Adult amblyopia
Conditions
Interventions
The experimental group:Temporal asynchronous binocular visual stimulation, by allowing the non-dominant eye to perceive the visual image first, and the dominant eye to receive the visual image later,
The control group:Temporally symmetrical binocular visual stimulation by allowing both eyes to receive visual images at the same time
Sponsors
China Rehabilitation Research Center
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: (1) Age 18 and above, regardless of gender; (2) Diagnosed as amblyopia patient through outpatient examination; (3) The difference in refractive power between binocular hyperopia spherical lenses is greater than 1.50 DS, or the difference in refractive power between cylindrical lenses is greater than 1.00 DC; (4) 0.2 logMAR difference in binocular vision; (5) Having undergone optical correction glasses for corrected vision for at least two months; (6) No organic lesions were found in both eyes during clinical examination; (7) Has not received any training on simple occlusion or other amblyopia within the past month;
Exclusion criteria
Exclusion criteria: (1) Clinical examination reveals organic lesions; (2) Participants have received simple occlusion or other amblyopia training within the past month; (3) Participants have any acute or chronic diseases or hereditary visual system diseases; (4) Participants have a history of strabismus; (5) Known to be allergic to dilated pupil drugs such as atropine; (6) Individuals with a known history of eye surgery; (7) Other situations where researchers consider it inappropriate to participate in clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| vision;contrast sensitivity; | — |
Secondary
| Measure | Time frame |
|---|---|
| stereopsis; | — |
Countries
China
Contacts
Public ContactZHOU JIE
China Rehabilitation Research Center
Outcome results
None listed