Actively Recruiting

Phase Not Applicable
Age: 18Years - 40Years
All Genders
Healthy Volunteers
ID06467305

Sensorimotor Basis of Speech Motor Learning and Retention

Led by Yale University · Updated on 2026-02-19

160

Participants Needed

1

Research Sites

26 weeks

Total Duration

On this page

Sponsors

Y

Yale University

Lead Sponsor

N

National Institute on Deafness and Other Communication Disorders (NIDCD)

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to understand how the brain learns and retains new speech movements by studying brain plasticity not only in motor areas but also in auditory and sensory regions. The central idea is that changes in these brain areas help with learning and holding onto new speech patterns. The study tests this by disrupting activity in specific brain regions using transcranial magnetic stimulation (TMS) and observing how this affects speech motor learning and retention. Participants will read sentences aloud while hearing their voice altered through headphones to induce speech motor adaptation. After this learning phase, a specific type of brain stimulation called continuous theta-burst stimulation (cTBS) is applied to either the auditory, somatosensory, or motor cortex of the left hemisphere, or a control area in the right hemisphere. The treatment is delivered following the learning task, and participants return 24 hours later to assess how well they retained the new speech motor learning. Both altered and unaltered auditory feedback conditions are included to test specific effects of the brain stimulation. During the study, participants perform learning tasks over two days, with cTBS applied after the second day’s task. Researchers measure performance at the end of learning and retention after 24 hours, each lasting about 30 minutes. The study includes brain imaging and evoked potential recordings to identify brain regions involved in learning and retention. Participants are monitored for changes in speech motor performance and brain activity throughout the process.

CONDITIONS

Brief Title

Speech Motor Learning and Retention (Aim 1)

Who Can Participate

Age: 18Years - 40Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Fluent English speakers
  • Right-handed
  • Normal hearing
  • No speech disorder or reading disability
  • Age between 18 and 40 years
Not Eligible

You will not qualify if you...

  • Cardiac pacemaker
  • Aneurysm clip
  • Heart or vascular clip
  • Prosthetic valve
  • Metal implants
  • Metal in brain, skull, or spinal cord
  • Implanted neurostimulator
  • Medication infusion device
  • Cochlear implant or tinnitus (ringing in ears)
  • Personal and/or family history of epilepsy or other neurological disorders or history of head concussion
  • Psychoactive medications
  • Pregnancy

AI-Screening

AI-Powered Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Adaptation

Duration - 2 days

Participants perform learning tasks involving reading sentences aloud while receiving altered or unaltered auditory feedback. This occurs on two consecutive days with brain stimulation applied following learning.

2 visits (in-person)

Implementation

Duration - Occurs immediately after each learning session on 2 days

Participants receive continuous theta-burst stimulation (cTBS) applied to specific brain regions immediately following the learning tasks to study effects on speech motor learning and retention.

2 visits (in-person, concurrent with Adaptation visits)

Retention Assessment

Duration - 30 minutes per visit, repeated after each learning day

Participants return approximately 24 hours after the learning sessions to assess retention of speech motor learning.

2 visits (in-person, 24 hours after each Adaptation visit)

Trial Site Locations

Total: 1 location

1

Yale Child Study Center

New Haven, Connecticut, United States, 06520

Actively Recruiting

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Research Team

D

David Ostry

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

BASIC_SCIENCE

Number of Arms

8

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