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Effectiveness of the Smartphone Application in Increasing Compliance to Occlusion Therapy in Children with Amblyopia: A Randomized Controlled Trial

Effectiveness of the Smartphone Application in Increasing Compliance to Occlusion Therapy in Children with Amblyopia: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20180523003
Enrollment
106
Registered
2018-05-23
Start date
2018-10-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Amblyopia Amblyopia, Occlusion therapy, Compliance, Application, Randomized controlled trial

Interventions

In ATCU group will be prescribed patching and use Amblyopia Treatment Chulalongkorn University (ATCU) application to record patching hours. Caregivers will observe and estimate how many hours that pat
Experimental Device,No Intervention Other
ATCU application group,Control group

Sponsors

Ratchadapiseksompotch Fund
Lead Sponsor

Eligibility

Sex/Gender
All
Age
4 Years to 12 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria 1. Children aged 4-12 years who have been diagnosed with unilateral strabismic, anisometropic, deprivation, or mixed type amblyopia in King Chulalongkorn Memorial Hospital and Rutnin Eye Hospital 2. Best-corrected visual acuity in the amblyopic eye between 20/40 and 20/400 3. At least 2 lines difference in visual acuity between both eyes 4. No previous treatment of amblyopia other than spectacles and occlusion therapy 5. Refractive error correction for a minimum of 4 weeks 6. Parents or caregivers have their own smart phone or tablet that is compatible with either iOS or android operating system 7. The same parents or caregivers, along with the child, are able to make a follow up visit at each appointment during the study

Exclusion criteria

Exclusion criteria: Exclusion criteria 1. Previous treatment for amblyopia other than spectacles and occlusion therapy 2. Presence of moderate to severe mental retardation or learning disability 3. Refractive error correction less than 4 weeks prior

Design outcomes

Primary

MeasureTime frame
Objective compliance of occlusion therapy First month and third month follow up A percentage of actual patching hours to prescribed patching hours

Secondary

MeasureTime frame
best corrected visual acuity 1 month and 3 months measured with the Snellen optotype and scored in logMAR unit

Countries

Thailand

Contacts

Public ContactWorawalun Honglertnapakul

Chulalongkorn university

Worawalunh@gmail.com66819153661

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026