Understanding Visual Confusion Using Stereoscopic Displays

Sponsor
Massachusetts Eye and Ear Infirmary (Other)
Overall Status
Recruiting
CT.gov ID
NCT04957745
Collaborator
National Eye Institute (NEI) (NIH)
30
1
1
31.7
0.9

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Other: Visual confusion
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Monocular Visual Confusion for Field Expansion
Actual Study Start Date :
Nov 9, 2021
Anticipated Primary Completion Date :
Jul 1, 2024
Anticipated Study Completion Date :
Jul 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Other: Visual confusion

The study participants will respond to various visual confusion stimuli presented on a stereoscopic display designed to simulate binocular/monocular visual confusions

Other: Visual confusion
We will show peripheral target images on a background motion in a stereoscopic display. For the binocular visual confusion condition, the target peripheral image will be displayed on only one eye. For unilateral and bilateral monocular visual confusion conditions, the half-transparent peripheral image will be displayed on only one eye and both eyes, respectively.

Outcome Measures

Primary Outcome Measures

  1. Perceptual Dominance rate [Through study completion, an average of 4 months]

    The time perceived target image under visual confusion condition divided by the total viewing time (seconds).

Eligibility Criteria

Criteria

Ages Eligible for Study:
14 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Better than 20/40 visual acuity in the worse eye

  • No restrictions of the peripheral visual field: (at least 60 degrees vertically and 40 degrees horizontally)

  • At least 14 years of age (no upper age limit)

  • Able to give voluntary, informed consent

  • Able to understand English

  • Binocular vision parameters within normal limits (Stereopsis ≤ 100 arc sec on any stereo test)

Exclusion criteria:
  • Patients with any physical or mental disabilities, including cognitive dysfunction, balance problems, or other deficits that could impair their ability to respond to the stimuli presented in this study will be excluded

  • Being unable to complete sessions lasting 2-3 hours

Contacts and Locations

Locations

Site City State Country Postal Code
1 Schepens Eye Research Institute Boston Massachusetts United States 02114

Sponsors and Collaborators

  • Massachusetts Eye and Ear Infirmary
  • National Eye Institute (NEI)

Investigators

  • Principal Investigator: JaeHyun Jung, Schepens Eye Research Institute

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jaehyun Jung, Assistant Scientist, Massachusetts Eye and Ear Infirmary
ClinicalTrials.gov Identifier:
NCT04957745
Other Study ID Numbers:
  • 2021P001757
  • R01EY031777
First Posted:
Jul 12, 2021
Last Update Posted:
Nov 17, 2021
Last Verified:
Nov 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Jaehyun Jung, Assistant Scientist, Massachusetts Eye and Ear Infirmary
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 17, 2021