Stuttering and Neuromodulation
Recruiting now · Not applicable · Has a placebo group
Conditions studied: Stuttering
In brief
The purpose of this study is to collect preliminary data on the efficacy of transcranial direct current stimulation (tDCS) combined with traditional behavioral techniques to reduce stuttering severity and negative impact in adults who stutter. The study also aims to explore neuroplastic changes (i.e., regional activation and functional connectivity) resulting from combined tDCS + speech therapy.
Key facts
- Study ID
- NCT07222163
- Run by
- NYU Langone Health
- People needed
- 16
- Starts
- 2025-09-04
- Expected to finish
- 2027-10-01
- Last updated by the study team
- 2025-10-29
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adults aged 18 to 65 years.
- Diagnosis of developmental stuttering, verified by a licensed speech-language pathologist.
- Mild-to-moderate or greater stuttering severity, defined as a score of 20 or higher on the Stuttering Severity Instrument-Fourth Edition (SSI-4).
- English as a primary language.
- Right-handedness (to minimize variability in neural lateralization).
- Willing and able to attend all study sessions and follow study procedures.
You may not qualify if…
- Have a history of neurological, psychiatric, or medical conditions that are contraindicated for tDCS.
- Are currently taking medications known to affect cortical excitability.
- Have a history of seizures or epilepsy.
- Are pregnant or planning to become pregnant during the study period.
- Have metal implants in the head (excluding dental work) or other contraindications to electrical brain stimulation.
- Any skin disorder or skin sensitive area near stimulation locations.
Where it is running
- NYU Langone Health — New York, New York, United States (enrolling)
Full record on ClinicalTrials.gov
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