Multistability: Perception is Inspired by Noise

NCT ID: NCT03723044

Last Updated: 2024-01-17

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 80 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2020-06-05
• Study Completion Date: 2025-05-31

Brief Summary

Some stimuli, such as sinusoidal networks in motion, or the best known, Necker's cube, are simple visual stimulations generating interpretations of unstable and oscillatory shapes or movements, mutually exclusive. Currently, the explanatory models of these perception phenomena are based on adaptation and learning mechanisms as well as the importance of noise in the perceptual and decision-making system. Often noise is a harmful component, but it can also be a facilitator in perceptual systems: the investigator's eye is always in motion, it is the micro-movements during eye fixation (phase of eye stability). In particular, the role of micro-eye movements has been identified in perceptual systems, and it will be necessary here to relate these micro-movements to the perceptive tilts facing multisable stimuli. However, how to access the perceptive states is a real question, since it has been shown that the participant's transfer of his perceptual state by means of a motor response can alter the very state of the percept. This is why the EEG activity will be analyzed to learn to discriminate the different percepts over time, without disruption of the participant's perceptual exploration endogenous activity.

Detailed Description

Each participant will benefit from a medical interview before inclusion to eliminate the contraindications to this study. The maximum duration of the individual participation of each subject in this study is 5 hours in two sessions. Each session lasts 2h30. Both sessions are spaced a maximum of 14 days apart. Each session includes EEG headset placement and oculometer calibration (20 min), followed by recording EEG and eye tracking activity during a visual cognitive task where the participant will be presented with multi-stable visual stimuli to watch. for one or two minutes after the tests. By repeating the essays and the conditions of presentation, each session will be organized in six blocks of 20 minutes each, interspersed with a break.

Conditions

No Conditions

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: NONE

Study Groups

healthy volunteers

Group Type: EXPERIMENTAL

EEG and occulometry

Intervention Type: OTHER

Each participants will spend two sessions of EEG and occulometry during a visual cognitive task where she/her will be presented with multi-stable visual stimuli to gaze at for one or two minutes. Depending on the experimental conditions, the participant will provide or not her/his perceptual state (i.e. which stimulus has been perceived ).

Interventions

EEG and occulometry

Each participants will spend two sessions of EEG and occulometry during a visual cognitive task where she/her will be presented with multi-stable visual stimuli to gaze at for one or two minutes. Depending on the experimental conditions, the participant will provide or not her/his perceptual state (i.e. which stimulus has been perceived ).

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Signed informed consent
• Medical examination carried out before the participation in the research
• Age between 18 and 55 years
• Minimum level of studies
• Obligation to join the social security system
• normal or corrected vision normal

Exclusion Criteria

• Subject included in another clinical and / or therapeutic experimentation in progress
• Major vision disorder
• Past or current neurological or neuropsychiatric pathologies
• History of cranial trauma with loss of consciousness.
• Medication treatments likely to modulate brain activity: benzodiazepine, antidepressants, neuroleptics, lithium, etc.
• Diabetes, cardiac pathology, immunodeficiency.
• Medication treatments likely to modulate the activity of the cardiovascular system.
• History of abuse or recent ingestion of alcohol, hard drugs or doping products.
• Consumption of more than 15 cigarettes per day
• Subject deprived of liberty by a judicial or administrative decision (L1121-6 CSP)
• Major subject subject to a legal protection measure or unable to express their consent (L1121-8 CSP)
• Pregnant, parturient and nursing mothers (L1121-5)

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 55 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

GIPSA-LAB

OTHER

Sponsor Role: collaborator

University Hospital, Grenoble

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

CHU Grenoble-Alpes

Grenoble, , France

Site Status: RECRUITING

Countries

France

Central Contacts

Anne Guerin, PhD

Role: CONTACT

anne.guerin@gipsa-lab.grenoble-inp.fr

4 76 57 43 73 ext. 0033

Tiphaine Montagnon

Role: CONTACT

tmontagnon@chu-grenoble.fr

Facility Contacts

Anne GUERIN

Role: primary

Other Identifiers

38RC18.059

Identifier Type: -

Identifier Source: org_study_id