- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05675852
Evaluation of Visual Parameters by Visual Evoked Potentials Captured by EEG
Evaluation of Visual Parameters in Healthy and Visually Impaired Adults Using the Sweep and Oddball Technique Associated With Visual Evoked Potentials Captured by EEG
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Contact
- Name: Demet Yuksel
- Phone Number: +32 (2) 764 21 48
- Email: demet.yuksel@saintluc.uclouvain.be
Study Contact Backup
- Name: Coralie Hemptinne
- Phone Number: +32 (2) 764 1969
- Email: coralie.hemptinne@saintluc.uclouvain.be
Study Locations
-
-
Bruxelles
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Woluwe-Saint-Lambert, Bruxelles, Belgium, 1200
- Recruiting
- Institute of Neurosciences
-
Contact:
- Coralie Hemptinne, MD, PhD
- Phone Number: +32 (2) 764 1968
- Email: coralie.hemptinne@saintluc.uclouvain.be
-
Contact:
- Nathan Hupin, MD
- Phone Number: +32 495191707
- Email: nathan.hupin@student.uclouvain.be
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Absence of ocular pathologies except for refractive errors
- Absence of neurologic conditions
Exclusion Criteria:
- Participants using neurologic or psychiatric drugs
- Scalp pathology
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Healthy participants
Healthy participants aged from 1 to 75 years old. All experiments conducted in this study will make use of the electroencephalogram (EEG) recording technique. Healthy participants cannot participate if they suffer from dermatosis on the scalp. There is no other contraindication to the practice of an EEG, which simply consists of recording the electrical activity of the brain on a trace, after application of a conductive gel on the scalp where sensors connected to a recording device are placed. We will collect the cerebral electrical response by the technique of steady state visual evoked potentials (SSVEP) which consists of presenting a visual stimulus periodically to interpret the EEG signal according to those variations. |
Electroencephalography is registered through a 68-electrode electroencephalography while stimuli will be presented at the centre of the screen at a distance of 150cm. The pattern of visual stimulation is based on the technique of steady state visual evoked potentials. These potentials consist of the presentation of a visual stimulus at a (relatively fast) periodic rate to produce an EEG signal over the occipital cortex exactly at the frequency of stimulation. By varying the value of a parameter of the stimulation (e.g. the contrast of the stimulus) varies. This variation makes it possible to determine the threshold value where an EEG response is perceived, and thus to evaluate visual parameters such as visual acuity, contrast sensitivity or recognition of more complex shapes. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Threshold of visual recognition of low and high grade visual stimuli
Time Frame: 4 months
|
Fast periodic visual stimulation using stimuli such as gratings, checkerboards, words and faces
|
4 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 2017%244
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
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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