Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07215884

Dopamine and Sensorimotor Function in Stuttering

Status
Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
University of California, San Francisco · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

This study is being done to understand the effect of aripiprazole on adults who stutter. Stuttering is a disorder that affects speech fluency. This study aims to understand sensorimotor pathways of stuttering and possible interventions.

Detailed description

Stuttering is a disorder of speech fluency that affects 3.5 million people in the USA alone. The goal of this project is to assess whether fluency ehnancement with auditory feedback manipulations or with pharmacological agents that regulate dopamine uptake improve the sensorimotor functions of speech feedback prediction and processing in stuttering. This study may lay the foundation for stuttering treatments that combine dopamine regulators and behavioral treatments. Aripiprazole is an FDA-approved anti-psychotic typically used for treatment of schizophrenia or acute manic episodes. A typical dose is 10-15 mg per day, given daily for treatment. In this study, one 10 mg dose will be given. The usage in this study is purely investigational (experimental) and not FDA approved.

Conditions

Interventions

TypeNameDescription
DRUGAripiprazole 10 MGThe effects of aripiprazole on stuttering and various behavioral and neural outcomes will be studied compared to placebo.
DRUGPlaceboPlacebo will be compared against aripiprazole for effect on stuttering and various behavioral and neural markers.

Timeline

Start date
2025-09-30
Primary completion
2026-06-30
Completion
2026-06-30
First posted
2025-10-14
Last updated
2025-10-14

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT07215884. Inclusion in this directory is not an endorsement.