Recruiting

Video Treatment

Sponsor:

Retina Foundation of the Southwest

Code:

NCT05439200

Conditions

Amblyopia

Eligibility Criteria

Sex: All

Age: 3 - 7

Healthy Volunteers: Not accepted

Interventions

Asynchronous 3D movies

Patching

Study Details

Brief summary:

The purpose of this study is to determine whether viewing asynchronous movies leads to better visual outcomes in young children with amblyopia than standard-of-care occlusion therapy with an adhesive patch and whether this is associated with better adherence to treatment.

Conditions

Amblyopia

Study ID

NCT05439200

Start date

Aug 23, 2023

Status verified date

Apr, 2026

Completion date

Jun 30, 2027

Anticipated

Primary completion date

Jan 31, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 3 - 7

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • aged 3-7 years
  • male and female
  • strabismic, anisometropic, or combined mechanism amblyopia (visual acuity 0.3-0.8 logMAR)
  • interocular visual acuity difference ≥0.3 logMAR
  • wearing glasses (if needed) for a minimum of 8 weeks with no change in visual acuity at 2 visits ≥4 weeks apart
  • child's ophthalmologist and family willing to forgo standard patching treatment during the study

Exclusion Criteria:

  • prematurity ≥8 wk
  • coexisting ocular or systemic disease
  • developmental delay
  • strabismus >5 pd
  • myopia > -3.00D

Study Design

Enrollment

44 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Asynchronous movies

Asynchronous 3D movies

active comparator: Standard-of-care patching with an adhesive patch

Standard-of-care patching with an adhesive patch

Interventions

Asynchronous 3D movies

3D movies streamed at home for viewing on a handheld lenticular 3D screen

Patching

Adhesive patch to cover the fellow eye

Primary outcome measure

  • Change in amblyopic eye visual acuity using a logMAR chart [ Time Frame: 6 weeks ]

Central Contacts and Locations

Locations

Retina Foundation

Recruiting

Dallas, Texas, United States, 75241

Contacts

Principal Investigator:

Eileen E Birch, PhD

More Information

Sponsor

Retina Foundation of the Southwest

Last update posted

Apr 7, 2026

Last verified

Apr, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Retina Foundation of the Southwest on 2026-04-07.