Checkerboard patterns may train young brains to see better
NCT ID NCT06701617
First seen Aug 14, 2026 · Last updated Aug 14, 2026
Summary
This trial tests whether a visual stimulation program using flickering black-and-white checkerboard patterns can improve visual function in children with low vision. The study includes children with mild to moderate low vision as well as those with severe or profound multiple disabilities and visual impairments. The intervention is delivered either in person or remotely via telehealth, and its effects are measured with visual function tests and caregiver questionnaires. The goal is to see if this approach can enhance visual development and daily visual performance.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- restorative visual rehabilitation using black-and-white checkerboard patterns and a visual stimulation program
- What this could lead to
- If effective, this could offer a practical way to improve visual function in children with low vision, including those with multiple disabilities, and expand access through telehealth.
- What could go wrong
- The trial is early and the outcomes are measured with specialized assessments, so benefits may be modest or vary widely among children. Remote delivery may not work as well as in-person for some.
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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About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Nov 2024
- Expected to finish
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Jun 2028
An estimate. End dates often move.
- 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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1 month to 18 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.
Passive visual stimulation group Inclusion Criteria: 1. Children aged less than or equal to 18 years old. 2. The causes of visual disorder in children are unlimited. 3. The acuity of the children's better eye was ≤ 0.2. 4. Children with multiple disabilities and visual disorders typically exhibit developmental levels ranging from moderate to severe or below. 5. The parents of these children exhibit a positive attitude and are willing to cooperate with visual learning programs. 6. Infants under 1 year old with low vision without other developmental issues , under or equal to moderate developmental issues. Exclusion Criteria: 1. Significant refractive errors that affect acuity but are unable to cooperate with wearing corrective glasses in two training sessions. 2. Requires patching for monocular vision rehabilitation but is unable to cooperate with patching in two training sessions. 3. The individual is unable to adapt to the training environment and cooperate with visual learning in two sessions due to unstable emotions or difficulty adapting to the environment. Perceptual learning group Inclusion Criteria (1)Children aged less than or equal to 12 years old. (2)No restrictions on the causes of visual impairment in children. (3)The acuity of the children's better eye was ≤ 0.5 (4)If children have additional developmental issues, their disability severity should primarily be mild or moderate. (5)The primary caregiver demonstrates a positive attitude and is willing to cooperate with the visual training program. (6)The child is capable of completing calibration with an eye-tracking device. Exclusion Criteria 1. Significant refractive errors that severely affect vision, where the child cannot adapt to wearing corrective glasses within two training sessions. 2. Requires occlusion therapy for monocular visual rehabilitation but cannot cooperate with occlusion within two training sessions. 3. Inability to adapt to the training environment or cooperate with visual training due to emotional instability or difficulty adjusting within two training sessions. 4. Unstable physiological conditions (e.g., epilepsy, sleep disturbances) that prevent consistent participation in visual training.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Department of Occupational Therapy, College of Medicine, National Taiwan University
RECRUITINGTaipei, Taiwan
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Other studies related to the condition(s) this trial covers.
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