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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04547569
Other study ID # 38RC18.173
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 20, 2020
Est. completion date July 6, 2021

Study information

Verified date May 2022
Source University Hospital, Grenoble
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

These studies test the hypothesis that frontal areas of the brain participate in the cortical networks involved in the somotosensory processing that happens during speech motor learning.


Description:

This work aims to study the role of sensory systems in human motor learning and specifically addresses the involvement of somatosensory cortical networks in motor learning of speech. Previous studies in the literature have highlighted the plasticity of cortical sensory networks, notably the primary and secondary somatosensory cortex and the ventral premotor cortex, during motor learning tasks. The present project focuses on the somatosensory region with connections to the sensorimotor regions of the frontal and parietal cortex. We propose to use neuroimaging (fMRI), in order to verify which areas in the prefrontal cortex are part of the sensorimotor network used in the learning of speech motor tasks in humans. Subjects will be tested in the fMRI scanner while performing either a behavioral task in which the auditory feedback of their own speech is altered or while performing a vibrotactile discrimination task.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date July 6, 2021
Est. primary completion date July 6, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 35 Years
Eligibility Inclusion Criteria: - Right-handed subjects - Subjects fluent in French - Signed informed consent - Affiliation to or beneficiary of a Social Security scheme Exclusion Criteria: - Left-handed subjects - Criteria for contraindications to protocol fMRI scans - Existence of a severe general condition: cardiac, respiratory, hematological, renal, hepatic, cancerous. - Hearing, language (including dyslexia), neurological or psychiatric disorders. - Participation in other ongoing intervention research protocols with exclusionary period or within the previous week - Drug treatment likely to modulate brain activity: benzodiazepines, antidepressants, neuroleptics, lithium, etc. - Protected persons referred to in articles L1121 5 to L1121 8 of the French CSP: - Pregnant women, parturients, nursing mothers, - Persons deprived of liberty by a judicial or administrative decision, - Persons under psychiatric care, - Individuals admitted to a health or social institution for purposes other than research, - Minors, - Persons over the age of majority who are subject to a legal protection measure or who are unable to express their consent

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Speech adaptation
Sensorimotor adaptation in speech
Vibrotactile Discrimination
Vibrotactile Discrimination
Other:
fMRI
fMRI measurement of brain activity
Behavioral:
Speech production
Speech production task

Locations

Country Name City State
France CHU Grenoble-Alpes Grenoble

Sponsors (4)

Lead Sponsor Collaborator
University Hospital, Grenoble GIPSA-LAB, Laboratoire de Psychologie et NeuroCognition, McGill University

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Motor Learning Learning is assessed as percentage change in speech sounds (speech formant frequencies) relative to baseline. Performance as measured at the end of learning (during the 1h30 scanner session)
Primary Brain activity Brain activity are measure by the BOLD signal during both task-based and resting-state blocks 1h30 scanner session
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