Recruiting

Feasibility, Accuracy, and Reproducibility of Virtual Reality Visual Field Testing in Patients With Glaucoma

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…

ClinicalTrials.gov IDNCT07063537
PhaseNA
Enrollment60
SponsorNova Scotia Health Authority
Age18 Years and older
SexALL
I'm interested View official listing

Conditions studied

Glaucoma Open-Angle

About this study

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.

Interventions

Primary outcomes

Eligibility information

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

Study locations

Before you participate: Varda Clinical is an independent discovery tool, not the study sponsor or a medical provider. Eligibility can only be determined by the official study team. Discuss potential risks and benefits with a qualified healthcare professional.

Source: ClinicalTrials.gov. Record last refreshed by Varda Clinical: 2026-10-19.