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OpenTrials
Completed

NCT Number: NCT01261910

Enhancing Education Regarding Living Donor Transplant Among Kidney Transplant Candidates

The primary purpose of this study is to test different methods by which kidney transplant centers can educate potential transplant candidates about living donor kidney transplant (LDKT).

The most effective ways to educate kidney transplant candidates about LDKT remain unclear. The goal is to determine, among a diverse cohort of potential kidney transplant candidates, whether a transplant center-based intervention will increase understanding of the opportunities for and process, risks, and benefits of living kidney donation and LDKT. The investigators hypothesize that kidney transplant candidates' understanding of living kidney donation and LDKT will be increased by interventions implemented at the transplant center on the day of transplant evaluation.

The investigators propose a single-center, 2-arm, cluster-randomized, controlled trial to compare the effects of two educational strategies upon transplant candidates' understanding of living kidney donation and LDKT:

1. Usual transplant education implemented by the transplant center, on the day of the transplant evaluation (standard care); and 2. Intensive initial transplant education implemented on the day of the transplant evaluation.

Intensive initial transplant education will utilize videos of living donors' experiences as well as a session with a trained Transplant Educator, who will focus upon living donation education. One week after the transplant evaluation day and 3 months later, the investigators will assess transplant candidates' knowledge of LDKT (using questionnaires), identify correlates of increased understanding of LDKT, and assess racial/ethnic differences in the understanding of LDKT.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Appear for initial kidney transplant evaluation at Saint Barnabas Medical Center
  • 18 years of age or older
  • Able to provide informed consent
  • Able to speak, hear, and understand English

Exclusion criteria

Treatment and study plan

Intensive initial education

Behavioral

Participants will (1) view a video, brochure, and fact sheet regarding living kidney donation, and (2) discuss the videos and materials with a transplant educator, in-person.

Primary outcomes

  1. Knowledge and understanding of the opportunities for and process, risks, and benefits of living kidney donation and LDKT

    Time frame: Up to 1 week after the transplant education day

Secondary outcomes

  1. Knowledge and understanding of the opportunities for and process, risks, and benefits of living kidney donation and LDKT

    Time frame: Three months after the transplant education day

  2. Attitudes, confidence, and opinions regarding living kidney donation and LDKT

    Time frame: (1) Up to 1 week after the transplant education day, and (2) Three months after the transplant education day

  3. Changes in knowledge/understanding and attitudes/confidence/opinions regarding living kidney donation and LDKT

    Time frame: (1) Up to 1 week after the transplant education day, and (2) Three months after the transplant education day, compared to prior to the transplant evaluation day (baseline)

Sponsors and collaborators

Lead sponsor

St. Barnabas Medical Center

Other

Collaborators

  • Health Resources and Services Administration (HRSA)
  • University of Medicine and Dentistry of New Jersey

Registry information

Important dates

Study start
2010
Primary completion
2013
Study completion
2013
First posted
Dec 17, 2010
Registry last updated
Jul 28, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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