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Efficacy and safety of iAVT in patients with amblyopia

Efficacy and safety of iAVT in patients with amblyopia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300074572
Enrollment
Unknown
Registered
2023-08-09
Start date
2023-08-15
Completion date
Unknown
Last updated
2023-08-21

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

Conditions

Amblyopia

Interventions

Experimental group:Perception learning training, once a day, according to the system set training 30 minutes, home training for 2 cycles (20 days), after 10 days of training. A total of six cycles of
Control group:Cover 2 hours/day for 90 days

Sponsors

ZhongShan Ophthalmic Center, Sun Yat-Sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
4 Years to 7 Years

Inclusion criteria

Inclusion criteria: 1) Patients with clinically confirmed amblyopia: anisometropia, strabismus or a combination of the two; 2) Amblyopia: 0.05-0.63 (inclusive); 0.05 is the upper limit of the visual acuity standard for low vision in China. In order to avoid including low vision people in the experiment, the amblyopia of the included subjects should be greater than 0.05. According to the rules of amblyopia, the lower limit of the normal value of visual acuity for children aged 3-5 years is 0.5, and the lower limit of the normal value of visual acuity for children aged 6 and above is 0.7. 3) Age 4-7 years old; 4) Written informed consent by the parent and/or legal guardian; 5) Patients with amblyopia who have not received any treatment other than contact lens wearing within the previous 6 months and have been wearing contact lenses for 3 months or more.

Exclusion criteria

Exclusion criteria: 1) Patients with other organic eye diseases that have not been treated; 2) history of neurological or psychiatric disorders; 3) failure to cooperate with the completion of visual function tests and iAVT visual training related to the experiment; 4) those who have received amblyopia treatments such as masking and amblyopia training apparatus in addition to wearing glasses within the past 6 months.

Design outcomes

Primary

MeasureTime frame
Amblyopia is the best corrected vision;

Secondary

MeasureTime frame
Contrast sensitivity;Near stereo vision function;Visual function quality of life assessment of children;Movement Assessment Battery for Children - Second Edition(MABC-2);

Countries

China

Contacts

Public ContactXinping Yu

ZhongShan Ophthalmic Center, Sun Yat-Sen University

yu-xinping@163.com+86 136 9585 4678

Outcome results

None listed

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