Community Glaucoma Screening Follow-up
Not Applicable
Completed
- Conditions
- Glaucoma
- Registration Number
- NCT00956865
- Lead Sponsor
- Wills Eye
- Brief Summary
The purpose of this study is to determine if one of three interventions improves follow-up rates for screening exam participants who are instructed to have a definitive eye exam.
- Detailed Description
To determine if one of three interventions: vouchers, telephone calls, and personal contacts, improves follow-up rates for screening exam participants who are instructed to have a definitive eye exam.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
- All who had an eye screening exam.
Exclusion Criteria
- None
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Definitive follow-up eye exam 3 months
- Secondary Outcome Measures
Name Time Method