NCT07459803

Brief Summary

This study aims to understand how people use different types of feedback to control their speech. When an individual speaks, the brain relies on several systems at the same time, such as sensory systems that monitor an individuals own voice and the movements of their speech muscles, and a motor system that builds and reads out learned motor patterns. The investigators are studying how these systems work together and how they differ across individuals. Investigators will test 90 adults between 18 and 50 years old, including people who stutter, people with dyslexia, and people with typical speech and reading development. Participants will complete several short speech tasks in which the sounds they hear or the movements of their jaw or larynx are briefly changed. These responses will be used to measure each person's speech motor skills and to estimate the settings of a computer model called "SimpleDIVA," which simulates how the brain controls speech. Participants will also complete an MRI scan so investigators can measure the structure and connectivity of different brain regions. These measures will help investigators understand how individual differences in the brain relate to the speech motor control skills we observe. Participants will also complete sessions with noninvasive brain stimulation (transcranial current stimulation, or tCS) to examine how stimulation of specific areas of the brain affects responses during the speech tasks. The knowledge gained from this study will help researchers understand why speech motor skills vary across people and how differences in neural function may contribute to conditions such as stuttering and dyslexia.

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
90

participants targeted

Target at P50-P75 for not_applicable

Timeline
43mo left

Started Jun 2026

Longer than P75 for not_applicable

Geographic Reach
1 country

2 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress4%
Jun 2026Mar 2030

First Submitted

Initial submission to the registry

December 12, 2025

Completed
3 months until next milestone

First Posted

Study publicly available on registry

March 10, 2026

Completed
3 months until next milestone

Study Start

First participant enrolled

June 12, 2026

Completed
3.7 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2030

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2030

Last Updated

July 21, 2026

Status Verified

July 1, 2026

Enrollment Period

3.7 years

First QC Date

December 12, 2025

Last Update Submit

July 20, 2026

Conditions

Keywords

Stuttering DevelopmentalMagnetic Resonance ImagingSpeech Motor LearningSpeech DisordersNeurocomputational ModelingDyslexia

Outcome Measures

Primary Outcomes (2)

  • Reflexive compensatory response

    The amount of compensation to induced F0 and F1 perturbations will be calculated by finding the maximum deviation of the perturbed variable (F0 or F1) from baseline, dividing it by the perturbation size, and then averaging that across all trials of that perturbation.

    Day 1 and Day 2

  • Adaptive compensatory response

    The adaptive compensatory response to persistent F0 and F1 perturbations will be calculated by subtracting the mean F0/F1 from the baseline phase from the mean during the after-effect phase, then dividing by the perturbation size to obtain percent adaptation.

    Day 1 and Day 2

Secondary Outcomes (10)

  • Stuttering Severity

    Baseline

  • Dyslexia Severity

    Baseline

  • Verbal and Nonverbal Intelligence

    Baseline

  • Receptive Vocabulary

    Baseline

  • Brain region volume

    Day 2

  • +5 more secondary outcomes

Study Arms (2)

pSTG and vSSC tCS Targeting

EXPERIMENTAL

Participants in Arm 1 will complete all behavioral, MRI, and tCS study procedures. During the tCS portion of the study, they will receive anodal transcranial current stimulation (tCS) targeting two brain regions: posterior superior temporal gyrus (pSTG) in one stimulation session and ventral somatosensory cortex (vSSC) in another. In a third session, they will complete the same speech task while receiving sham stimulation targeting either pSTG or vSSC. All participants in this arm will also complete speech motor control tasks involving unpredictable auditory perturbations, sustained auditory perturbations, and somatosensory perturbations, as well as one MRI session.

