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Binocular Cartoon Treatment for Lazy Eye

N/A
Waitlist Available
Led By Ben Thompson, PhD
Research Sponsored by University of Waterloo
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be younger than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4 weeks
Awards & highlights

Study Summary

This trial is testing a new binocular treatment for amblyopia in young children to see if it's more effective than patching.

Eligible Conditions
  • Lazy Eye
  • Strabismus

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 weeks
This trial's timeline: 3 weeks for screening, Varies for treatment, and 4 weeks for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Secondary outcome measures
Interocular contrast balance
Interocular suppression
Motor function
+3 more

Trial Design

3Treatment groups
Experimental Treatment
Active Control
Group I: Binocular cartoon treatment in officeExperimental Treatment1 Intervention
Participants will view a dichoptic binocular cartoon (provided by BBC) on the Nintendo 3DS-XL in office. They will continue to watch the cartoon for 60 minutes, 4 times a week, for 2 weeks. After 2 weeks, they will be given the option to continue for an additional 2 weeks (total of 4 weeks). Watching the cartoon does not require any special glasses. They will discontinue patching during this time.
Group II: Binocular cartoon treatment at homeExperimental Treatment1 Intervention
Participants will view a dichoptic binocular cartoon (provided by BBC) on the Nintendo 3DS-XL at home. They will continue to watch the cartoon for 60 minutes, 4 times a week, for 2 weeks. After 2 weeks, they will be given the option to continue for an additional 2 weeks (total of 4 weeks). Watching the cartoon does not require any special glasses. They will discontinue patching during this time.
Group III: Control groupActive Control1 Intervention
Participants will patch for 2 hours every day at home. After 2 weeks, they will be given the option to crossover to the teratment group for an additional 2 weeks (total of 4 weeks). Patching is a common treatment for amblyopia, often considered the "golden standard." It is the most common comparison as a "control" group in amblyopia and vision therapy literature.

Find a Location

Who is running the clinical trial?

University of WaterlooLead Sponsor
124 Previous Clinical Trials
209,324 Total Patients Enrolled
McGill UniversityOTHER
395 Previous Clinical Trials
999,343 Total Patients Enrolled
Queensland University of TechnologyOTHER
25 Previous Clinical Trials
16,978 Total Patients Enrolled

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Who else is applying?

What state do they live in?
Texas
What site did they apply to?
Retina Foundation of the Southwest
What portion of applicants met pre-screening criteria?
Met criteria
How many prior treatments have patients received?
1

Why did patients apply to this trial?

Recent research and studies
clinicaltrials.govStudy
A Patch Free Treatment for Young Children With Amblyopia
Ben Thompson 2020. "A Patch Free Treatment for Young Children With Amblyopia". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT04086524.
~6 spots leftby May 2025
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