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Using Non-invasive Brain Stimulation to Explore Potential Treatments to Reduce Speech Erro

The goal of this study is to find out whether a type of noninvasive brain stimulation can help reduce speech errors, such as repetitions, blocks, and prolongations, in people who stutter. This pilot study will help researchers design future treatments to see if targeting certain brain areas can improve speech fluency.

Condition(s)Stuttering, Fluency Disorder
StatusRecruiting
PhaseNA
Study typeInterventional
SummaryThe goal of this study is to find out whether a type of noninvasive brain stimulation can help reduce speech errors, such as repetitions, blocks, and prolongations, in people who stutter. This pilot study will help researchers design future treatments to see if targeting certain brain areas can improve speech fluency. The study will look at how people speak and behave during both speaking and non-speaking tasks before and after the brain stimulation. Participants will complete an online survey about 24 hours before coming to the clinic. The clinic visit will last about 3 hours and will include three phases. All parts of the study will be audio-recorded. 1. Pre-Testing: Participants will first complete a stuttering evaluation to determine whether they are typical speakers or have a mild, mo
Who can participateInclusion Criteria: * Must be 22 years old or older * May be bi/multilingual but must speak English as dominant language. * Must be diagnosed or suspected of developmental stuttering disorder. Participants will be administered the Stuttering Severity Instrument 4 and categorized as typical speakers or mild, moderate, or severe stutterers. * Must be able to attend the session at the physical location within the clinic Exclusion Criteria: * Patients with preexisting speech/language disorders or previously diagnosed neurological disorders (including but not limited to apraxia of speech, cerebral palsy, dysarthria, tourettes, or any other neurological/motor condition) that affect speech/language (except stuttering) are excluded to minimize the interference of atypical brain activity. * Partici
Ages22 Years
SexAll
Lead sponsorThe University of Texas at Dallas
LocationsRichardson, Texas, United States
Start date2026-03-17
NCT IDNCT07354139
Official listinghttps://clinicaltrials.gov/study/NCT07354139

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