Behavioral: Unpredictable auditory feedback perturbation: 2 behavioral sessionsBehavioral: Unpredictable auditory feedback perturbation during tCS: 3 behavioral sessionsBehavioral: Sustained F1 auditory feedback perturbationBehavioral: Sustained F0 auditory feedback perturbationBehavioral: Reflexive somatosensory perturbationOther: Anodal tCS targeting pSTG and vSSCOther: Sham tCS targeting pSTG or vSSC

Left and Right vPMC tCS Targeting

EXPERIMENTAL

Participants in Arm 2 will complete all behavioral, MRI, and tCS study procedures. During the tCS portion of the study, they will receive anodal transcranial current stimulation (tCS) targeting left ventral premotor cortex (vPMC) in one stimulation session and right vPMC in another. In a third session, they will complete the same speech task while receiving sham stimulation targeting either the left or right vPMC. All participants in this arm will also complete speech motor control tasks involving unpredictable auditory perturbations, sustained auditory perturbations, and somatosensory perturbations, as well as one MRI session.

Behavioral: Unpredictable auditory feedback perturbation: 2 behavioral sessionsBehavioral: Unpredictable auditory feedback perturbation during tCS: 3 behavioral sessionsBehavioral: Sustained F1 auditory feedback perturbationBehavioral: Sustained F0 auditory feedback perturbationBehavioral: Reflexive somatosensory perturbationOther: Anodal tCS targeting left or right vPMCOther: Sham tCS targeting left vPMC or right vPMC

Interventions

Participants in Arms 1 and 2 will repeat consonant/vowel/consonant (/CVC/) words containing the vowel "eh" between two consonants that they hear over headphones. As they speak, vocal output from the participant will be transduced via a microphone and then played back to the participant over headphones at an undetectable delay. On a subset of (perturbed) trials, F0 or F1 in the auditory feedback presented to the participant will be shifted relative to their vocal output. On the remaining (baseline) trials, auditory feedback will be unaltered. During each behavioral session, participants will complete 80 unperturbed trials, 40 trials that involve an F0 perturbation, and 40 trials that involve an F1 perturbation.

Left and Right vPMC tCS TargetingpSTG and vSSC tCS Targeting

Participants in Arms 1 and 2 will repeat /CVC/ words containing the vowel "eh" between two consonants that they hear over headphones. As they speak, vocal output from the participant will be transduced via a microphone and then played back to the participant over headphones at an undetectable delay. On a subset of (perturbed) trials, F0 or F1 in the auditory feedback presented to the participant will be shifted relative to their vocal output. On the remaining (baseline) trials, auditory feedback will be unaltered. During each session, participants will complete 50 unperturbed trials, 50 trials that involve an F0 perturbation, and 50 trials that involve an F1 perturbation.

Left and Right vPMC tCS TargetingpSTG and vSSC tCS Targeting

Participants in Arms 1 and 2 will repeat /CVC/ words containing the vowel "eh" between two consonants that they hear over headphones. As they speak, vocal output from the participant will be transduced via a microphone and then played back to the participant over headphones at an undetectable delay. Over the course of each protocol, the first formant (F1) in the auditory feedback presented to the participant will be shifted relative to their vocal output. Trials will be organized in four phases: an initial baseline phase in which auditory feedback is unaltered, a ramp phase over which the formant of auditory feedback is gradually shifted to a maximum level, a hold phase in which the feedback shift is held at its maximum level, and then an after-effect phase in which feedback returns to normal. Four trials will be performed in each phase.

Left and Right vPMC tCS TargetingpSTG and vSSC tCS Targeting

Participants in Arm 1 and 2 will repeat /CVC/ words containing the vowel "eh" between two consonants that they hear over headphones. As they speak, vocal output from the participant will be transduced via a microphone and then played back to the participant over headphones at an undetectable delay. As they speak the fundamental frequency (F0) in the auditory feedback presented to the participant will be shifted relative to their vocal output. Trials will be organized in four phases: an initial baseline phase in which auditory feedback is unaltered, a ramp phase over which the formant of auditory feedback is gradually shifted to a maximum level, a hold phase in which the feedback shift is held at its maximum level, and then an after-effect phase in which feedback returns to normal.

