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Efficacy Evaluation of Fine Motor Training under Visual Guidance in the Treatment of Amblyopia

Efficacy Evaluation of Fine Motor Training under Visual Guidance in the Treatment of Amblyopia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600124821
Enrollment
Unknown
Registered
2026-05-18
Start date
2026-06-15
Completion date
Unknown
Last updated
2026-05-25

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

Conditions

Amblyopia

Interventions

Group 1 (Character Writing Training and Patching ? Patching Only):Character Writing Training + Patching
Group 3 (Character Matching Training and Patching ? Character Writing Training and Patching):Character Matching Training + Character Writing Training + Patching
Group 2 (Patching Only ? Character Writing Training and Patching):Patching + Character Writing Training

Sponsors

The First Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 14 Years

Inclusion criteria

Inclusion criteria: 1.Age 5 to 14 years, regardless of sex, and in good general health. 2.Diagnosed by an ophthalmologist with unilateral anisometropic amblyopia, unilateral strabismic amblyopia, or mixed amblyopia, with best-corrected visual acuity (BCVA) worse than 0.8 (decimal visual acuity) and an interocular BCVA difference of at least 2 lines. 3.Has worn corrective glasses based on the most recent refractive prescription for at least 2 weeks. 4.No ocular diseases other than amblyopia and possible concomitant strabismus (e.g., corneal disease, cataract, glaucoma, or retinal disease), and no systemic diseases affecting visual function. 5.No history of ocular trauma or ophthalmic surgery within the past year. 6.No history of neurological or psychiatric disorders that may interfere with study cooperation, such as intellectual disability, language impairment, or attention deficit. 7.The child and the legal guardian voluntarily agree to participate, sign the informed consent form, and are able to comply with the study protocol and complete follow-up assessments.

Exclusion criteria

Exclusion criteria: 1.Presence of obvious strabismus (>15 ?) that may affect visual axis stability and training efficacy. 2.Inability to continuously wear corrective glasses, or receipt of other visual training interventions during the study period (e.g., bead-threading training or visual perception software training). 3.Inability to complete the intervention as required, such as insufficient daily copybook training time or clearly inadequate training frequency. 4.Unwillingness to cooperate with follow-up assessments during the study period, or poor compliance. 5.Refusal by the child or legal guardian to sign the informed consent form, or withdrawal from the study during the study period.

Design outcomes

Primary

MeasureTime frame
Distance visual acuity;

Secondary

MeasureTime frame
Copying similarity score and matching accuracy;Minimum recognizable font size;Stereopsis;Near visual acuity;

Countries

China

Contacts

Public ContactFeng Lixia

The First Affiliated Hospital of Anhui Medical University

lixiafeng@163.com+86 551 62922324

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: May 30, 2026