metal in any part of the body
  • Family history of medication-resistant epilepsy
  • Past history of seizures or unexplained loss of consciousness

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

New York University School of Medicine

New York, New York, United States, 10016

Actively Recruiting

2

Burke Rehabilitation Hospital

White Plains, New York, United States, 10605

Actively Recruiting

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Research Team

B

Buchwald Lab

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

NON_RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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