- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04325971
Study of Eye Movements as Markers of the Physiological, Cerebral and Cognitive State of Healthy Subjects (EyeProxy)
Study Overview
Detailed Description
Cerebral activation following visual stimulation is explored using two neuroimaging techniques EEG and MRI while eye movements are recorded. Three experiments are performed: in MR scanner 1) functional localisation of specific areas: LOC, FFA, MT/V5, V1 and V2 and 2) a saccadic choice experiment; with EEG, replication of the experiments performed in the MR scanner and 3) an additional experiment of movement detection during the ocular saccades.
Thirty young volunteers (18-40 y old) are involved.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Grenoble, France, 38043
- CHU Grenoble Alpes
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Normal vision or corrected to normal
- Social security affiliation
- Signed consent to participate
- No pregnancy fo women
Exclusion Criteria:
- Audition and motor troubles
- Incapable to decide (Persons mentioned in L1121-5,6 et 8 of public health code)
- Neurological disorders
- Pathology affecting oculomotor control
- MRI incompatibility
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: Healthy Subjects
All healthy subject are gathered in one arm
|
MR, EEG recordings
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Eye movement brain networks
Time Frame: 24 months
|
Identification of the cerebral locus of ocular movement via MRI & EEG
|
24 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
OculoDB
Time Frame: 24 months
|
Database repository of healthy population
|
24 months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Sara MEONI, PH, University Hospital, Grenoble
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 (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 38RC20.063
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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