Brain Visual Perception Training for Prevention and Control of Premyopia

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age6-10
SponsorShanghai Eye Disease Prevention and Treatment Center

About this trial

The goal of this clinical trial is to investigate whether brain visual perception training can effectively prevent myopia in children with pre myopia. It will also learn about the safety of brain visual perception training.

The main questions it aims to answer are: Does brain visual perception training slow down the growth of axial length? What medical issues may participants encounter when using the brain visual perception training system? Researchers will compare participants who receive brain visual perception training with a control group to see if the training group can delay the onset of pre myopia in children Participants will: The training group will receive 20 minutes of brain visual perception training once a day for a period of one year. Follow up check ups at the hospital every 3 months. Keep a diary of the values of axial length and refractive diopter.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

None

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • brain visual perception training group

    Device

    Conduct brain visual perception training through a visual training system to improve binocular visual balance. Train 2 projects per day, each lasting 10 minutes.

Treatment groups

156 Participants
are divided into 2 treatment groups
Group A: brain visual perception training groupExperimental treatment 1 intervention
Group B: control groupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

changes in axial length after 1 year

the difference in the changes of axial length between the intervention group and the control group

Time frame
1 year after the baseline

Secondary outcomes

1

changes in cycloplegic spherical equivalent after 1year

the difference in the changes of cyclopegic spherical equivalent between the intervention group and the control group

Time frame
1 year after the baseline

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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