Expired Study
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Detroit, Michigan 48202


Purpose:

Diabetic retinopathy is the major cause of blindness in working age Americans, and screening for it is cost-effective. There are a quarter of a million people in Southeast Michigan with diabetes and pre-diabetes. Only half of patients with diabetes are screened regularly for diabetic retinopathy, and this proportion has been difficult to increase despite various interventions. Previous research focused on HMO patient groups because preventative care was thought to decrease plan costs. In addition, it was administratively feasible to track patient-doctor interactions. This project builds on published research and institutional experience to determine an effective method for increasing the screening rate, in a mobile, non-HMO population. It uses administrative methods and information technology infrastructures, such as large scale electronic medical records and patient demographic databases, to identify existing patients requiring examinations. Patients were telephoned by a trained service representative who offered and scheduled firm examination appointment times. Hypothesis: Annual screening rates for diabetic retinopathy can be substantially improved in non-HMO patient groups by directly contacting patients and scheduling firm appointment times.


Criteria:

Inclusion Criteria: - were Henry Ford Health System patients, - diabetic - using the BCBSM payer plan Exclusion Criteria: - retina examination in prior year


Study is Available At:


Original ID:

F10030


NCT ID:

NCT00799695


Secondary ID:

F10030


Study Acronym:


Brief Title:

Diabetic Retina Exam Rate Does Not Increase With Phone Reminders in Non-HMO Population


Official Title:

Diabetic Retina Exam Rate Does Not Increase With Phone Reminders in Non-HMO Population


Overall Status:

Completed


Study Phase:

N/A


Genders:

Both


Minimum Age:

18 Years


Maximum Age:

N/A


Quick Facts

Healthy Volunteers
Oversight Has DMC
Study Is FDA Regulated
Study Is Section 801
Has Expanded Access

Study Source:

Henry Ford Health System


Oversight Authority:

United States: Institutional Review Board


Reasons Why Stopped:


Study Type:

Interventional


Study Design:

Allocation: Randomized, Endpoint Classification:


Number of Arms:

1


Number of Groups:

0


Total Enrollment:

561


Enrollment Type:

Actual


Overall Contact Information

Official Name:Robert M Levine,, MD
Principal Investigator
Henry Ford Health System

Study Dates

Start Date:January 2008
Completion Date:November 2008
Completion Type:Actual
Primary Completion Date:May 2008
Primary Completion Type:Actual
Verification Date:November 2008
Last Changed Date:November 28, 2008
First Received Date:November 26, 2008

Study Outcomes

Outcome Type:Primary Outcome
Measure:a change in the proportion of diabetic patients who acted as a result of the phone contact, and obtained a retina eye exam.
Time Frame:3 months
Safety Issues:False

Study Interventions

Intervention Type:Behavioral
Name:phone call contact
Description:A sample of subjects who had not completed their annual diabetic screening exams were contacted by phone and offered appointments for eye exams

Study Arms

There are no available Study Arms

Study Agencies

Agency Class:Other
Agency Type:Lead Sponsor
Agency Name:Henry Ford Health System
Agency Class:Other
Agency Type:Collaborator
Agency Name:Blue Cross Blue Shield of Michigan Foundation

Sample and Retention Information

There are no available Sample and Retention Information

Study References

There are no available Study References

Data Source: ClinicalTrials.gov

Date Processed: January 21, 2020

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