Actively Recruiting
Examining Speech Production Errors in Stuttering Using High Definition Transcranial Direct Current Stimulation
Led by The University of Texas at Dallas · Updated on 2026-04-14
50
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating whether a type of noninvasive brain stimulation called High Definition Transcranial Direct Current Stimulation (HD-tDCS) can reduce speech errors like repetitions, blocks, and prolongations in adults who stutter. This pilot study aims to help design future treatments by targeting specific brain areas involved in speech production and motor planning. Participants' speech and behavior will be assessed during speaking and non-speaking tasks before and after the stimulation to understand its effects on speech fluency. Participants will complete an online survey about 24 hours before a clinic visit that lasts about three hours. During the visit, they will first undergo a stuttering evaluation and complete speaking and non-speaking tasks. Then, they will receive a 20-minute session of HD-tDCS, where low electrical currents are applied through electrodes placed on a special cap targeting either the left inferior frontal gyrus (Broca's area) or the presupplementary motor area of the brain. After stimulation, participants will repeat the initial evaluations and tasks. Throughout the study, all sessions will be audio-recorded. Researchers will measure stuttering severity and how well participants perform naming and button-push tasks before and after stimulation. Safety will be monitored, including any dizziness during stimulation. Participants may rinse residual gel from their scalp after the session. Total participation involves the online survey plus the single clinic visit. The study is randomized and single-blinded, aiming to understand how targeted brain stimulation may influence speech production in people who stutter.
CONDITIONS
Brief Title
Using Non-invasive Brain Stimulation to Explore Potential Treatments to Reduce Speech Errors in Adults Who Stutter
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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
- Must be able to attend the session at the clinic location
You will not qualify if you...
- Patients with other speech or neurological disorders affecting speech (e.g., apraxia, cerebral palsy, Tourette's)
- Acquired or neurogenic stuttering
- History of seizures
- Unexplained episodes of loss of consciousness
- Unstable or uncontrolled neuropsychiatric illness
- Implanted brain medical devices or pacemakers
- Electrically, magnetically, or mechanically activated implants
- Cardiac, neural, or medication implants
- Vascular clips or electrically sensitive brain supports
- Serious brain injury
- Skin damage at stimulation sites
- Skin problems like dermatitis, psoriasis, or eczema
- Severe or frequent headaches
- Serious life-threatening diseases (e.g., heart failure, chronic lung disease, active cancer)
- Pregnant women
- Alcohol or controlled substance use within 24 hours of appointment
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - 1 day
Participants receive a single 20-minute session of non-invasive brain stimulation targeting either the speech production area or the motor planning region of the brain to explore potential treatments to reduce speech errors.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Callier Clinical Research Center
Richardson, Texas, United States, 75080
Actively Recruiting
Research Team
C
Christine H Abasi, MS-SLP
J
John Hart Jr., MD
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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