Network Interventions to Reduce Disparities in Living Kidney Donation

Sponsor
Penn State University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05255757
Collaborator
University of Pennsylvania (Other), University of Alabama at Birmingham (Other)
300
2
4
29.6
150
5.1

Study Details

Study Description

Brief Summary

For this current phase of the larger project, the investigators will survey transplant candidates as well as the participants family and friends to understand the barriers to volunteering and evaluation. This project will examine how network characteristics are associated with eventual living donor kidney transplant outcomes and test the efficacy of evidence-based interventions designed to assist kidney transplant candidates in participant donor search on a multi-center scale.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Script Intervention
  • Behavioral: Search Intervention
N/A

Detailed Description

The overall goal is to understand the process and assist participants who do not receive unsolicited offers to be evaluated as a living kidney donor in initiating and effectively conducting these critical conversations with participants kin and friends. In the search intervention, based on what they can tell investigators about the number, type, perceived health, perceived relationship, and potential willingness to donate, as well as analyses of data from the National Health and Nutrition Examination Survey (NHANES) investigators will counsel them on which members of participants family and friendship networks appear most biomedically promising as donors among the subset of these individuals that participants have not ruled out for known medical or perceived relationship reasons. In the rhetorical intervention, investigators will test non-coercive, promising verbal scripts that have proven promising in preliminary tests in vignette experiments in online and phone surveys.

AIM 1: Survey transplant candidates about their social network and transplant-related attitudes, knowledge, and characteristics; and randomize participants into one of two interventions or a control group.

AIM 2: Send network member participants a survey that measures potential donor attributes that are hypothesized to influence donation decisions, such as medical contraindications, blood type, health insurance status, and barriers to living donation.

AIM 3: Test whether participant social networks and interventions affect donation outcomes using medical records and follow-ups provided by Penn and UAB. Investigators will create the first predictive model of potential donor evaluation and actual donation. This information is critical to improve clinical practice and efforts to ethically influence the living donor search process.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
300 participants
Allocation:
Randomized
Intervention Model:
Factorial Assignment
Intervention Model Description:
There are two interventions randomly assigned to participants in a factorial experimental design. The first intervention is the search intervention. In addition to the candidate survey, transplant candidates assigned to this intervention will be given information about the statistical likelihood that each member of their social network will be free of contraindications for living kidney donation. The second intervention is the script intervention, where in addition to the survey, transplant candidates will review a set of suggested talking points and an example script to guide discussion of potential living donation with members of their network. 25% of participants will be assigned to each of the following factorial experimental groups: no intervention, search intervention only, script intervention only, or both search and script intervention.There are two interventions randomly assigned to participants in a factorial experimental design. The first intervention is the search intervention. In addition to the candidate survey, transplant candidates assigned to this intervention will be given information about the statistical likelihood that each member of their social network will be free of contraindications for living kidney donation. The second intervention is the script intervention, where in addition to the survey, transplant candidates will review a set of suggested talking points and an example script to guide discussion of potential living donation with members of their network. 25% of participants will be assigned to each of the following factorial experimental groups: no intervention, search intervention only, script intervention only, or both search and script intervention.
Masking:
None (Open Label)
Primary Purpose:
Health Services Research
Official Title:
Social Network Interventions to Reduce Race Disparities in Living Kidney Donation
Actual Study Start Date :
Oct 12, 2021
Anticipated Primary Completion Date :
Apr 1, 2024
Anticipated Study Completion Date :
Apr 1, 2024

Arms and Interventions

Arm Intervention/Treatment
No Intervention: No intervention

This group will only complete study survey and refer members of their family and social network for participation in a web survey.

Experimental: Script Intervention

This group will complete the survey, refer members of their family and social network for participation in a web survey, and review a set of suggested talking points and an example script to guide discussion of potential living donation with members of their network.

Behavioral: Script Intervention
This intervention provides language to participants to allow them to discuss kidney transplantation with their social network.

