- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03929289
The Visuo-attentional Mediator of Social Facilitation (VAMOS)
Social psychology has long established that the mere presence of others influences the investigator's individual behavior and performance. "Social facilitation" refers to any improvement or deterioration of performance due to the presence of others. For more than a century, social psychology has acquired a solid knowledge of the principles governing this fundamental form of social influence.
But the underlying mechanism of social facilitation remains debated, as behavior alone cannot identify it with certainty. This major unresolved problem makes it particularly difficult to translate laboratory results on social facilitation into real applications in areas such as school or work, where others are ubiquitous. The purpose of this study will therefore be to identify the mediator of social facilitation.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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-
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Bron, France, 69500
- Centre de Recherche en Neuroscience de Lyon
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Male or female
- Aged 18 to 35 years old
- Signed written informed consent
- Insurance coverage
Exclusion Criteria:
- Neurological or psychiatric or ophthalmological disorder
- Non-stabilized medical condition
Ongoing treatment with drugs that affect the central nervous system
- Uncorrected visual inadequacy
- No fluency in French reading
- Pregnant and / or breastfeeding woman, this exclusion criterion will be sought by questioning the subject
- Subject commonly in care in a health or social facility for purposes other than that of research
- Subject under guardianship
- Subject deprived of liberty by a judicial or administrative decision
- Incompatibility with the Magnetic Resonance Imaging (MRI) examination determined by answering the following questions:
- Carrier of a neurological stimulator, cardiac (battery) or defibrillator
- Carrier of a cardiac prosthesis (valve, stent ...) or vascular
- Holder of intracranial clips or clamps (staples)
- Carrier of a cerebrospinal fluid bypass
- Presence of metal chips in the eyes
- Metal prosthesis carrier (teeth, knees)
- Pump carrier or infusion system
- Presence of metal tattoo near the head
- Presence of permanent makeup
- Claustrophobia or respiratory disorders
Study Plan
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 |
|---|---|
|
Experimental: Social Facilitation
Cognitive tasks during the 2 functional Magnetic Resonance Imaging (fMRI) observed or not by a subject's known peer.
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During the functional Magnetic Resonance Imaging (fMRI) scans, the subject will perform cognitive tasks measuring eye movements and attention alternatively observed by a familiar peer (in an adjacent room) or not.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Brain activation
Time Frame: 50 minutes
|
Cerebral Blood Oxygenation Level-Dependent (BOLD) signals
|
50 minutes
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Behavioral performances
Time Frame: 50 minutes
|
pupillary diameter
|
50 minutes
|
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Behavioral performances
Time Frame: 50 minutes
|
error rate
|
50 minutes
|
|
Behavioral performances
Time Frame: 50 minutes
|
reaction time
|
50 minutes
|
|
Behavioral performances
Time Frame: 50 minutes
|
oculomotor kinematic parameters: velocity of saccades.
|
50 minutes
|
|
Behavioral performances
Time Frame: 50 minutes
|
oculomotor kinematic parameters: duration of saccades.
|
50 minutes
|
|
Behavioral performances
Time Frame: 50 minutes
|
oculomotor kinematic parameters: precision of saccades.
|
50 minutes
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Denis PELISSON, Centre de Recherche en Neuroscience de Lyon
Publications and helpful links
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 69HCL19_0268
- 2019-A01027-50 (Other Identifier: ID-RCB)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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