Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
NA
120 participants
INTERVENTIONAL
2019-08-01
2025-07-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
BASIC_SCIENCE
NONE
Study Groups
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Adaptation to Altered Auditory Feedback
Adaptation to Altered Auditory Feedback
Adaptation
Sensorimotor adaptation in speech
Auditory Sensory Memory
Auditory Sensory Memory
Adaptation
Sensorimotor adaptation in speech
Somatosensory Sensory Memory
Somatosensory Sensory Memory
Adaptation
Sensorimotor adaptation in speech
Adaptation to Altered Auditory Feedback + cTBS to 46v
Adaptation to Altered Auditory Feedback + cTBS to 46v
Adaptation
Sensorimotor adaptation in speech
cTBS
continuous theta-burst stimulation
Sensory Memory + cTBS to 46v
Sensory Memory + cTBS to 46v
Adaptation
Sensorimotor adaptation in speech
cTBS
continuous theta-burst stimulation
Interventions
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Adaptation
Sensorimotor adaptation in speech
cTBS
continuous theta-burst stimulation
Eligibility Criteria
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Inclusion Criteria
* no known physical or neurological abnormalities
Exclusion Criteria
* 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.
21 Years
40 Years
ALL
Yes
Sponsors
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Yale University
OTHER
National Institute on Deafness and Other Communication Disorders (NIDCD)
NIH
Responsible Party
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Principal Investigators
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David Ostry
Role: PRINCIPAL_INVESTIGATOR
Haskins Laboratories
Locations
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McGill University
Montreal, Quebec, Canada
Countries
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Provided Documents
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Document Type: Informed Consent Form
Other Identifiers
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2000025475_a
Identifier Type: -
Identifier Source: org_study_id
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