Peripherex Home Visual Field Demonstrates High Test-Retest Reliability, Validity
- PMID: 40547871
- PMCID: PMC12182241
- DOI: 10.2147/OPTH.S523260
Peripherex Home Visual Field Demonstrates High Test-Retest Reliability, Validity
Abstract
Purpose: Assessment of disease and progression is one of the greatest unmet needs in glaucoma care. Moving visual field testing into the home stands to increase access and increase testing frequency to address these unmet needs. Here, we test a novel home-based app (Peripherex Visual Field Test or PRX-VFT) that leverages eye tracking in a short, "gamified" software environment, against in-office Humphrey Field Analyzer (HFA) data.
Methods: Observational, multicenter, open-label clinical trial in patients diagnosed with glaucoma, glaucoma suspect, or ocular hypertension.
Results: A total of 190 PRX tests were performed with 97 on the left eye and 93 on the right eye, derived from 36 eyes of 19 patients who also had reliable, matched HFA data. Patients were 58% female with a mean (SD) age of 61.5 (11.9) years (range 26-78). Test-retest reliability was good, with interclass correlation coefficient of 0.7596. Detection of abnormal fields was excellent, with a sensitivity of 95.7% and a negative predictive value (NPV) of 98.27%. Detection of normal fields was very good, with a specificity of 79.26% and a positive predictive value (PPV) of 66.36%. Patients reported that compared to HFA, PRX-VFT was easier and more fun to complete.
Conclusion: In-home visual field testing using PRX-VFT on a patient's personal computer met its primary clinical trial endpoints, was feasible, and showed excellent statistical correlation to in-office HFA testing. PRX-VFT represents an opportunity for enhancing patient care at minimal additional equipment cost to the patient or healthcare system.
Keywords: glaucoma; home healthcare; prospective clinical trial; visual field test.
Plain language summary
The Peripherex Visual Field Test (PRX VFT) uses a patient’s home computer or laptop with built-in eye tracking and patented algorithms. For this study, the PRX VFT was tested in the real-world, in-home setting, compared to in-office Humphrey visual field tests. The PRX VFT used at home showed excellent statistics against in-office testing, meeting primary endpoints in an IRB-approved multicenter clinical trial for FDA registration. These data support in-home use of the PRX VFT by the eye care provider for screening and monitoring in glaucoma, and may be extended to the screening and monitoring of other retinal, optic nerve and neurological diseases.
© 2025 Schweitzer et al.
Conflict of interest statement
Dr Mitch Ibach reports personal fees from Zeiss and Glaukos, outside the submitted work. Dr John Berdahl reports personal fees from AbbVie, Aerpio, ALJ Health, Alcon, Aldeyra, Aquea Health, Aurion Biotech, Avelino, Balance Opthalmics, Bausch & Lomb, Belkin, CorneaGen, Dakota Lions Eye Bank, Elios Vision Inc, Expert Opinion, Glaukos, Gore, Greenman, Horizon Surgical, Iacta Pharmaceuticals, Imprimis, iRenix, IVERIC Bio, Inc, J&J, Kala, LayerBio, MELT Pharmaceuticals, MicroOptx, New World Medical, Ocular Surgical Data, Ocular Therapeutix, Omega Opthalmic, Orasis, Oyster Point, RXSight, Santen, Sight Sciences, Surface Inc, Tarsus, TavoBio, Tear Clear, Tissue Gen, True North CRO, Vance Thompson Vision, Verana Health, Versea Biologics, Vertex Ventures, and ViaLase, outside the submitted work. Mr Yitzi Kempinski reports personal fees from Peripherex, Inc, outside the submitted work; In addition, Mr Yitzi Kempinski has a patent EP4504031A1 pending to Peripherex Inc, patents US9746918B2, US10254831B2 and US9911037B2 issued to Umoove Services Ltd. Dr Jeffrey Goldberg reports a patent 16/087,327 licensed to Peripherex, a patent 63/327,388 pending to Peripherex, and shares in Peripherex. The authors report no other conflicts of interest in this work.
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