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Perceptual Learning Treatment for Amblyopia

Towards Developing a Perceptual Learning Treatment for Amblyopia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03788031
Enrollment
54
Registered
2018-12-27
Start date
2019-03-01
Completion date
2023-02-28
Last updated
2024-08-29

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

Conditions

Amblyopia

Brief summary

Objectives. To develop a new treatment for amblyopia using a perceptual learning approach. Hypothesis to be tested. Our proposed experiments are designed to investigate whether practicing a grating detection task can improve vision in patients with amblyopia. Design and subjects. A total of 36 patients with amblyopia will be randomized allocated into two intervention groups: Group 1, perceptual learning therapy. Group 2, occlusion therapy. A control group comprising of 18 subjects with normal vision will be recruited for comparison. A battery of tests will be used to assess a range of visual functions before and after the treatment intervention. Study instruments. Grating acuity testing system Interventions. We have established a clinical protocol for acuity training. On each trial, a properly oriented stimulus will be presented randomly at one of the four locations on a flat monitor screen. The visual task is to indicate the location of the stimulus. Participants will be required to undertake 20 one-hour sessions of training. Main outcome measures. Resolution acuity, visual acuity, contrast sensitivity function

Interventions

OTHERAcuity training

The intervention will be a vision therapy. On each trial, a properly oriented stimulus will be presented randomly at one of the four locations on a flat monitor screen. The visual task is to identify the location of the stimulus.

Participants will be required to patch the good eye for 20 days, 1 hour per day.

Sponsors

The Hong Kong Polytechnic University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
7 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Visual acuity in the amblyopic eye: 20/25 or worse

Exclusion criteria

* Manifest eye disease & nystagmus

Design outcomes

Primary

MeasureTime frameDescription
Change of grating acuity20 hoursGrating acuity tests the participants' ability to resolve fine details. This study measures the change of grating acuity after 20 hours of vision training.

Secondary

MeasureTime frameDescription
Change of visual acuity20 hoursVisual acuity tests the participants' ability to resolve letters.This study measures the change of visual acuity after 20 hours of vision training.
Change of contrast sensitivity20 hoursContrast sensitivity reflects the participants' sensitivity to identify low contrast visual stimuli. This study measures the change of contrast sensitivity after 20 hours of vision training.
Change of stereopsis20 hoursVisual acuity tests the 3-D perception. This study measures the change of stereopsis after 20 hours of vision training.

Countries

Hong Kong

Outcome results

None listed

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