Community Glaucoma Screening Follow-up
Primary Purpose
Glaucoma
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Voucher
Telephone Call
Contact
Sponsored by
About this trial
This is an interventional screening trial for Glaucoma focused on measuring Glaucoma, Intervention, Follow up
Eligibility Criteria
Inclusion Criteria:
- All who had an eye screening exam.
Exclusion Criteria:
- None
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Active Comparator
Arm Label
Voucher
Voucher and call
Voucher and call and contact
Arm Description
Voucher for transportation reimbursement
Voucher for transportation and telephone calls
Voucher for transportation, telephone calls, and a contact at the senior center
Outcomes
Primary Outcome Measures
Definitive follow-up eye exam
Secondary Outcome Measures
Full Information
NCT ID
NCT00956865
First Posted
August 10, 2009
Last Updated
November 26, 2016
Sponsor
Wills Eye
Collaborators
Temple University
1. Study Identification
Unique Protocol Identification Number
NCT00956865
Brief Title
Community Glaucoma Screening Follow-up
Official Title
Community Glaucoma Screenings: Assessment of Interventions to Improve Follow-up
Study Type
Interventional
2. Study Status
Record Verification Date
November 2016
Overall Recruitment Status
Completed
Study Start Date
September 2002 (undefined)
Primary Completion Date
September 2002 (Actual)
Study Completion Date
September 2002 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Wills Eye
Collaborators
Temple University
4. Oversight
Data Monitoring Committee
No
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Glaucoma
Keywords
Glaucoma, Intervention, Follow up
7. Study Design
Primary Purpose
Screening
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
100 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Voucher
Arm Type
Active Comparator
Arm Description
Voucher for transportation reimbursement
Arm Title
Voucher and call
Arm Type
Active Comparator
Arm Description
Voucher for transportation and telephone calls
Arm Title
Voucher and call and contact
Arm Type
Active Comparator
Arm Description
Voucher for transportation, telephone calls, and a contact at the senior center
Intervention Type
Other
Intervention Name(s)
Voucher
Intervention Description
Vouchers given to reimburse transportation
Intervention Type
Other
Intervention Name(s)
Telephone Call
Intervention Description
Telephone reminder calls
Intervention Type
Other
Intervention Name(s)
Contact
Intervention Description
Contact at senior center to encourage follow up
Primary Outcome Measure Information:
Title
Definitive follow-up eye exam
Time Frame
3 months
10. Eligibility
Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
All who had an eye screening exam.
Exclusion Criteria:
None
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeffrey D Henderer, MD
Organizational Affiliation
Temple University
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
Community Glaucoma Screening Follow-up
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