An Exploratory Study on the Short-Term Additive Efficacy and User Experience of Innovative Gamified Intervention as an Adjunctive Therapy for Children with Monocular Anisometropic Amblyopia

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2500113962

Enrollment

Unknown

Registered

2025-12-04

Start date

2025-12-20

Completion date

Unknown

Last updated

2025-12-08

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

Conditions

amblyopia

Interventions

Group 1 (Intervention):Serious touchscreen game combined with occlusion

Group 2 (Intervention):Augmented Reality game combined with occlusion

Control Group:Occlusion therapy only

Eligibility

Sex/Gender

All

Age

4 Years to 7 Years

Inclusion criteria

Inclusion criteria: 1.Clinically diagnosed with monocular anisometropic amblyopia. 2.Aged 4 to 7 years. 3.Able to cooperate with all examinations and comply with the amblyopia training regimen. 4.Provided signed informed consent.

Exclusion criteria

Exclusion criteria: 1.Severe developmental delay or cognitive impairment. 2.Serious systemic diseases. 3.Presence of organic ocular diseases (e.g., cataract, fundus diseases) or manifest strabismus. 4.Participation in any other eye-related interventional trial within the past 4 weeks.

Design outcomes

Primary

Measure	Time frame
Objective improvement in visual function;	—

Secondary

Measure	Time frame
Improvement in functional vision in daily living;Emotional and psychological improvement;Compliance and acceptance;	—

Countries

China

Contacts

Public ContactJianing Ren

Xinhua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine

981433535@qq.com+86 188 0025 3186

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026