Study of Visual-spatial Attention by Eye Tracking as a Function of Central or Peripheral Visual Impairment
Not Applicable
Terminated
- Conditions
- Central or Peripheral Visual Impairment
- Interventions
- Procedure: microperimetryProcedure: visual acuityProcedure: automated visual fieldProcedure: eye movements recording
- Registration Number
- NCT03505398
- Lead Sponsor
- Nantes University Hospital
- Brief Summary
The objective of this pilot work is to determine the role of central and peripheral visions in explicit attention processes (saccade planning) in the case of visual impairment.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- TERMINATED
- Sex
- All
- Target Recruitment
- 71
Inclusion Criteria
- Male or female ≥18 years;
- Patient with a central visual deficit (central scotoma on the visual field: DMLA, cones dystrophy ...) or peripheral (annular scotoma: chronic glaucoma, retinitis pigmentosa ...) or without visual deficit (corrected visual acuity and visual field)
- Patient agreeing to participate in the study and signing informed consent
- Patient affiliated to social security
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Exclusion Criteria
- Pregnant woman
- Patient with known epilepsy
- Major under judicial safeguard, or deprived of liberty
- Major under guardianship or curatorship or admitted to a health or social institution for purposes other than research.
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description control eye movements recording - central vision disorder microperimetry - control microperimetry - central vision disorder eye movements recording - peripheral vision disorder visual acuity - central vision disorder visual acuity - central vision disorder automated visual field - peripheral vision disorder automated visual field - peripheral vision disorder microperimetry - peripheral vision disorder eye movements recording - control visual acuity - control automated visual field -
- Primary Outcome Measures
Name Time Method Microperimetry recording (central versus peripheral) Day 0 recording of automated visual field (central versus peripheral) Day 0 Measurement of visual acuity (central versus peripheral) Day 0 recording of eye movements (central versus peripheral) Day 0
- Secondary Outcome Measures
Name Time Method recording of automated visual field (patient versus control) Day 0 Microperimetry recording (patient versus control) Day 0 recording of eye movements (patient versus control) Day 0 Measurement of visual acuity (patient versus control) Day 0
Trial Locations
- Locations (1)
CHU de Nantes
🇫🇷Nantes, France