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Behavioural Intervention
Asynchronous 3D Movies for Lazy Eye
N/A
Recruiting
Research Sponsored by Retina Foundation of the Southwest
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Diagnosed with strabismic, anisometropic, or combined mechanism amblyopia (visual acuity 0.3-0.8 logMAR)
Child's ophthalmologist and family willing to forgo standard patching treatment during the study
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 2, 4, 6, 8, and 10 weeks
Awards & highlights
No Placebo-Only Group
Summary
This trial tests if watching special movies can improve vision in children with amblyopia better than using an eye patch. The movies help the weaker eye work harder, potentially leading to better vision. Watching these movies has been shown to significantly improve vision in children with amblyopia.
Who is the study for?
This trial is for boys and girls aged 3-8 with lazy eye, who have been wearing glasses for at least 8 weeks without vision improvement. They must not have been born more than 8 weeks early or have other eye/systemic diseases or significant developmental delays.
What is being tested?
The study compares two treatments for lazy eye in children: the traditional patching method versus watching asynchronous 3D movies designed to improve vision. The goal is to see if the movie method works better and if kids stick with it more easily.
What are the potential side effects?
While side effects are not detailed, potential issues might include discomfort from not using standard patching or visual strain from viewing asynchronous movies.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I have been diagnosed with a type of lazy eye.
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My child's eye doctor and we agree to not use patching treatment during the study.
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I am between 3 and 8 years old.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 2, 4, 6, 8, and 10 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~2, 4, 6, 8, and 10 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Secondary study objectives
Adherence to patching measured with a sensor and adherence to viewing videos measured with the streaming log data
Change in amblyopic eye visual acuity using a logMAR chart
Change in depth of suppression assessed with the contrast balance index
+6 moreAwards & Highlights
No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.
Trial Design
2Treatment groups
Experimental Treatment
Active Control
Group I: Asynchronous moviesExperimental Treatment1 Intervention
Asynchronous 3D movies
Group II: Standard-of-care patching with an adhesive patchActive Control1 Intervention
Standard-of-care patching with an adhesive patch
Research Highlights
Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Common treatments for Lazy Eye (amblyopia) include occlusion therapy (patching the stronger eye), atropine drops, and vision therapy exercises. These treatments work by forcing the brain to use the amblyopic eye, thereby strengthening its visual processing capabilities.
Viewing asynchronous movies is a novel approach that also aims to improve visual outcomes by engaging the amblyopic eye through visual stimulation. This method matters for Lazy Eye patients because it can potentially enhance adherence to treatment and provide a more engaging and less intrusive way to improve vision, especially in young children.
[Treatment of strabismus with focused prisms in 1984].Low vision rehabilitation for better quality of life in visually impaired adults.A Review of Cochrane Systematic Reviews of Interventions Relevant to Orthoptic Practice.
[Treatment of strabismus with focused prisms in 1984].Low vision rehabilitation for better quality of life in visually impaired adults.A Review of Cochrane Systematic Reviews of Interventions Relevant to Orthoptic Practice.
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Who is running the clinical trial?
Retina Foundation of the SouthwestLead Sponsor
14 Previous Clinical Trials
1,545 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- You have severe strabismus, where your eyes are misaligned by more than 5 prism diopters.You were born at least 8 weeks early.I have been diagnosed with a type of lazy eye.I have another eye or body-wide disease.My child's eye doctor and we agree to not use patching treatment during the study.You have a delay in your development.You have severe nearsightedness.The difference in vision between your two eyes is significant.You have worn glasses, if necessary, for at least 8 weeks and your vision has not changed during two visits that were at least 4 weeks apart.I am either male or female.I am between 3 and 8 years old.
Research Study Groups:
This trial has the following groups:- Group 1: Asynchronous movies
- Group 2: Standard-of-care patching with an adhesive patch
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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