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Brain Visual Perception Training for Prevention and Control of Premyopia

Clinical Study on Brain Visual Perception Training for Prevention and Control of Myopia in Children with Premyopia

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06585657
Enrollment
156
Registered
2024-09-05
Start date
2024-09-15
Completion date
2026-03-31
Last updated
2024-09-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myopia Progressing, Visual Function

Keywords

brain visual perception training, premyopia

Brief summary

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.

Interventions

DEVICEbrain visual perception training group

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

Sponsors

Shanghai Eye Disease Prevention and Treatment Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
6 Years to 10 Years
Healthy volunteers
Yes

Inclusion criteria

Children aged 6-10 years with premyopia, defined as a cycloplegic spherical equivalent refraction (SER) of the more myopic eye in the range of -0.50 to 0.75 (inclusive) diopters (D) and having at least 1parent with an SER in either eye of -3.00D or less.

Exclusion criteria

Children have astigmatism of 1.50D or more, anisometropia of 1.50 D or more, strabismus and other ocular abnormalities, any systemic diseases, or a history of any myopia interventions.

Design outcomes

Primary

MeasureTime frameDescription
changes in axial length after 1 year1 year after the baselinethe difference in the changes of axial length between the intervention group and the control group

Secondary

MeasureTime frameDescription
changes in cycloplegic spherical equivalent after 1year1 year after the baselinethe difference in the changes of cyclopegic spherical equivalent between the intervention group and the control group

Contacts

Primary ContactWei Xu, PhD
vvxuwei@163.com+8618521513008
Backup ContactHaidong Zou, PhD
zouhaidong@sjtu.edu.cn+8613311986528

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026