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Speech Motor Learning and Retention (Master Protocol)

Sensorimotor Basis of Speech Motor Learning and Retention

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06467292
Enrollment
330
Registered
2024-06-21
Start date
2024-10-01
Completion date
2029-05-31
Last updated
2026-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Speech

Keywords

Speech Motor Learning, Retention

Brief summary

The overall goal of this research is to test a new model of speech motor learning, whose central hypothesis is that learning and retention are associated with plasticity not only in motor areas of the brain but in auditory and somatosensory regions as well.

Detailed description

Aim 1 involves tests of speech motor memory retention following disruption of left hemisphere brain activity in either auditory, somatosensory or motor cortex or to a control site (hand area motor cortex right hemisphere). Continuous theta-burst stimulation (cTBS) is delivered following adaptation to altered auditory feedback to assess its effects on the retention of new learning. Aim 2 assesses the temporal order in which plasticity occurs in cortical motor and sensory brain areas during speech motor learning. In Aim 3, resting-state fMRI will be interleaved with speech motor adaptation. For information specific to each aim, please refer to the below corresponding, separate, clinicaltrials.gov records: unique IDs: 2000037622\_a for Aim 1, 2000037622\_b for Aim 2 and 2000037622\_c for Aim 3.

Interventions

cTBS stimulation will be applied to different areas of the brain following learning. Stimulation will take place following learning in order to block motor memory retention.

BEHAVIORALAdaptation

Auditory adaptation in speech

DEVICESingle pulse Transcranial magnetic stimulation (TMS)

TMS will be delivered 10 times in each motor evoked potentials (MEP) recording block.

DEVICEfMRI

To assess functional connectivity patterns between regions that predict learning.

Sponsors

Yale University
Lead SponsorOTHER
National Institute on Deafness and Other Communication Disorders (NIDCD)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

Healthy right-handed adults with normal hearing will be recruited in equal number from both sexes. All participants will be fluent English speakers.

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Fluent English speakers * Right-handed * Normal hearing * No speech disorder or reading disability

Exclusion criteria

* 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

Design outcomes

Primary

MeasureTime frameDescription
Speech motor learningPerformance as measured at the end of learning (30 minute session)Audapter software will be used to alter the first and second formant frequencies of the spoken words and this is played back to subjects through headphones. Subjects will be tested both with unaltered feedback and with abruptly introduced frequency shifts.The change in the first (F1) and second format frequency (F2) values will be assessed using Praat.
Retention of learning24 hours after learning (re-test lasts 30 minutes)The retention of adaptation to altered auditory feedback (and relearning) will be quantified in terms of F1 and F2 frequency shifts (relative to pre-training baseline). Larger values indicate more complete relearning or retention.

Countries

United States

Contacts

CONTACTMichael Stern
michael.stern@yale.edu2038656163
PRINCIPAL_INVESTIGATORDavid Ostry

Yale University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 19, 2026