Study of Neurophysiological Correlates of the Link Between Perception and Action (PSM_EEG)

April 18, 2024 updated by: University Hospital, Grenoble

Study of Neurophysiological Correlates of the Link Between Perception and Action Through Varied Protocols of Sensorimotor Studies

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.

Study Overview

Study Type

Interventional

Enrollment (Actual)

228

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

      • La Tronche, France, 38700
        • UniversityHospitalGrenoble

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Other: Healthy volunteers

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Electroencephalography (EEG)
Time Frame: 20 minutes
Software : Brain Analyzer. Hz
20 minutes
Electrooculography (EOG)
Time Frame: Half an hour
mV
Half an hour
Electromyography EMG
Time Frame: Half an hour
EMG Delsys sans fil Trigno Digital system. mV
Half an hour
Electrodermal conductance
Time Frame: Half an hour
EDA device from BrainProduct society. Constant voltage of 0,5V
Half an hour
Anatomical MRI
Time Frame: 15 minutes
15 minutes

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Laurent Verceuil, Doctor, Grenoble Hospital University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 16, 2015

Primary Completion (Actual)

March 16, 2024

Study Completion (Actual)

March 16, 2024

Study Registration Dates

First Submitted

July 27, 2016

First Submitted That Met QC Criteria

July 27, 2016

First Posted (Estimated)

August 1, 2016

Study Record Updates

Last Update Posted (Actual)

April 22, 2024

Last Update Submitted That Met QC Criteria

April 18, 2024

Last Verified

April 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 38RC14.420

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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