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临床试验/NCT03013829
NCT03013829已完成不适用

Kidney Paired Donation: A Randomized Trial to Increase Knowledge and Informed Decision-Making

Beth Israel Deaconess Medical Center6 个研究点 分布在 1 个国家目标入组 588 人开始时间: 2018年6月26日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
588
试验地点
6
主要终点
Living Donation and KPD Knowledge

研究概览

简要总结

The purpose of this study is to evaluate the effectiveness of a targeted educational approach designed to increase knowledge about the risks and benefits of living donation generally and KPD (Kidney Paired Donation) specifically, enhance KPD self-efficacy, reduce KPD concerns, and facilitate informed decision-making about KPD among potential live kidney donor and kidney transplant patients.

详细描述

The investigators will conduct a randomized controlled trial (RCT) to examine the effectiveness of a video-based KPD education intervention to improve knowledge, self-efficacy, concerns, and informed decision-making about KPD among potential live kidney donor and kidney transplant patients.

There will be equal allocation of LKDs and intended recipients to both KPD education conditions: (1) Usual Care (UC) group and (2) UC plus video-based KPD education group. All enrolled LKDs and intended recipients will complete a baseline survey and another survey 2 weeks post-intervention. Additionally, follow-up data will be gathered on KPD decision-making, participation, and reasons for non-participation at 3 months post-intervention.

Settings and target population:

The study will be conducted at three kidney transplant programs in the United States: Beth Israel Deaconess Medical Center (BIDMC; Boston, MA), the Medical University of South Carolina (MUSC; Charleston, SC), and Erie County Medical Center (ECMC; Buffalo, NY). BIDMC will act as the coordinating center for this study and will be responsible for study design, oversite, reporting, updates, and final data analysis. MUSC and ECMC will rely on the CCI at BIDMC for review. This study will target potential LKDs and their intended recipients.

Randomization:

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Investigator)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Speaks English or Spanish
  • Completed the initial living donation health screening
  • Transplant Candidates
  • Speaks English or Spanish
  • On that transplant waitlist (active or inactive)

排除标准

  • Non-directed (i.e., anonymous) potential LKDs
  • Previously undergone donor evaluation
  • Participation in another study to increase knowledge about living donation/LDK
  • Transplant Candidates
  • Had a prior LDKT
  • Previously enrolled in a KPD program
  • Previous or current participation in another study to increase knowledge about living donation/LDKT
  • Listed for a liver

结局指标

主要结局

Living Donation and KPD Knowledge

时间窗: three months post-intervention

A questionnaire will be used to assess living donation and KPD knowledge.

次要结局

  • Living Donation and KPD Concerns(2 weeks post-intervention)
  • Living Donation and KPD Self-Efficacy(2 weeks post-intervention)
  • Living Donation and KPD Discussions(2 weeks post-intervention)
  • Informed Decision-Making(2 weeks post-intervention)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

James Rodrigue

Vice Chair of Clinical Research

Beth Israel Deaconess Medical Center

研究点 (6)

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