Using Shared Decision Making to Improve Kidney Transplantation Rates

Sponsor
Columbia University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06141499
Collaborator
Kidney Transplant Collaborative (Other), National Kidney Foundation (Other)
450
2
2
13.7
225
16.5

Study Details

Study Description

Brief Summary

The goal of this clinical trial is to increase shared decision-making between dialysis providers and patients in order to increase patients' probability of transplantation and to reduce socioeconomic/racial disparities in access to kidney transplantation.

Participants will receive educational material over the course of 6-12 months about different aspects of the kidney transplant and waitlisting process.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Provider educational materials
  • Behavioral: Patient letters
N/A

Detailed Description

Kidney transplantation is the preferred treatment choice for patients with end stage kidney disease (ESKD), yet only a small proportion of patients with incident ESKD are counseled about their transplant options. Often, a smaller minority of patients reach the transplant waitlist in a timely manner. Increasing the likelihood of transplantation for patients with ESKD can lead to longer survival, better quality of life, and reduced costs of care.

The kidney transplant and waitlist process is a complex and multi-step process that occurs over an extended period of time. This process involves transitions of care between multiple providers and requires patients to be proactive in their medical evaluations.

This study will deliver educational materials to dialysis care teams and provide quarterly, personalized informational letters to patients, with the aim of increasing shared decision-making between patients and providers by giving them the information needed to initiate conversations about kidney transplantation.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
450 participants
Allocation:
Non-Randomized
Intervention Model:
Single Group Assignment
Intervention Model Description:
Enrolled providers and enrolled patients will receive different interventions; outcomes assessed for these two groups will be different.Enrolled providers and enrolled patients will receive different interventions; outcomes assessed for these two groups will be different.
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Using Shared Decision Making to Improve Kidney Transplantation Rates
Anticipated Study Start Date :
Dec 1, 2023
Anticipated Primary Completion Date :
Oct 31, 2024
Anticipated Study Completion Date :
Jan 20, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Providers

Dialysis providers will receive educational material about the kidney transplantation and waitlisting process.

Behavioral: Provider educational materials
Dialysis providers will receive educational material about the kidney transplantation and waitlisting process.

Experimental: Patients

Dialysis patients will receive letters with information about their status within the kidney transplantation and waitlisting process.

Behavioral: Patient letters
Dialysis patients will receive letters with information about their status within the kidney transplantation and waitlisting process. Letters will describe kidney waitlist status, living donor transplantation, Hepatitis C positive kidney transplants, and high Kidney Donor Profile Index (KDPI) transplants.

Outcome Measures

Primary Outcome Measures

  1. Change in patient knowledge of individual waitlist status [Baseline (day 1), post letter 1 (6 weeks-3 months later), post letter 2 (6 weeks-3 months later), post letter 3 (6 weeks-3months later), post intervention (approximately 6-12 mos total)]

    Patient knowledge of individual waitlist status will be measured by one Yes/No question on the patient survey using McNemar's test.

  2. Change in frequency of shared decision-making conversations, [Baseline (day 1), post letter 1 (6 weeks-3 months later), post letter 2 (6 weeks-3 months later), post letter 3 ( 6weeks-3months later), post intervention (approximately 6-12 mos total)]

    Frequency of shared decision-making conversations will be measured by two Yes/No questions on the patient survey using McNemar's test.

  3. Change in donor kidney preferences [Baseline (day 1), post letter 1 (6 weeks-3 months later), post letter 2 (6 weeks-3 months later), post letter 3 (6 weeks-3months later), post intervention (approximately 6-12 mos total)]

    Patient preferences for kidneys from living donors, kidneys from Hepatitis C positive donors, and kidneys from high KDPI donors will be measured by six Yes/No questions on the patient survey using McNemar's test.

Secondary Outcome Measures

  1. Change in dialysis provider attitudes, as measured on provider survey [Post-educational session, Day 1]

    Dialysis providers' attitudes and comfort with discussing the kidney waitlist and transplantation process will be measured on the provider survey. Questions will be scored on a 1-5 Likert scale, with 1 indicating low comfort level and 5 indicating high comfort level. Total scores range from 5-25 with a higher score indicating a better outcome.

  2. Provider assessment of patient letters, as measured on provider survey [End of intervention/at completion of letter delivery (6-12 months)]

    Providers' assessment of the helpfulness of patient letters will be measured by five questions on the provider survey. Questions will be scored on a 1-5 Likert scale, with 1 indicating low helpfulness and 5 indicating high helpfulness. Total scores range from 5-25 with a higher score indicating a better outcome.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • On a waitlist or undergoing an evaluation at the Columbia University/New York Presbyterian Hospital (CU/NYPH) Transplant Center or at the Cleveland Clinic (CC)

  • Receiving hemodialysis at one of the following dialysis clinics:

  • Fresenius Kidney Care City Dialysis

  • DaVita Kidney Care Haven Dialysis

  • DaVita Melrose Dialysis

  • DaVita Highbridge Dialysis

  • Rogosin Institute East Side Dialysis Unit

  • Rogosin Institute West Side Dialysis Unit

Exclusion Criteria:
  • Speaking a language other than English or Spanish

  • Younger than 18 years of age

Contacts and Locations

Locations

Site City State Country Postal Code
1 Columbia University New York New York United States 10032
2 Cleveland Clinic Cleveland Ohio United States 44195

Sponsors and Collaborators

  • Columbia University
  • Kidney Transplant Collaborative
  • National Kidney Foundation

Investigators

  • Principal Investigator: Sumit Mohan, MD, MPH, Columbia University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Columbia University
ClinicalTrials.gov Identifier:
NCT06141499
Other Study ID Numbers:
  • AAAU1202
First Posted:
Nov 21, 2023
Last Update Posted:
Nov 30, 2023
Last Verified:
Nov 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Columbia University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 30, 2023