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NCT05150197 · ClinicalTrials.gov registry record · NA

Virtual Reality Visual Field Testing as an Alternative in Childhood Eye Disease

A NA study of Visual Field Defect, Peripheral, sponsored by Duke University.

Recruiting
Registry status
NA
Development phase
1,000
Enrollment target
1
Study location

NCT05150197: Recruiting NA study of Visual Field Defect, Peripheral, sponsored by Duke University.

NCT05150197 is a NA study of Visual Field Defect, Peripheral that is actively recruiting participants, run by Duke University. The registered enrollment target is 1,000 participants, above the 32-participant average among 6 other Visual Field Defect, Peripheral trials with a reported enrollment target (3025% higher). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT05150197, a NA study of Visual Field Defect, Peripheral, is actively recruiting participants, sponsored by Duke University.

RECRUITING
Registry status
NA
Development phase
1,000 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to test a new way of measuring the peripheral vision (called a visual field test) using a device which can be worn as goggles rather than being a large instrument the patient must sit at. This new visual field test (called VisuALL) is an FDA-approved virtual reality system which has been used in adults and children. This study will compare the performance of the VisuALL to the standard testing for peripheral vision, which is called the Humphrey Visual Field (HVF) test. The study will recruit both healthy children, as well children and young adults who have eye conditions which require visual field testing as part of their standard care. The test will be performed on a day when the child or young adult already has a scheduled eye appointment as standard care. The test does not touch the eyes or require any eye drops to be given, and there is no known risk associated with the test itself. There may be a risk of loss of confidentiality. Participating in this study will require approximately 30 minutes, has no extra cost associated with it, and will be compensated by a parking pass for the day of the visit. There are no direct benefits for participants. Selected participants will be also be given training and then loaned a home VisuALL system to allow home visual field testing. If your child is selected, additional information would be provided.

Primary Outcome

Mean deviation of the visual field is one score measured in decibels calculated from device reading

Interventions

  • DEVICE VisuALL
  • DEVICE Humphrey Visual Field

Study Locations (1)

North Carolina

  • Duke University Medical Center - Durham

Trial Details

FieldValue
Enrollment Target 1,000 participants
Start Date 2022-01-19
Est. Completion 2026-02-01
Phase NA
Duke University

1,725 total trials

What NCT05150197 shows while recruiting

NCT05150197 is an interventional study that assigns participants to a tested intervention. Its 1,000 participants enrollment target places it among the larger protocols in the corpus, above the 32-participant average among 6 other Visual Field Defect, Peripheral trials with a reported enrollment target (3025% higher).

The record links to 1 condition, with Visual Field Defect, Peripheral appearing as the primary indexed condition, and to 2 interventions - of which VisuALL is the first listed.

NCT05150197 reports a single indexed study location in North Carolina.

Frequently Asked Questions

What is clinical trial NCT05150197 about?

NCT05150197 is a clinical study titled "Virtual Reality Visual Field Testing as an Alternative in Childhood Eye Disease". The purpose of this study is to test a new way of measuring the peripheral vision (called a visual field test) using a device which can be worn as goggles rather than being a large instrument the patient must sit at. This new visual field test (called VisuALL) is an FDA-approved virtual reality syst...

What is the current status of trial NCT05150197?

This trial is currently recruiting. It is a NA study. The enrollment target is 1,000 participants. The study started on 2022-01-19. Estimated completion is 2026-02-01.

What conditions does trial NCT05150197 study?

This clinical trial studies the following conditions: Visual Field Defect, Peripheral.

What interventions are being tested in trial NCT05150197?

The interventions under investigation include: VisuALL (DEVICE), Humphrey Visual Field (DEVICE).

Who is sponsoring clinical trial NCT05150197?

This trial is sponsored by Duke University, which has 1,725 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05150197 being conducted?

This trial has 1 study location across North Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT05150197, the US trial registry maintained by the National Library of Medicine. NCT05150197 (large enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.