PSM_EEG: Study of Neurophysiological Correlates of the Link Between Perception and Action

Sponsor
University Hospital, Grenoble (Other)
Overall Status
Recruiting
CT.gov ID
NCT02851121
Collaborator
(none)
250
1
1
108
2.3

Study Details

Study Description

Brief Summary

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.

Condition or Disease Intervention/Treatment Phase
  • Other: Sensorial stimulations
  • Other: Experimental protocols
  • Behavioral: Emotional protocols
  • Other: Protocol with a spatial dimension
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
250 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Study of Neurophysiological Correlates of the Link Between Perception and Action Through Varied Protocols of Sensorimotor Studies
Actual Study Start Date :
Mar 16, 2015
Anticipated Primary Completion Date :
Mar 16, 2024
Anticipated Study Completion Date :
Mar 16, 2024

Arms and Interventions

Arm Intervention/Treatment
Other: Healthy volunteers

Other: Sensorial stimulations

Other: Experimental protocols

Behavioral: Emotional protocols

Other: Protocol with a spatial dimension

Outcome Measures

Primary Outcome Measures

  1. Electroencephalography (EEG) [20 minutes]

    Software : Brain Analyzer. Hz

  2. Electrooculography (EOG) [Half an hour]

    mV

  3. Electromyography EMG [Half an hour]

    EMG Delsys sans fil Trigno Digital system. mV

  4. Electrodermal conductance [Half an hour]

    EDA device from BrainProduct society. Constant voltage of 0,5V

  5. Anatomical MRI [15 minutes]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 UniversityHospitalGrenoble La Tronche France 38700

Sponsors and Collaborators

  • University Hospital, Grenoble

Investigators

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

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
University Hospital, Grenoble
ClinicalTrials.gov Identifier:
NCT02851121
Other Study ID Numbers:
  • 38RC14.420
First Posted:
Aug 1, 2016
Last Update Posted:
May 9, 2022
Last Verified:
May 1, 2022
Keywords provided by University Hospital, Grenoble

Study Results

No Results Posted as of May 9, 2022