What this study is
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.
What's being tested
- Soterix 1x1 line tDCS low-intensity stimulator
Intervention · DEVICE
Introduction of the independent variable (treatment) across three different points in time. Participants will be randomly assigned to have each treatment phase begin after 3, 4, or 6 baseline sessions. This current stimulates the cortex, with anodal stimulation leading to a depolarized state in which neurons are more likely to fire.
- Sham
Intervention · DEVICE
Patients will have two electrodes applied (one anode, one cathode) administering no stimulation
Study details
- Sponsor
- NYU Langone Health
- Conditions
- Apraxia of Speech
- Enrolling
- 24 people
- Starts
- 2019-01-11
- Est. completion
- 2027-04-30
- Design
- Double-blind, non-randomized, crossover
- Record
- View on ClinicalTrials.gov ↗
Who can join
Age 18 Years – 99 YearsSex ALLHealthy volunteers Not acceptedYou may qualify if
- 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.
You can't join if
- Diagnosis of laryngeal voice disorder
- Dysarthria
- History of speech impairment prior to CVA
- Presence of potential tDCS risk factors: damaged skin at site of stimulation;
- Presence of electrically or magnetically activated implant (including pacemaker);
- Metal in any part of their body;
- History of medication-resistant epilepsy in the family;
- Past history of seizures or unexplained spells of loss of consciousness.
Sign in and we'll check these against your records.Full criteria on ClinicalTrials.gov ↗
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Study locations (2)
2 openNew York University School of Medicine
New York, New York, United States
- Buchwald Lab · Contactbuchwald-lab@nyu.edu
- Adam · Contact
- Adam Buchwald, PhD · Principal investigator
RecruitingBurke Rehabilitation Hospital
White Plains, New York, United States
- Josette Hartnett, MPH · Contactjohartnett@burke.org
- Erika Trovato, DO · Principal investigator
Recruiting
Study team
Sponsor
NYU Langone Health
Study ID 17-01474
Principal investigator
Adam Buchwald, MD
NYU Langone Health
Frequently asked questions
The sponsor hasn't published answers to common questions for this trial.