NCT05539508

Brief Summary

Despite its low spatial resolution, peripheral vision is very useful for rapidly categorizing a visual scene. Low spatial frequencies of a visual stimulus available in peripheral vision would allow a coarse categorization of the scene and objects (deciding, for example, whether it is an urban or natural landscape). This first representation would then trigger predictive mechanisms which would subsequently guide a more detailed visual analysis in central vision. The psychophysical studies that the investigators have already conducted in this scientific context has been carried out under normal vision conditions. The objective of this project is to study the influence of peripheral vision on central vision with an original approach: What are the consequences of a loss of peripheral vision on the processing performed in central vision? The project will concern patients with glaucoma. This ophthalmic pathology particularly affects the peripheral retina and thus represents a good pathological cognitive model of a visual recognition system in which peripheral vision is less important. The investigators will conduct psychophysical studies with glaucomatous patients and healthy volunteers with normal vision. All participants will be required to perform a short experiment on a computer (15 minutes) where they will look at different photographs of scenes of different luminance and spatial frequencies. Participants will have to perform various tasks on these images using the keys on the keyboard.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
120

participants targeted

Target at P50-P75 for all trials

Timeline
14mo left

Started Oct 2022

Longer than P75 for all trials

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress76%
Oct 2022Jul 2027

First Submitted

Initial submission to the registry

August 23, 2022

Completed
22 days until next milestone

First Posted

Study publicly available on registry

September 14, 2022

Completed
17 days until next milestone

Study Start

First participant enrolled

October 1, 2022

Completed
3.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2026

Expected
1 year until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2027

Last Updated

September 14, 2022

Status Verified

August 1, 2022

Enrollment Period

3.8 years

First QC Date

August 23, 2022

Last Update Submit

September 13, 2022

Conditions

Outcome Measures

Primary Outcomes (2)

  • Psychophysical measure : Percentage of correct response

    Measure calculated by the comparison between the expected response and the response provided by the participant for each trial of the experiment

    Through study completion of 45 months

  • Psychophysical measure : Mean reaction time in milliseconds

    Measure calculated by averaging the time in milliseconds taken by the participant to provide the response for each trial of the experiment

    Through study completion of 45 months

Study Arms (2)

Primary open-angle glaucoma (POAG) group

Behavioral: Psychophysical evaluation

Age-matched normally sighted control group

Behavioral: Psychophysical evaluation

Interventions

All participants will be required to perform a short experiment on a computer (15 minutes) where they will look at different photographs of scenes of different luminance and spatial frequencies. They will have to perform various tasks on these images using the keys on the keyboard.

Age-matched normally sighted control groupPrimary open-angle glaucoma (POAG) group

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

POAG patients and age-matched normally sighted controls

You may qualify if:

  • For patients :
  • between 18 and 80 years old
  • stable bilateral primary open angle glaucoma (POAG)
  • visual acuity \> 5/10 for distant vision for the eye tested
  • peripheral visual field defect on the eye tested measured through a Humphrey Visual Field Analyzer
  • For healthy volunteers :
  • between 18 and 80 years old
  • visual acuity \> 5/10
  • absence of ophthalmologic disease other than Glaucoma (age-related macular degeneration, cataract except for uncomplicated cataract surgery, amblyopia, optic neuropathy, diabetic retinopathy …)

You may not qualify if:

  • ophthalmologic disease other than Glaucoma (age-related macular degeneration, cataract except for uncomplicated cataract surgery, amblyopia, optic neuropathy, diabetic retinopathy …)
  • treated with medication that might compromise sustained attention (benzodiazepine, narcoleptics)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Related Publications (3)

  • Roux-Sibilon A, Rutge F, Aptel F, Attye A, Guyader N, Boucart M, Chiquet C, Peyrin C. Scene and human face recognition in the central vision of patients with glaucoma. PLoS One. 2018 Feb 26;13(2):e0193465. doi: 10.1371/journal.pone.0193465. eCollection 2018.

    PMID: 29481572BACKGROUND
  • Roux-Sibilon A, Trouilloud A, Kauffmann L, Guyader N, Mermillod M, Peyrin C. Influence of peripheral vision on object categorization in central vision. J Vis. 2019 Dec 2;19(14):7. doi: 10.1167/19.14.7.

    PMID: 31826252BACKGROUND
  • Peyrin C, Roux-Sibilon A, Trouilloud A, Khazaz S, Joly M, Pichat C, Boucart M, Krainik A, Kauffmann L. Semantic and Physical Properties of Peripheral Vision Are Used for Scene Categorization in Central Vision. J Cogn Neurosci. 2021 Feb 11:1-15. doi: 10.1162/jocn_a_01689. Online ahead of print.

    PMID: 33571079BACKGROUND

MeSH Terms

Conditions

Glaucoma, Open-Angle

Condition Hierarchy (Ancestors)

GlaucomaOcular HypertensionEye Diseases

Central Study Contacts

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

August 23, 2022

First Posted

September 14, 2022

Study Start

October 1, 2022

Primary Completion (Estimated)

July 1, 2026

Study Completion (Estimated)

July 1, 2027

Last Updated

September 14, 2022

Record last verified: 2022-08

Data Sharing

IPD Sharing
Will share

Anonymized individual participant data will be share in the context of publications through the Open Science Framework, a tool that promotes open, centralized workflows.

Time Frame
Data will become available after publications with no limit time
Access Criteria
Link to the Open Science Framework