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Checkerboard patterns may train young brains to see better

NCT ID NCT06701617

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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

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

About 200 people

The number the study aims to enrol. It can still change while the study runs.

Started

Nov 2024

Expected to finish

Jun 2028

An estimate. End dates often move.

Lead sponsor

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

1 month to 18 years

Sex

Anyone

Healthy volunteers

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

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.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • Department of Occupational Therapy, College of Medicine, National Taiwan University

    RECRUITING

    Taipei, Taiwan

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