Skip to main content
OpenTrials
Completed

NCT Number: NCT04786886

Patient Performance and Acceptance of Virtual Reality Visual Field Devices

The purpose of this research is to study the effectiveness and patient experience when measuring visual fields using virtual reality goggles.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Visual Field Defect, Peripheral Visual Field Defect, Nasal Step Visual Field Defect, Paracentral Scotoma of Both Eyes

Age range

13 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Bascom Palmer Eye Institute

Miami, Florida, 33136, United States

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Any patient >13 years old at Bascom Palmer Eye Institute
  • Patients who either have glaucoma, are glaucoma suspects, or have a strong family history of glaucoma

Exclusion criteria

  • Adults unable to consent, pregnant women, prisoners
  • Patients under the age of 13

Treatment and study plan

VIrtual Reality Visual Field Exam

Other

Virtual reality visual field exam will be administered using the virtual reality headset. Exams can take up to 20 minutes.

Primary outcomes

  1. Operational Effectiveness

    Time frame: Day 1

    Operational effectiveness will be reported as the length of the visit and virtual reality visual field exam testing times. Both will be measured in minutes.

  2. Medical Effectiveness as Measured by Visual Field Indexes

    Time frame: Day 1

    Medical effectiveness will be evaluated by visual field indexes, such as mean deviation, pattern standard deviation, and foveal threshold, which are all measured in decibels. These values are generated based on the participants' performance in the visual field exam.

  3. Medical Effectiveness as Measured by Glaucoma Hemifield Test

    Time frame: Day 1

    Medical effectiveness will be evaluated by the glaucoma hemifield test. This value is generated based on the participants' performance in the visual field exam.

  4. Reliability Indices

    Time frame: Day 1

    Reliability index is generated based on the participants' performance in the visual field exam.

Sponsors and collaborators

Lead sponsor

University of Miami

Other

Registry information

Important dates

Study start
2019
Primary completion
2021
Study completion
2021
First posted
Mar 8, 2021
Registry last updated
Mar 8, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.