Actively Recruiting

Phase 1
Age: 18Years - 65Years
All Genders
Healthy Volunteers
ID07215884

Dopamine and Sensorimotor Function in Stuttering

Led by University of California, San Francisco · Updated on 2025-10-14

40

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

U

University of California, San Francisco

Lead Sponsor

N

National Institute on Deafness and Other Communication Disorders (NIDCD)

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are studying the effects of aripiprazole, a drug that affects dopamine, on adults who stutter. Stuttering is a speech disorder that affects fluency, and this study aims to better understand the sensorimotor pathways involved in stuttering and explore possible treatments. The study focuses on how fluency may improve through auditory feedback changes or drugs that regulate dopamine uptake. Participants will receive a single oral dose of 10 mg aripiprazole or a placebo. The study is randomized and triple-blinded, meaning neither participants nor administrators know which treatment is given. This dose is investigational for stuttering and differs from typical uses of aripiprazole, which is approved for other mental health conditions. During the study, participants will be assessed 3 to 4 hours after taking the dose for changes in speech-related brain activity and auditory processing, such as pre-speech auditory modulation and feedback alterations. Researchers will measure these outcomes to understand how aripiprazole affects speech fluency and sensorimotor function. The study is sponsored by the University of California, San Francisco and includes healthy adults aged 18 to 65 who stutter.

CONDITIONS

Brief Title

Dopamine and Sensorimotor Function in Stuttering

Who Can Participate

Age: 18Years - 65Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Native speakers of American English
  • Adults aged 18 to 65 years
  • Presence of stuttering with onset before age 6 years
  • Normal hearing
  • Healthy adults without hearing or language difficulties
Not Eligible

You will not qualify if you...

  • Speech-language-hearing difficulties other than stuttering
  • Neurological or psychological problems
  • Current use of medications affecting the dopaminergic system or benzodiazepines

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Treatment

Duration - 3 to 4 hours after each dose

Participants receive a single dose of aripiprazole or placebo, and effects on speech and sensorimotor function are assessed.

1 visit per dose (in-person)

Trial Site Locations

Total: 1 location

1

Biomagentic Imaging Lab

San Francisco, California, United States, 94143

Actively Recruiting

Loading map...

Research Team

N

Natalie Brunwin, MS

How is the study designed?

Study Type

INTERVENTIONAL

Masking

TRIPLE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

BASIC_SCIENCE

Number of Arms

2

Similar Trials

Information Processing Biases in Adults Who Stutter: Behavio...

Stuttering, Adult

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here

Published Research Related To This Trial

No negative symptoms in healthy volunteers after single doses of amisulpride, aripiprazole, and haloperidol: a double-blind placebo-controlled trial.

Chul-Hyun Park, Tae-Won Park, Jong-Chul Yang...

https://pubmed.ncbi.nlm.nih.gov/22241281

Long-Term Improvement and Safety of Aripiprazole for Irritability and Adaptive Function in Asian Children and Adolescents with Autistic Disorder: A 52-Week, Multinational, Multicenter, Open-Label Study.

Byoung-Uk Kim, Hyo-Won Kim, Eun Jin Park...

https://pubmed.ncbi.nlm.nih.gov/36112116