Left and Right vPMC tCS TargetingpSTG and vSSC tCS Targeting

Participants in Arms 1 and 2 will repeat /CVC/ words containing the vowel "eh" between two consonants that they hear over headphones. While they speak, speech-shaped masking noise will be presented to participants at 85 dB. On a subset of trials (word productions), movements of the jaw will be perturbed (restricted) by the rapid inflation of a balloon placed between the upper and lower teeth shortly after voice onset. On another subset of trials, the position of the larynx will be perturbed by the rapid inflation of a balloon placed against the laryngeal prominence. During the remaining (unperturbed) trials, both balloons will remain deflated.

Left and Right vPMC tCS TargetingpSTG and vSSC tCS Targeting

Participants in Arm 1 will receive continuous anodal tCS targeting posterior superior temporal gyrus (pSTG) during a 20-minute reflexive auditory feedback task during one session and stimulation targeting ventral somatosensory cortex (vSSC) during the same task in another session. The tCS stimulation will ramp up to its maximum value (2 milliamperes) over the first 30 s of the session and will be maintained at that level throughout the remainder of the session.

pSTG and vSSC tCS Targeting

Participants in Arm 2 will receive continuous anodal tCS targeting left ventral premotor cortex (vPMC) during a 20-minute reflexive auditory feedback task during one session and stimulation targeting right vPMC during the same task in another session. The tCS stimulation will ramp up to its maximum value (2 milliamperes) over the first 30 s of the session and will be maintained at that level throughout the remainder of the session.

Left and Right vPMC tCS Targeting

Participants in Arm 1 will receive Sham tCS stimulation targeting the pSTG or vSSC during a 20-minute reflexive auditory feedback task. During the minute prior to training onset, the tCS stimulator will ramp up to 2 milliamperes and then back down to 0 for the remainder of the session.

pSTG and vSSC tCS Targeting

Participants in Arm 1 will receive Sham tCS stimulation targeting left or right vPMC during a 20-minute reflexive auditory feedback task. During the minute prior to training onset, the tCS stimulator will ramp up to 2 milliamperes and then back down to 0 for the remainder of the session.

Left and Right vPMC tCS Targeting

Eligibility Criteria

Age18 Years - 50 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Native speakers of American English
  • Adults age 18-50
  • Age-appropriate cognitive and receptive vocabulary skills
  • Age-appropriate hearing
  • Adults with dyslexia will have a history of dyslexia or report of ongoing reading difficulties that will be confirmed at the first screening visit
  • Adults who stutter will have a history of stuttering that will be confirmed at the first screening visit

You may not qualify if:

  • History of neurological disorder, including a history of seizures
  • Major brain injury, brain surgery, or stroke
  • Orthodontia or atypical oral structure (e.g., cleft palate) that interferes with speech
  • Fluency disorder (except those in the persons who stutter cohort), apraxia of speech, or dysarthria
  • Language or reading disorder (except those in persons with dyslexia cohort)
  • Standardized score below 80 on the Kaufman Brief Intelligence Test
  • Standardized score below 1 standard deviation on the NIH Toolbox Picture Vocabulary Test
  • Pregnancy
  • Severe claustrophobia
  • Presence of magnetically or mechanically active implant, or other ferromagnetic material embedded in any part of the body
  • Significant scalp lesions that would prevent transcranial direct stimulation

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Boston University Charles River Campus

Boston, Massachusetts, 02115, United States

RECRUITING

Boston University

Boston, Massachusetts, 02215, United States

RECRUITING

MeSH Terms

Conditions

StutteringDyslexiaSpeech Disorders

Condition Hierarchy (Ancestors)

Language DisordersCommunication DisordersNeurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and SymptomsSpecific Learning DisorderLearning DisabilitiesNeurodevelopmental DisordersMental Disorders

Study Officials

  • Frank H Guenther, Ph.D.

    Boston University

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Frank H Guenther, Ph.D.

CONTACT

Barbara G Holland, M.A.

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

December 12, 2025

First Posted

March 10, 2026

Study Start

June 12, 2026

Primary Completion (Estimated)

March 1, 2030

Study Completion (Estimated)

March 1, 2030

Last Updated

July 21, 2026

Record last verified: 2026-07

Data Sharing

IPD Sharing
Will share

Locations