Form deprivation amblyopia
Conditions
Interventions
VPL Group:visual perceptual learning treatment software
Traditional treatment group:fine visual training (bead threading training)
Sponsors
Eye & ENT hospital of Fudan University
Eligibility
Sex/Gender
All
Age
3 Years to 18 Years
Inclusion criteria
Inclusion criteria: 1.Age = 3 years and < 18 years, any gender; 2.Meet the diagnosis of unilateral form deprivation amblyopia: interocular visual acuity difference = 0.2 (= 0.2 logMAR). Amblyopic eye: = 1.70 logMAR. Fellow eye: for children aged 3 years, = 0.40 logMAR; for children aged 4 years, = 0.30 logMAR; for children aged 5 years and above, = 0.20 logMAR; 3.At least 1 month after unilateral congenital cataract surgery, with a posterior chamber intraocular lens implanted, condition stable, and no risk of infection; 4.Have undergone appropriate optical correction with spectacles for at least 16 weeks, or have stable distance visual acuity (defined as a change of < 0.1 logMAR between two consecutive examinations using the same test method at an interval of at least 8 weeks); the operated eye after congenital cataract surgery requires appropriate bifocal spectacles; 5.Strabismus may be present, but central fixation must be achievable; 6.No amblyopia treatment other than spectacle correction within 8 weeks prior to enrollment, and total duration of standardized amblyopia treatment = 1 year;any treatment received more than 8 weeks prior to enrollment is acceptable; 7.Signed informed consent, voluntary participation in this trial, and good compliance.
Exclusion criteria
Exclusion criteria: 1.Patients wearing contact lenses; 2.Inability to cooperate with treatment due to skin allergy, photosensitivity, etc. 3.Subjects with limited activity due to illness, medication, or emotional state; 4.Presence of other ocular diseases or conditions that cause decreased vision (including nystagmus, vitreoretinal diseases, optic nerve diseases, glaucoma, corneal diseases, etc.); 5.Severe developmental delay, craniocerebral diseases, or psychological disorders (that may interfere with treatment or assessment); 6.Currently participating in other studies that may directly or indirectly affect the results of this study; 7.Inability to complete the testing and training, or other conditions deemed by the investigator to make the subject unsuitable for participation in the trial.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| contrast sensitivity;best-corrected visual acuity; | — |
Countries
China
Contacts
Public ContactWu Lianqun
Eye & ENT hospital of Fudan University
Outcome results
None listed