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OpenTrials
Completed

NCT Number: NCT00591110

Project inCharge: Increasing the Rate of Comprehensive Eye Care Utilization by Older African Americans Through Community-Based Eye Health Education Program

The study design is a randomized intervention evaluation. Ten senior centers in predominately African American communities in the Birmingham, Alabama will be selected as sites for the educational intervention. Five centers will be randomly assigned to receive an educational intervention communicating practical information about vision, eye conditions and eye care as pertinent to the older African American population. The other five centers will serve as social-contact controls, where participants will receive an engaging information session on a non-health related topic. The primary outcome of interest is the change in percentage of persons receiving comprehensive eye care from pre- to post- intervention. The secondary outcomes are the process outcomes of improvement in knowledge, attitudes, and values about vision, eye conditions, and eye care.

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Key information

Age range

60 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Alabama at Birmingham

Birmingham, Alabama, 35294, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • African Americans ages >=60 years residing in the communities targeted for intervention or control activities

Exclusion criteria

  • Persons who do not speak English, persons who are not community-dwelling.

Treatment and study plan

Eye care education

Behavioral

Participants will receive an educational intervention communicating practical information about vision, eye conditions and eye care pertinent to the older African American population

Social-contact control

Behavioral

Participants receive an engaging informational session on a non-health related topic

Primary outcomes

  1. Change in the percentage of persons receiving comprehensive eye care from pre- to post- intervention

    Time frame: 6 months

Secondary outcomes

  1. Improvement in knowledge, attitudes, and values about vision, eye conditions, and eye care and reduction in perceived barriers to care.

    Time frame: 18 months

Sponsors and collaborators

Lead sponsor

University of Alabama at Birmingham

Other

Collaborators

  • Pfizer

Registry information

Acronym: inCharge

Important dates

Study start
2008
Primary completion
2009
Study completion
2009
First posted
Jan 11, 2008
Registry last updated
Jun 28, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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