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Exploring Perceptual Learning in Blurred Gabor Discrimination for Low-Myopic Children

Investigating the Efficacy of Perceptual Learning in Blurred Gabor Discrimination Among Children With Low Myopia: An Exploratory Study

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07107646
Enrollment
30
Registered
2025-08-06
Start date
2026-09-01
Completion date
2027-07-31
Last updated
2026-08-14

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

Conditions

Myopia, Perceptual Learning, Visual Rehabilitation

Keywords

Low Myopia, Perceptual Learning, Visual Acuity, Visual Evoked Potentials

Brief summary

This exploratory study investigates whether perceptual learning using blurred Gabor stimuli can improve uncorrected distance visual acuity in children aged 6-10 years with low myopia. Participants will be randomly assigned to a training group or control group. The training group will undergo individualized visual perceptual learning through a digital Vision Training System (VTS) for approximately 3 months. The study will also evaluate changes in refraction, contrast sensitivity, visual crowding, Chinese reading acuity with eye movements, and sweep visual evoked potentials (sVEPs).

Detailed description

Perceptual learning (PL) is a non-invasive approach that enhances visual function through repeated visual tasks. Prior studies have demonstrated its potential in treating amblyopia and age-related visual decline. However, its application in children with low myopia remains underexplored. This study has two main objectives: To examine the effect of perceptual learning using blurred Gabor stimuli on uncorrected distance visual acuity in children with low myopia. To investigate whether such training also improves refraction, contrast sensitivity, visual crowding, reading vision with eye movement patterns, and sweep visual evoked potentials (sVEPs). Thirty children aged 6-10 years with spherical equivalent refractive errors between -0.50 and -1.25 diopters (including ≤ -0.75 diopters of astigmatism) will be enrolled. Participants will be randomized into a training group or control group. The training group will undergo approximately 20 sessions of individualized visual perceptual learning using the Vision Training System (VTS), developed in collaboration with Bar Ilan University. Outcomes will be assessed before and after the intervention, and at follow-up points up to 12 months. Measures include visual acuity, refractive status, contrast sensitivity (CSV-1000E), crowding acuity (FrACT), Chinese reading visual acuity (with Tobii eye tracking), and sVEPs.

Interventions

BEHAVIORALvision training system, VTS

Participants in this group will receive individualized visual perceptual learning using the Vision Training System (VTS). The training involves blurred Gabor stimuli presented via a computer-based application. Each participant will complete approximately 20 training sessions over 3 months, with each session lasting 15 to 30 minutes, conducted twice per week. The program is designed to enhance uncorrected visual acuity, contrast sensitivity, and other visual functions by engaging neural mechanisms related to perceptual learning. Training progression is adaptive based on individual performance. The VTS software was developed in collaboration with Bar Ilan University.

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
6 Years to 10 Years
Healthy volunteers
No

Inclusion criteria

Experimental and Control Group Inclusion Criteria: 1. Children aged between 6 to 10 years. 2. Best corrected distance visual acuity of 6/6 or 0.00 logMAR. 3. Diagnosed with low myopia after a comprehensive ophthalmologic examination, with a spherical equivalent refractive error ranging from -0.50 to -1.25 diopters, including up to -0.75 diopters of astigmatism. 4. Not currently undergoing any of the four standard myopia control treatments for children: 1. Atropine (mydriatic agent) 2. Orthokeratology 3. Peripheral defocus soft contact lenses 4. Peripheral defocus spectacle lenses (frame glasses) 5. Willing and able to provide informed consent, and able to comply with study procedures and assessments.

Exclusion criteria

Participants will be excluded if they have any of the following ophthalmologic conditions: 1. Strabismus 2. Binocular vision problems 3. Ocular diseases 4. History of ocular surgery (excluding refractive surgery)

Design outcomes

Primary

MeasureTime frameDescription
Change in Best Corrected Visual Acuity (BCVA) From BaselineFrom enrollment to 12 months after completion of the 3-month training programBest Corrected Visual Acuity (BCVA) will be measured using the ETDRS or Snellen chart at a distance of 3 meters under standardized lighting conditions. The change in BCVA from baseline to post-training will be assessed.

Secondary

MeasureTime frameDescription
Change in Contrast Sensitivity Across Spatial Frequencies From BaselineFrom enrollment to 12 months after completion of the 3-month training programContrast sensitivity will be measured using the CSV-1000E test at a distance of 2.5 meters, assessing spatial frequencies at 3, 6, 12, and 18 cycles per degree (cpd). Changes from baseline will be evaluated.
Change in Visual Crowding Acuity From BaselineFrom enrollment to 12 months after completion of the 3-month training programVisual crowding acuity will be assessed using the Freiburg Vision Test (FrACT) before and after the training program. Changes from baseline will be evaluated.
Change in Reading Visual Acuity and Eye Movement Parameters From BaselineFrom enrollment to 12 months after completion of the 3-month training programReading visual acuity and eye movements will be assessed using a custom Chinese reading test for children. Eye movements will be recorded using a Tobii eye tracker. Measured metrics include critical print size, maximum reading speed, and maximum reading acuity. Changes from baseline will be evaluated.
Change in Visual Acuity Measured by Sweep Visual Evoked Potentials (sVEP) From BaselineFrom enrollment to 12 months after completion of the 3-month training programObjective visual acuity will be measured using the sweep visual evoked potentials (sVEP) technique. Neural responses will be compared between pre- and post-training assessments to evaluate changes in visual acuity.
Change in Spherical Equivalent Refraction (Diopters) From BaselineFrom enrollment to 12 months after completion of the 3-month training programSpherical equivalent refraction will be measured using both automated and subjective refraction methods. Changes in spherical equivalent diopters will be assessed and compared between groups.

Countries

Taiwan

Contacts

CONTACTLi-Ting Tsai, PhD
litingtsai@ntu.edu.tw886-2-33668164

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 15, 2026