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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00591110
Acronym
inCharge
Enrollment
177
Registered
2008-01-11
Start date
2008-06-30
Completion date
2009-12-31
Last updated
2012-06-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Eye Care, Eye Disease, Vision

Brief summary

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.

Interventions

BEHAVIORALEye care education

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

BEHAVIORALSocial-contact control

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

Sponsors

Pfizer
CollaboratorINDUSTRY
University of Alabama at Birmingham
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
60 Years to No maximum
Healthy volunteers
Yes

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.

Design outcomes

Primary

MeasureTime frame
Change in the percentage of persons receiving comprehensive eye care from pre- to post- intervention6 months

Secondary

MeasureTime frame
Improvement in knowledge, attitudes, and values about vision, eye conditions, and eye care and reduction in perceived barriers to care.18 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 24, 2026