Manhattan Vision Screening and Follow-Up Study

  • STATUS
    Recruiting
  • End date
    Sep 8, 2024
  • participants needed
    2373
  • sponsor
    Columbia University
Updated on 8 August 2021
eye exam
brimonidine tartrate ophthalmic solution

Summary

The investigators are conducting a 5-year prospective, cluster-randomized controlled trial, funded by the Centers for Disease Control (CDC), which provides vision screenings to underserved, vulnerable New York City residents living in affordable housing buildings in Harlem and Washington Heights.

Description

This study aims to increase engagement, detection and management of glaucoma, vision impairment, cataracts, and other eye diseases in vulnerable populations living in New York City. This study considers disparities by race, ethnicity, gender, geography, and socioeconomic status using innovative approaches such as patient navigators. Individuals over the age of 40 living in New York City Housing Authority (NYCHA) Housing buildings are eligible.

Details
Condition EYE DISORDER, Cataract, Ocular Hypertension, Glaucoma, Diabetic Retinopathy, Eye Disorders/Infections, Dry Eye Disease, Diabetic Macular Edema, Eye Disorders/Infections (Pediatric), Cataracts, Eye Disease, Vision Impairment and Blindness, ocular disease, ophthalmological disorder
Treatment Usual Care, Enhanced Intervention Using Patient Navigators
Clinical Study IdentifierNCT04271709
SponsorColumbia University
Last Modified on8 August 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Individuals over age 40
Living independently in NYCHA housing building
Willing to answer COVID-19 symptom questions
Willing to consent for 2 vision screening visits at baseline and 12-month follow-up

Exclusion Criteria

Self-reported terminal illness with life expectancy less than 1 year
Inability to provide informed consent due to dementia or other reasons
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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