An Active Approach to Treat Amblyopia: Perceptual Learning and Video Games

Sponsor
University of California, Berkeley (Other)
Overall Status
Recruiting
CT.gov ID
NCT01115283
Collaborator
National Eye Institute (NEI) (NIH)
50
1
3
118
0.4

Study Details

Study Description

Brief Summary

Amblyopia, a developmental abnormality that impairs spatial vision, is a major cause of vision loss, resulting in reduced visual acuity and reduced sensitivity to contrast. This study uses psychophysical measures to study neural plasticity in both adults and children with amblyopia.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Perceptual learning
  • Behavioral: Video Games
  • Behavioral: Occlusion therapy
N/A

Detailed Description

Amblyopia, a developmental abnormality that impairs spatial vision, is a major cause of vision loss, resulting in reduced visual acuity and reduced sensitivity to contrast. Our previous findings (see CITATIONS) show that the adult amblyopic brain is still plastic and malleable, suggesting that active approach is potential useful in treating amblyopia. The goal of this project is to assess the limits and mechanisms of neural plasticity in both normal and amblyopic spatial vision. This study uses psychophysical measures to study neural plasticity in both adults and children with amblyopia. Research participants will be asked to practice a visual discrimination task (perceptual learning) or to play video games with the amblyopic eye for a period of time. A range of visual functions will be monitored during the course of treatment.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Improving Spatial and Temporal Vision in Adult and Juvenile Amblyopia
Study Start Date :
Jul 1, 2015
Anticipated Primary Completion Date :
May 1, 2025
Anticipated Study Completion Date :
May 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Perceptual learning

Patients will be asked to practice a range of visual discrimination tasks for a period of time (each therapy session:1-2 hrs, 4-5 sessions/wk for ~1-6 months).

Behavioral: Perceptual learning
Research participants will be asked to practice a visual discrimination task (e.g. position acuity, contrast sensitivity, stereoacuity etc) in our laboratory for a period of time (2 hrs/day, 5 days/week).
Other Names:
  • vision therapy
  • vision training
  • Experimental: Occlusion therapy

    The fellow sound will be covered with a standard eye patch for a period of time (1-2 hrs/day, 4-5 days/wk for ~1-3 months). The idea is to push the brain to use the weaker amblyopic eye.

    Behavioral: Occlusion therapy
    Research participants will be required to cover the good eye during the day in order to push the brain to use the amblyopic eye (2 hrs/day, 5 days/week for 2-4 weeks).
    Other Names:
  • vision training,
  • vision therapy
  • Experimental: Video game

    Patients will be asked to play videogames for a period of time (each therapy session:1-2 hrs, 4-5 sessions/wk for ~1-6 months).

    Behavioral: Video Games
    Research participants will be asked to play "off-the-shelf" video games in our laboratory for a period of time (2 hrs/day, 5 days/week).
    Other Names:
  • vision therapy
  • vision training
  • Outcome Measures

    Primary Outcome Measures

    1. Amblyopic vision [9 months]

      Improvement in amblyopic vision : visual acuity and stereoacuity

    Secondary Outcome Measures

    1. Spatial vision [9 months]

      Improvement in spatial vision (eg. contrast sensitivity, positional acuity and spatial attention)

    2. Temporal vision [9 months]

      Improvement in temporal processing and temporal vision

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    5 Years to 75 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • adults and children (>5 years old) with normal vision or amblyopia

    • amblyopia: interocular VA difference of at least 0.1 logMAR

    Exclusion Criteria:
    • any ocular pathological conditions, nystagmus

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Minor Hall 486, School of Optometry, University of California, Berkeley Berkeley California United States 94720

    Sponsors and Collaborators

    • University of California, Berkeley
    • National Eye Institute (NEI)

    Investigators

    • Principal Investigator: Roger W Li, OD, PhD, School of Optometry, Univeristy of california-Berkeley
    • Principal Investigator: Dennis M Levi, OD, PhD, School of Optometry, Univerisity of California-Berkeley

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    University of California, Berkeley
    ClinicalTrials.gov Identifier:
    NCT01115283
    Other Study ID Numbers:
    • R01EY001728
    • R01EY001728
    First Posted:
    May 4, 2010
    Last Update Posted:
    Nov 24, 2021
    Last Verified:
    Nov 1, 2021
    Keywords provided by University of California, Berkeley
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Nov 24, 2021