Understanding Visual Confusion Using Stereoscopic Displays

NCT04957745 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 13

Last updated 2023-07-10

Study results available
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Summary

In this research study we want to test how people understand a visual scene when the same image is presented to both the eyes, but portions of these images are altered in terms of contrast, depth or in some cases motion.

Conditions

  • Diplopia
  • Binocular Vision Suppression
  • Binocular; Fusion, With Defective Stereopsis
  • Monocular Diplopia

Interventions

BEHAVIORAL

Binocular visual confusion (unilateral opaque)

The peripheral target was a horizontally drifting grating measuring 10° by 10°, with a spatial frequency of 1 cycle per degree and a temporal frequency of 3 Hz, and located at 10° above the fixation. For the binocular visual confusion condition, the non-transparent (opaque) peripheral target will be displayed on only one eye (unilateral opaque display).

BEHAVIORAL

Unilateral monocular visual confusion (unilateral see-through)

The peripheral target was a horizontally drifting grating measuring 10° by 10°, with a spatial frequency of 1 cycle per degree and a temporal frequency of 3 Hz, and located at 10° above the fixation. For the unilateral monocular visual confusion condition, the half-transparent peripheral target will be displayed on only one eye (unilateral see-through display).

BEHAVIORAL

Bilateral monocular visual confusion (bilateral see-through)

The peripheral target was a horizontally drifting grating measuring 10° by 10°, with a spatial frequency of 1 cycle per degree and a temporal frequency of 3 Hz, and located at 10° above the fixation. For bilateral monocular visual confusion condition, the half-transparent peripheral target will be displayed on both eyes (bilateral see-through display).

Sponsors & Collaborators

  • National Eye Institute (NEI)

    collaborator NIH
  • Massachusetts Eye and Ear Infirmary

    lead OTHER

Principal Investigators

  • JaeHyun Jung · Schepens Eye Research Institute

Study Design

Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
14 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-11-09
Primary Completion
2022-07-27
Completion
2022-07-27

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04957745 on ClinicalTrials.gov