πŸ›οΈ Verified NIH Record β€’ Updated 2024-08-08

Perimetric Testing With Virtual Reality (NCT06549010)

A Pilot Study on the Repeatability of a Novel Perimetric Test Administered Via a Virtual Reality Headset.

🟒 Recruiting Observational / Diagnostic πŸ“‹ Clinical Research Protocol Sponsor: Envision Health Technologies, Inc.

🩺 Plain-English Summary (8th-Grade Level)

Perimetry is an essential component in the diagnosis and monitoring of glaucoma. Since the advent of Standard Automated Perimetry (SAP), one of the clinical standards has been the Humphrey Field Analyzer (HFA, Carl Zeiss AG, Oberkochen, Germany). Visual field (VF) testing provided by the HFA is standard-of-care in glaucoma clinics and other ophthalmology and optometry practices. However, the HFA is a large device that does not allow for examination outside the clinic and can be uncomfortable for patients with limited mobility. This study aims to evaluate a novel head-mounted perimeter against the HFA as an alternative method of VF testing. This new perimeter uses a Virtual Reality (VR) headset and a gamified version of VF testing to assess the visual function of healthy eyes and patients. The results of this study will potentially serve as pilot data for the design of a larger study that involves the full assessment of the VR headset and its VF test, based on various testing strategies.

Who can join: Review the eligibility criteria below.

Location: Illinois College of Optometry / Illinois Eye Institute β€” Chicago, Illinois

Age range: 25 Years to 70 Years

πŸ§ͺ Interventions in This Study

  • Perimetric test (DIAGNOSTIC_TEST)

πŸ“‹ "Do I Qualify?" β€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria β†—

πŸ“ All Participating Trial Locations (1 Sites)

  • Illinois College of Optometry / Illinois Eye Institute β€” Chicago, Illinois

πŸ“ž Contact the Study Coordinator

Phone: (312) 949-7303

Email: mchaglas@ico.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

πŸ’° Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA Β§ 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Glaucoma clinical trials

πŸ’‘ How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Contact the study coordinator using the phone/email above.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
πŸ›οΈ View Official NIH Record β†—