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Clinical Trials/NCT02389387
NCT02389387CompletedNot Applicable

Reducing Disparities in Access to Kidney Transplantation: The RaDIANT Regional Study

Emory University0 sites440 target enrollmentStarted: March 2015Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Enrollment
440
Primary Endpoint
Change in Referral Disparity from baseline

Study Overview

Brief Summary

The purpose of this study is to facilitate coordination of transplant centers in North Carolina, South Carolina, and Georgia to share kidney transplant referral data in patients with End-Stage Renal Disease (ESRD) who are candidates for kidney transplantation.

Detailed Description

Disparities exist in access to kidney transplantation where poor and minority patients are less likely to access each step of the kidney transplant process. Current national surveillance data does not capture information on transplant referral, and it is unclear to what extent dialysis facility-level factors may influence disparities in access to transplantation. Due to significant variability in the standardized transplant ratios observed at each facility, the investigators hypothesize that there may be facility-related reasons that impact disparities in access to the first step of the kidney transplant process -- referral to the transplant center to undergo an evaluation for the suitability for transplant.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Retrospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Kidney transplant centers in the geographic area of North Carolina (NC), South Carolina (SC) and Georgia (GA)
  • Low rates of referral for kidney transplantation (6-month crude referral risk mean of 0.06 and all facilities with a crude referral risk less than the mean)
  • The presence of a racial disparity (African American vs. Caucasian) in referrals for kidney transplantation (racial disparity calculated based on the crude referral risk difference and the standardized referral risk difference.)
  • The final pool of 440 facilities will be randomized to either the intervention or control group using a one to one ratio.

Exclusion Criteria

  • Close out date populated
  • Transplant and hospital-based facility
  • Home dialysis facility
  • Patient census <25
  • >100 miles from nearest transplant center
  • Non-profit facility (except Wake Forest University Dialysis)

Outcomes

Primary Outcomes

Change in Referral Disparity from baseline

Time Frame: Baseline, one year after completion of the intervention

Assessed by referral disparity ratio: percentage of African American patients over percentage of white patients referred (%AA referred/%white referred) to compare across intervention and control facilities at baseline and one year after completion of the intervention. This is a facility level outcome.

Secondary Outcomes

  • Change in number of referrals between Control and Experimental patients from baseline(Baseline, 6 months after referral, one year after referral)
  • Change in medical evaluation start racial disparity and waitlisting racial disparity(Baseline, 6 months after referral, one year after the start of medical evaluation)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Rachel Patzer

Assistant Professor

Emory University

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