Study of Neurophysiological Correlates of the Link Between Perception and Action

NCT ID: NCT02851121

Last Updated: 2024-04-22

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

228 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-03-16

Study Completion Date

2024-03-16

Brief Summary

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The main goal of this study is to better understand the link between motor system (action) and perception in variable sensorial forms by examining the time course and the dynamic of electroencephalography (EEG) activations. To do so, differents sensimotor study protocols in linguistics and in the fiels of emotional and spatial perception will be realised in order to study prcisely differents links parception-action.

Detailed Description

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Conditions

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Healthy Volunteer

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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Healthy volunteers

Group Type OTHER

Sensorial stimulations

Intervention Type OTHER

Experimental protocols

Intervention Type OTHER

Emotional protocols

Intervention Type BEHAVIORAL

Protocol with a spatial dimension

Intervention Type OTHER

Interventions

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Sensorial stimulations

Intervention Type OTHER

Experimental protocols

Intervention Type OTHER

Emotional protocols

Intervention Type BEHAVIORAL

Protocol with a spatial dimension

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Signed free consent
* Medical exam done before participation to the study
* Age between 18 and 65 years
* Baccalaureate as minimum degree level

Exclusion Criteria

* Subject already taking part in an other clinical and/or therapeutic trial still in progress
* Important audition or visual disorder
* Language disorders (aphasia, dysphasia, dysarthria, stammer, etc)
* Any counter-argument to MRI
* Pregnant, parturient or brest feeding women. A pregnancy test (urinary) will be offered to female participants during the inclusion medical interview. In the event of a refusal the woman will have to sign a discharge attesting that she doesn't take any risk of getting pregnant and to volunteer to participate to the trial without having recourse to the offered prgnancy test.
* Patient derpived of liberty by a judicial or administrative decision
* Patient under 18 years under a legal protection or unable to express their consent
* Alcohol ingested
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University Hospital, Grenoble

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Laurent Verceuil, Doctor

Role: PRINCIPAL_INVESTIGATOR

Grenoble Hospital University

Locations

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UniversityHospitalGrenoble

La Tronche, , France

Site Status

Countries

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France

References

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Other Identifiers

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38RC14.420

Identifier Type: -

Identifier Source: org_study_id

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