Experimental: Search Intervention

This group will complete the candidate survey, refer members of their family and social network for participation in a web survey, and be given information about the statistical likelihood that each member of their social network will be free of contraindications for living kidney donation.

Behavioral: Search Intervention
This group will complete the candidate survey, refer members of their family and social network for participation in a web survey, and be given information about the statistical likelihood that each member of their social network will be free of contraindications for living kidney donation.

Experimental: Both Search and Script Intervention

This group will complete the candidate survey, refer members of their family and social network for participation in a web survey, be given information about the statistical likelihood that each member of their social network will be free of contraindications for living kidney donation, and review a set of suggested talking points and an example script to guide discussion of potential living donation with members of their network.

Behavioral: Script Intervention
This intervention provides language to participants to allow them to discuss kidney transplantation with their social network.

Behavioral: Search Intervention
This group will complete the candidate survey, refer members of their family and social network for participation in a web survey, and be given information about the statistical likelihood that each member of their social network will be free of contraindications for living kidney donation.

Outcome Measures

Primary Outcome Measures

  1. Received a living donor kidney transplant [up to 3 years]

    Living donor kidney transplant received by patient

  2. Received a deceased donor kidney transplant [up to 3 years]

    Deceased donor kidney transplant received by patient

  3. Death [up to 3 years]

    Patient died during the follow-up period

  4. Completed living kidney donor screening questionnaires [up to 3 years]

    Number of completed living kidney donation screening questionnaires completed for patient

  5. Preliminary approval from living kidney donor screening questionnaires [up to 3 years]

    Number of completed living kidney donor screening that received preliminary approval for patient

  6. Completed living kidney donor evaluations [up to 3 years]

    Number of living kidney donor evaluations completed for patient

  7. Approvals for living kidney donor candidacy [up to 3 years]

    Number of completed living kidney donor evaluations that resulted in approved living kidney donor candidacy for patient

Secondary Outcome Measures

  1. Preference for living kidney donor [Immediate]

    A set of survey questions asked both before and after the intervention, to assess intermediate attitude outcomes regarding preference for living kidney donor

  2. Concerns about living kidney donation [Immediate]

    A set of survey questions asked both before and after the intervention, to assess intermediate attitude outcomes regarding concerns for living kidney donation

  3. Living donor kidney transplant willingness [Immediate]

    A set of survey questions asked both before and after the intervention, to assess intermediate attitude outcomes regarding living donor kidney transplant willingness

  4. Self-rated kidney transplant knowledge [Immediate]

    Respondent is asked to rate their level of knowledge related to kidney transplantation.

  5. Trust in medical institutions [Immediate]

    Respondent is asked to rate their trust in medical institutions.

  6. Religious views' effect on kidney transplant willingness [Immediate]

    Respondent is asked how strongly they agree that their religious views affect their willingness to pursue a kidney transplant.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Are KT candidates at the University of Pennsylvania or University of Alabama-Birmingham OR were identified by KT candidate from the University of Pennsylvania or University of Alabama-Birmingham as a network member

  • Are adults aged 18 or older

  • Are able and willing to consent to participation in the survey

Exclusion Criteria:
  • Person is not a KT candidate at University of Pennsylvania or University of Alabama-Birmingham OR was NOT identified by KT candidate from University of Pennsylvania or University of Alabama-Birmingham as a network member

  • Individuals who are not yet 18

  • Participant does not speak English

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Alabama-Birmingham Birmingham Alabama United States 35233
2 Penn Medicine-- University of Pennsylvania Philadelphia Pennsylvania United States 19104

Sponsors and Collaborators

  • Penn State University
  • University of Pennsylvania
  • University of Alabama at Birmingham

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Jonathan Daw, Associate Professor of Sociology and Demography, Penn State University
ClinicalTrials.gov Identifier:
NCT05255757
Other Study ID Numbers:
  • 849197
First Posted:
Feb 25, 2022
Last Update Posted:
Jul 15, 2022
Last Verified:
Jul 1, 2022
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
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 15, 2022