Clinical trial Recruiting at 1 site Phase 1 Interventional Ages 18 to 65

Aripiprazole and sensorimotor function in adults who stutter

Official title: Dopamine and Sensorimotor Function in Stuttering

Run by University of California, San Francisco · NCT07215884 · Data updated 2026-11-12

We will test whether a single 10 mg dose of aripiprazole versus placebo changes speech sensorimotor processing and improves fluency in adults who stutter.

Quick facts

PhasePhase 1
Study typeInterventional
Ages18 Years to 65 Years
SexAll
Enrollment25 (estimated)
SponsorUniversity of California, San Francisco
Academic / other
Locations1 site (San Francisco, California)
StatusRecruiting
StartedSeptember 30, 2025
Main results expectedJune 30, 2027
Study endsAugust 30, 2027
Registry record updatedAugust 19, 2026
Trial IDNCT07215884 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18–65 who are native American English speakers with confirmed childhood-onset stuttering, normal hearing, and no other neurological, psychiatric, or dopaminergic medication use are the intended participants.

Probably not a fit

People with other speech-language-hearing disorders, neurological or psychiatric diagnoses, or who are taking dopaminergic agents or benzodiazepines are excluded and unlikely to benefit from this specific intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Adults who stutter will receive a single 10 mg dose of aripiprazole or a placebo and undergo measurements of speech fluency and sensorimotor responses. Eligible participants are native American English speakers aged 18–65 with childhood-onset stuttering and normal hearing; people on dopaminergic drugs or with other neurological/psychiatric conditions are excluded. The study uses behavioral tasks and neurophysiologic measures at the Biomagnetic Imaging Lab to probe auditory feedback processing and speech prediction. The approach aims to determine whether short-term dopamine modulation or auditory feedback manipulations can transiently enhance fluency and related sensorimotor function.

Why it matters

Potential benefit: If successful, this could point to medication-plus-behavior approaches that reduce stuttering severity and improve speech motor control for adults.

How similar studies have gone: Prior small studies of dopamine-modulating antipsychotics have reported some improvements in stuttering, but using aripiprazole for stuttering is relatively novel and not well established.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* native speakers of American English
* for adults who stutter, presence of stuttering will be confirmed, with onset before age 6 years
* Normal hearing
* Ages of 18 to 65 years
* healthy adults without hearing-language difficulties

Exclusion Criteria:

* self-reported speech-language-hearing difficulties other than stuttering
* self-reported neurological or psychological problems
* other medications (drugs that affect dopaminergic system and/or benzodiazepines)

Where it's running

  • Biomagentic Imaging Lab
    San Francisco, California, United States
    Recruiting

Study contacts

  • Principal investigator: John Houde, PhD — University of California, San Francisco
  • Study coordinator: Natalie Brunwin, MS
  • Email: snl-bil@ucsf.edu
  • Phone: 4154766888

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.