Implementation pRogram to Improve Screening and Management for CKD in Diabetes (Program 1) (IRIS-CKD)
Start Date
10/28/2025
Completion Date
4/1/2027
Summary
IRIS-CKD is an implementation study to improve guideline-recommended screening of chronic kidney disease (CKD) in individuals with type 2 diabetes (T2D) in the United States.
Detailed Description
IRIS-CKD Screening Program: will focus on CKD screening in T2D. We will identify patients with T2D that have not received appropriate screening for CKD within the last 15 months and randomize patients to receive either a home kit to complete CKD screening ("home kit") versus a standard laboratory order ("laboratory order"). The primary objective is to evaluate whether delivery of home testing kits versus standard laboratory testing influences the degree to which patients receive guideline-recommended CKD screening. Patients will complete approximately 3 months of follow-up.
Eligibility Criteria
Age Range: 18 years to No maximum
Interventions
(IRIS-CKD Screening Program): Home Kit
(IRIS-CKD Screening Program): Standard Lab Order
Conditions
Locations
University of Alabama
Birmingham, Alabama 35233
United States
Orlando Health
St. Petersburg, Florida 33701
United States
University of Michigan
Ann Arbor, Michigan 48109
United States
Essentia Health
Duluth, Minnesota 55805
United States
Duke University
Durham, North Carolina 27707
United States
Houston Methodist
Houston, North Carolina 77030
United States
Baylor Scott & White
Temple, Texas 76508
United States