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Sensory Basis of Speech Motor Learning

Brain Structures in Speech Motor Memory Consolidation

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04497428
Enrollment
160
Registered
2020-08-04
Start date
2019-08-01
Completion date
2025-07-31
Last updated
2025-12-11

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

Conditions

Speech, Consolidation

Brief summary

These studies test the hypothesis that sensory areas of the brain participate in the consolidation of speech motor memory by using transcranial magnetic stimulation to suppress activity in somatosensory and auditory cortex following adaptation in order to block retention of learning.

Detailed description

Subjects will train using either altered somatosensory feedback or altered auditory feedback (different groups of subjects). Immediately following adaptation, continuous theta burst magnetic stimulation (cTBS) will be applied to either auditory or somatosensory or motor cortex with the goal of blocking consolidation of motor memory. The logic of applying cTBS to both sensory areas is to test the hypothesis that both areas are involved in motor memory consolidation. Subjects leave the laboratory following cTBS and return 24 hours later to assess retention of learning. Learning is assessed as percentage change in speech sounds or movements relative to baseline. Retention is measured on a 0 to 100 scale relative to the end of learning.

Interventions

BEHAVIORALAdaptation

Sensorimotor adaptation in speech

OTHERcTBS

continuous theta-burst stimulation

Sponsors

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

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

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

Inclusion criteria

* right handed adults * no known physical or neurological abnormalities

Exclusion criteria

* patients with: * cardiac pacemaker * surgical clips or values on the heart * implants * metal or metallic fragments in any part of the body * pregnancy * claustrophobia * a personal or family history of epilepsy * currently taking antipsychotic drugs * currently taking antidepressant drugs * currently taking antianxiety drugs * history of concussion.

Design outcomes

Primary

MeasureTime frameDescription
Motor LearningPerformance as measured at the end of learning (30 minute session)Learning is assessed as percentage change in speech sounds (speech formant frequencies) or movements (movement curvature) relative to baseline.
Retention of Learning24 hours after learning (re-test lasts 30 minutes)Retention is measured on a 0 to 100 scale relative to the end of learning.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026