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Study of New Digital Games and Eye Patch Therapy for Children Aged 4 to 7 With Monocular Anisometropic Amblyopia Evaluating Vision Improvement and User Experience
Led by Xinhua Hospital, Shanghai Jiao Tong University School of Medicine · Updated on 2026-07-30
66
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to improve visual function in children aged 4 to 7 years who have monocular anisometropic amblyopia. It evaluates the short-term additive effects and user experiences of innovative gamified interventions combined with occlusion therapy compared to occlusion therapy alone. The study focuses on enhancing treatment effectiveness, motivation, emotion regulation, and overall clinical experience while reducing medical anxiety in children. Participants are randomly assigned to one of three groups a serious touchscreen game combined with occlusion therapy, an augmented reality game combined with occlusion therapy, or occlusion therapy alone. The games are specially designed for amblyopia training and are used together with daily occlusion therapy, which involves wearing an eye patch on the healthy eye for 4 hours each day. During the 3-month study period, children will be assessed for improvements in visual function, including best-corrected visual acuity using a LogMAR chart. Researchers will also measure functional vision in daily life, medical fear, anxiety levels, training compliance, and acceptance. The study involves parent-child interaction in home or various settings and aims to develop a personalized, engaging visual training system for everyday use.
CONDITIONS
Brief Title
A Study on the Efficacy and User Experience of Gamified Intervention for Children With Anisometropic Amblyopia
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Clinically diagnosed with monocular anisometropic amblyopia
- Aged 4 to 7 years
- Able to cooperate with all examinations and comply with the amblyopia training regimen
- Provided signed informed consent
You will not qualify if you...
- Severe developmental delay or cognitive impairment
- Serious systemic diseases
- Presence of organic ocular diseases such as cataract, fundus diseases, or manifest strabismus
- Participation in any other eye-related interventional trial within the past 4 weeks
Research Team
J
Jianing Ren
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