MedPath

Expanding Live Donor Kidney Transplantation Through Advocacy Training and Social Media

Not Applicable
Active, not recruiting
Conditions
Kidney Diseases
Kidney Failure
Interventions
Behavioral: Live Donor Champion + Facebook App
Behavioral: Facebook App
Registration Number
NCT03099434
Lead Sponsor
Johns Hopkins University
Brief Summary

This pilot study will be a clinical trial to test the feasibility and effectiveness of an educational intervention and a mobile health intervention in adults with end stage renal disease (ESRD) who have not yet identified a potential live donor.

Detailed Description

Transplant candidates are hesitant to discuss their illness and the difficulties associated with dialysis, and are therefore reluctant to pursue live donor kidney transplant (LDKT). The investigators will conduct a prospective 3-arm randomized controlled trial with two novel interventions to increase live donation. Arm 1 includes LDC program and the Facebook app, Arm 2 includes just the Facebook app, and Arm 3 includes standard of care. The investigators primary objective is to demonstrate the the effectiveness of these interventions in increasing live donor transplantation rates for candidates with no prior potential live donor.

Recruitment & Eligibility

Status
ACTIVE_NOT_RECRUITING
Sex
All
Target Recruitment
775
Inclusion Criteria
  • Kidney transplant candidates aged≥18 added to the waitlist in the last year with no potential live donors are eligible.
  • If there is an individual willing to donate, but the candidate is unwilling to consider this option or this particular individual, the candidate is eligible for the trial and may still benefit from identification of new donors or increased comfort accepting donation from others.
  • Participants at Johns Hopkins University or University of Alabama must speak English. Participants at Northwestern University must speak English or Spanish.
Exclusion Criteria
  • Candidates with live donors currently under evaluation for donation will be excluded.
  • Those with a previous kidney transplant will be excluded

Study & Design

Study Type
INTERVENTIONAL
Study Design
FACTORIAL
Arm && Interventions
GroupInterventionDescription
Live Donor Champion + Facebook AppLive Donor Champion + Facebook AppThe LDC program consists of 6 monthly sessions of approx. 1 hour each. Each LDC session is led by a transplant physician or clinical coordinator. LDC sessions incorporate formal didactics, active-participant learning, personal stories, moderated group discussions, role-playing, and other skill-building exercises. LDC sessions are as follows: 1) education about ESRD, KT, and LDKT 2) communication skills building 3) Exploring social networks 4) sharing successful donor and recipient stories 5) encouraging candidate self-efficacy. At session 3, the the Facebook app will be incorporated and given to candidates. The Facebook app provides step-by-step instructions for creating a Facebook post that details each waitlist candidate's struggle with ESRD and their need for a live donor. The post is then uploaded to Facebook so it can be shared with the candidate's Facebook social network.
Facebook AppFacebook AppThe Facebook app provides step-by-step instructions for creating a Facebook post that details each waitlist candidate's struggle with ESRD and their need for a live donor. The post is then uploaded to Facebook so it can be shared with the candidate's Facebook social network. The Facebook App prompts users with specific questions to create a narrative. Links to supplemental resources are auto-populated into the post to provide anyone that views the post with vetted information about the risks, benefits, and process of live donation. Candidates using the Facebook app attend one focus group session held at the transplant center where they are provided with verbal instructions and visual demonstrations of installation and use of the Facebook app.
Primary Outcome Measures
NameTimeMethod
Live donor kidney transplantationwithin 1 year of enrollment

Live donor kidney transplantation within one year of enrollment into the study will be the primary outcome and will be collected/identified through electronic medical record system.

Secondary Outcome Measures
NameTimeMethod
Live Donor Inquirieswithin 1 year of enrollment

Live Donor Inquiries on behalf of candidates will be the secondary outcome and will be collected/identified through electronic medical record system.

knowledge of live donationwithin 6 months of enrollment

knowledge of live donation of transplant candidates will be collected during the survey.

comfort initiating conversationswithin 6 months of enrollment

comfort initiating conversations with others about live donation will be collected during the survey.

Trial Locations

Locations (2)

Johns Hopkins University

🇺🇸

Baltimore, Maryland, United States

Northwestern University

🇺🇸

Evanston, Illinois, United States

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