Virtual Reality Visual Field (VR-VF): Both devices administer a standard visual field test. The Humphrey is the gold standard desk top model and the VR-VF is a virtual reality headset designed to deliver visual field testing
Study summary
The goal of this clinical trial is to evaluate the feasibility of using virtual reality based visual field testing to monitor glaucoma in a clinical setting. This will be done through comparison of a virtual reality (VR) based device to the current gold standard Ziess Humphrey Field Analyzer (HFA). The main questions the study aims to answer are:
* Can both devices produce similar results in terms of detecting visual field defects and progression?
* Does the stage (early, moderate, advanced) of glaucoma impact results between the two devices?
Participants will perform both a standard and a VR based visual field test at each visit, for a total of 5 visits.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* \>18 years of age
* diagnosis of primary open-angle glaucoma
* ability to perform visual field testing
* capacity to provide informed consent to research protocol
Exclusion Criteria:
* diagnosis of secondary glaucoma or non-glaucomatous optic neuropathy
* previous intraocular surgery (excluding cataract surgery and minimally invasive glaucoma surgery)
* significant media opacity
* pregnancy
* seizure disorder
* cardiac pacemaker/other implantable device
* severe vertigo/balance disorder
Primary outcome measure(s)
Visual field point-wise threshold values — Measured during each visual field test on visits 1 through 5 (throughout study completion, average 2 months) Both the VR visual field and HFA produce threshold light sensitivity values measured in decibels (db) at the same locations in space (e.g., 24-2 protocol with stimuli 6 degrees apart at locations up to 30 degrees from central fixation)
Global indices of visual field loss — Measured during each visual field test on visits 1 through 5 (throughout study completion, average 2 months) Mean deviation (MD) and pattern standard deviation (PSD) are measurements of global field loss produced by both devices.
Reliability Indices — Measured during each visual field test on visits 1 through 5 (throughout study completion, average 2 months) Fixation losses, false positives, false negatives are recorded during each visual field test and reflect the reliability of the given test.
Trial sites (1)
Facility
City
Region
Status
Eadie Technologies Inc
Halifax
Nova Scotia
Recruiting
More Nova Scotia Health Authority trials in Canada
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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