Eye exercises may help children with a wandering eye, a trial puts it to the test
NCT ID NCT04487249
First seen Sep 03, 2026 · Last updated Sep 04, 2026 · Updated 1 time
Summary
This pilot trial tests whether 20 weeks of vision therapy, including office sessions and home exercises, can improve eye alignment control in children aged 8 to 16 with intermittent exotropia, a condition where one eye sometimes drifts outward. Researchers compare vision therapy to simple observation to see if the therapy reduces the frequency of the eye drifting. The results will help decide whether to run a larger, longer study.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Vision therapy (orthoptics), a program of office-based and home exercises to improve eye coordination and control
- What this could lead to
- If vision therapy improves eye control, it could offer a non-surgical option for children with intermittent exotropia and support a larger long-term trial.
- What could go wrong
- This is a small pilot study, so results may not be conclusive. Vision therapy requires time and effort, and not all children may respond.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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47 people
The number who actually took part.
- Started
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Oct 2021
- Finished
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Apr 2026
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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8 to 16 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Major Inclusion Criteria- * Age 8 - 16 years * Intermittent exotropia meeting all of the following: * Distance exodeviation of 15∆ to 35∆ by prism alternating cover test (PACT) * IXT, exophoria, or orthophoria at near * Near exodeviation that does not exceed the distance exodeviation by more than 10∆ * Mean distance control score of 2 points or more with at least one measure being 3 points or higher * Mean near control score less than 5 points * Random dot stereopsis of 200" or better on Preschool Randot Stereotest * Willingness to accept randomization and no plan to relocate in the next 6 months Major Exclusion Criteria- * Treatment for IXT or amblyopia (other than refractive correction) within 3 months prior to enrollment * Office-based vision therapy for IXT within 6 months prior to enrollment * Prior office-based vision therapy for IXT of ≥10 sessions * Prior strabismus, intraocular, or refractive surgery (including BOTOX injection)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Ohio State University
Columbus, Ohio, 43210, United States
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Salus University
Philadelphia, Pennsylvania, 19141, United States
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Southern California College of Optometry at Marshall B. Ketchum University
Fullerton, California, 92831, United States
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Southern College of Optometry
Memphis, Tennessee, 38104, United States
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Stanford University
Stanford, California, 94305, United States
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University of Alabama in Birmingham
Birmingham, Alabama, 35294, United States
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Other studies related to the condition(s) this trial covers.
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