NCT04818268

Brief Summary

The proposed studies focus on memory for speech movements and sounds and its relation to learning. Continuous theta-burst transcranial magnetic stimulation (cTBS) will be used to suppress activity in a region of pre-frontal cortex associated with somatic and auditory working memory (Brodmann area 46v) to test its involvement in learning.

Trial Health

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Trial Health Score

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

Enrollment
120

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Aug 2019

Longer than P75 for not_applicable

Geographic Reach
1 country

1 active site

Status
terminated

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

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

August 1, 2019

Completed
1.6 years until next milestone

First Submitted

Initial submission to the registry

March 19, 2021

Completed
7 days until next milestone

First Posted

Study publicly available on registry

March 26, 2021

Completed
4.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 31, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 31, 2025

Completed
Last Updated

December 11, 2025

Status Verified

December 1, 2025

Enrollment Period

6 years

First QC Date

March 19, 2021

Last Update Submit

December 5, 2025

Conditions

Outcome Measures

Primary Outcomes (2)

  • Speech Motor Learning

    Learning is assessed on a 0 to 100 scale as change in speech sounds (speech formant frequencies). A score of 100 corresponds to complete adaptation.

    Performance as measured at the end of learning (single day experiment)

  • Sensory Memory

    Sensory Memory is measured on a 0 to 100 scale. A score of 100 corresponds to perfect memory.

    Single day experiment

Study Arms (5)

Adaptation to Altered Auditory Feedback

EXPERIMENTAL

Adaptation to Altered Auditory Feedback

Behavioral: Adaptation

Auditory Sensory Memory

EXPERIMENTAL

Auditory Sensory Memory

Behavioral: Adaptation

Somatosensory Sensory Memory

EXPERIMENTAL

Somatosensory Sensory Memory

Behavioral: Adaptation

Adaptation to Altered Auditory Feedback + cTBS to 46v

EXPERIMENTAL

Adaptation to Altered Auditory Feedback + cTBS to 46v

Behavioral: AdaptationOther: cTBS

Sensory Memory + cTBS to 46v

EXPERIMENTAL

Sensory Memory + cTBS to 46v

Behavioral: AdaptationOther: cTBS

Interventions

AdaptationBEHAVIORAL

Sensorimotor adaptation in speech

Adaptation to Altered Auditory FeedbackAdaptation to Altered Auditory Feedback + cTBS to 46vAuditory Sensory MemorySensory Memory + cTBS to 46vSomatosensory Sensory Memory
cTBSOTHER

continuous theta-burst stimulation

Adaptation to Altered Auditory Feedback + cTBS to 46vSensory Memory + cTBS to 46v

Eligibility Criteria

Age21 Years - 40 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • right handed adults
  • no known physical or neurological abnormalities

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

McGill University

Montreal, Quebec, H3A1G1, Canada

Location

MeSH Terms

Conditions

Speech

Interventions

Acclimatization

Condition Hierarchy (Ancestors)

Verbal BehaviorCommunicationBehavior

Intervention Hierarchy (Ancestors)

Adaptation, PhysiologicalPhysiological PhenomenaAdaptation, BiologicalBiological Phenomena

Study Officials

  • David Ostry

    Haskins Laboratories

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 19, 2021

First Posted

March 26, 2021

Study Start

August 1, 2019

Primary Completion

July 31, 2025

Study Completion

July 31, 2025

Last Updated

December 11, 2025

Record last verified: 2025-12

Data Sharing

IPD Sharing
Will not share

Locations