Study of Neurophysiological Correlates of the Link Between Perception and Action

Healthy Volunteer Clinical Trial

— PSM_EEG  

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02851121
• Other study ID #: 38RC14.420
• Status: Completed
• Phase: N/A
• Start date: March 16, 2015
• Est. completion date: March 16, 2024

Study information

• Verified date: April 2024
• Source: University Hospital, Grenoble
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 228
• Est. completion date: March 16, 2024
• Est. primary completion date: March 16, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 65 Years

Eligibility

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

Related Conditions & MeSH terms

• Healthy Volunteer

Intervention

Other:
• Sensorial stimulations

• Experimental protocols

Behavioral:
• Emotional protocols

Other:
• Protocol with a spatial dimension

Locations

Country	Name	City	State
France	UniversityHospitalGrenoble	La Tronche

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Grenoble

Country where clinical trial is conducted

France, 

References & Publications (45)

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* Note: There are 45 references in all — Click here to view all references

Outcome

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