Binocular Visual Therapy and Video Games for Amblyopia Treatment.

Sponsor
Universidad Autonoma de Nuevo Leon (Other)
Overall Status
Recruiting
CT.gov ID
NCT03655912
Collaborator
Hospital Universitario Dr. Jose E. Gonzalez (Other)
60
1
3
49.7
1.2

Study Details

Study Description

Brief Summary

Amblyopia, or lazy eye, is best defined by the American Academy of Ophthalmology as a unilateral or bilateral reduction of the best corrected visual acuity that occurs in the setting of an otherwise normal eye, or a structural abnormality involving the eye or visual pathway with reduction in visual acuity that cannot be attributed only to the effect of the structural abnormality. Which causes an abnormal visual experience early in life, with consequences such as deficiencies in the ability to perceive contrast and/or movement, visual acuity, accommodation and stereopsis. The treatment of choice consists in patching of the fellow eye 2 hours per day. The disadvantage of this treatment modality is that patients end up not complying and when treatment is interrupted, lazy eye reappears. Amblyopia was thought to be a monocular disease, now a days there are reports of cortical visual paths changes in both eyes (the fellow and amblyopia eye), believing that it might be a monocular consequence of a binocular disease. Following that statement new treatment studies have arisen, stimulating both eyes not only to improve visual acuity in the lazy eye, but to restore binocular function as well. These treatments use videogames in celular phones, computers, or tablets where the fellow eye is exposed to reduced contrast and the lazy eye is exposed to full-contrast. Although the evidence is promising, more studies are needed to establish effectivity and security of this treatment modality.

Condition or Disease Intervention/Treatment Phase
  • Device: Red/green glasses
  • Device: Electronic Tablet
  • Device: Eye patch
N/A

Detailed Description

The objective of this study is to determine if the binocular visual therapy with red-green glasses and the use of electronic devices is effective for amblyopia treatment in children.

Participants will be randomly assigned to one of three treatment modalities: Group A: eye patch on the fellow eye and to near-vision activities (such as reading, drawing, etc) Group B: an eye patch on the fellow eye and a electronic tablet Group C: red/green glasses and a electronic tablet

Treatment will be done buy the three groups daily during 2 consecutive hours, and will be completed for four months. Children will then suspend the therapy for 2 months, and will be reevaluated to determine lazy eye relapses . All groups will be compared to see which patients achieved greater improvement on visual acuity and depth perception.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Care Provider)
Masking Description:
Neither the patient or the care provider will be aware of the treatment modality group the patient is in. In order to achieve that, patients in different modality groups will be evaluated in different days preventing information of group modality gossip between the patients parents.
Primary Purpose:
Treatment
Official Title:
Binocular Visual Therapy and Video Games for Amblyopia Treatment.
Actual Study Start Date :
Oct 9, 2018
Anticipated Primary Completion Date :
Oct 1, 2022
Anticipated Study Completion Date :
Dec 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Patch

Eye patch on the fellow eye and to near-vision activities (such as reading, drawing, etc)

Device: Eye patch
The use of eye patch on the fellow eye and near vision activities for 2 hours a day during 4 months.

Experimental: Electronic Devices

Eye patch on the fellow eye and a electronic tablet

Device: Electronic Tablet
The use of eye patch on the fellow eye and electronic tablet for 2 hours a day during 4 months.

Experimental: Red/Green Glasses

Red/green glasses and a electronic tablet

Device: Red/green glasses
The use of red/green glasses and electronic devices for two hours a day during 4 months.

Outcome Measures

Primary Outcome Measures

  1. Best corrected visual acuity of the amblyopic eye [Basal]

    Best corrected visual acuity of the amblyopic eye using the Snellen chart. Measurements will be converted to LogMar values for statistical analysis.

  2. Best corrected visual acuity of the amblyopic eye [One month of treatment]

    Best corrected visual acuity of the amblyopic eye using the Snellen chart. Measurements will be converted to LogMar values for statistical analysis.

  3. Best corrected visual acuity of the amblyopic eye [Two months of treatment]

    Best corrected visual acuity of the amblyopic eye using the Snellen chart. Measurements will be converted to LogMar values for statistical analysis.

  4. Best corrected visual acuity of the amblyopic eye [Three months of treatment]

    Best corrected visual acuity of the amblyopic eye using the Snellen chart. Measurements will be converted to LogMar values for statistical analysis.

  5. Best corrected visual acuity of the amblyopic eye [Four months of treatment]

    Best corrected visual acuity of the amblyopic eye using the Snellen chart. Measurements will be converted to LogMar values for statistical analysis.

  6. Best corrected visual acuity of the amblyopic eye two months after treatment suspension to determine lazy eye relapses [Two months after treatment suspension.]

    Best corrected visual acuity of the amblyopic eye using the Snellen chart. Measurements will be converted to LogMar values for statistical analysis.

Secondary Outcome Measures

  1. Stereopsis [Basal]

    Stereopsis measurement by titmus test

  2. Stereopsis [One month of treatment]

    Stereopsis measurement by titmus test

  3. Stereopsis [Two months of treatment]

    Stereopsis measurement by titmus test

  4. Stereopsis [Three months of treatment]

    Stereopsis measurement by titmus test

  5. Stereopsis [Four months of treatment]

    Stereopsis measurement by titmus test

  6. Stereopsis two months after treatment suspension to determine lazy eye relapses [Two months after treatment suspension.]

    Stereopsis measurement by titmus test

Eligibility Criteria

Criteria

Ages Eligible for Study:
4 Years to 10 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with anisometropic amblyopia, strabismic amblyopia or both

  • Patients with out previous amblyopia treatment

  • Patient with previous strabismus surgery or use of there best corrected visual acuity glasses for at least 1 month

  • Birth at term gestational age

  • Without any systemic or ophthalmic comorbidities

  • Previous patients parent verbal and fiscal assessment.

Exclusion Criteria:
  • Any other amblyopia diagnosis (deprivation)

  • Any previous amblyopia treatment

  • Any previous intraocular surgery

  • Any ocular condition

  • Any neurologic conditions or psychomotor development alterations

  • Patients not able to cooperate for visual acuity or stereopsis evaluation

Contacts and Locations

Locations

Site City State Country Postal Code
1 Departamento de Oftalmologia, Hospital Universitario "Dr. Jose Eleuterio Gonzalez" Monterrey Nuevo Leon Mexico 64460

Sponsors and Collaborators

  • Universidad Autonoma de Nuevo Leon
  • Hospital Universitario Dr. Jose E. Gonzalez

Investigators

  • Principal Investigator: Marissa L. Fernandez-de Luna, MD, Universidad Autonoma de Nuevo Leon

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Karim Mohamed-Noriega, Professor, Universidad Autonoma de Nuevo Leon
ClinicalTrials.gov Identifier:
NCT03655912
Other Study ID Numbers:
  • OF17-00013
First Posted:
Aug 31, 2018
Last Update Posted:
May 18, 2022
Last Verified:
May 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Karim Mohamed-Noriega, Professor, Universidad Autonoma de Nuevo Leon
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 18, 2022