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Optimizing Kidney Transplant Informed Consent

Primary Purpose

End-stage Kidney Disease

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Inform Me: web-based education tool
Sponsored by
Northwestern University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for End-stage Kidney Disease focused on measuring Kidney transplantation, Increased risk donor kidneys, Kidney donation, Organ donation, Human Immunodeficiency Virus, Hepatitis B, Hepatitis C, Infectious disease, Disease transmission, Centers for Disease Control (CDC), Web-based intervention

Eligibility Criteria

21 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • English-speaking
  • 21 years or older
  • Kidney Transplant candidates eligible: 1) completed the first phase of transplant evaluation education, and 2) wait-listed patients expected to receive a transplant within the next 6 months, returning for re-evaluation.

Exclusion Criteria:

  • No special classes of study participants, including fetuses, neonates, prisoners, institutionalized individuals, or other vulnerable populations will be included in the proposed study. Although pregnant women will be eligible for participation in the study, they are unlikely to be selected for kidney transplantation.

Sites / Locations

  • University of Alabama at Birmingham
  • Northwestern Memorial Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Inform Me: web-based education tool

Control Standard of Care

Arm Description

Intervention will receive the standard of care, the Inform Me intervention, a post-test evaluation, and 1 week recall test.

This group receives standard of care with a post test.

Outcomes

Primary Outcome Measures

Knowledge of increased risk donor kidney transplants
Assess knowledge of increased risk donor kidneys

Secondary Outcome Measures

Willingness to accept an increased risk donor kidney transplant
Willingness to accept an increased risk donor kidney.

Full Information

First Posted
May 20, 2013
Last Updated
November 18, 2015
Sponsor
Northwestern University
Collaborators
University of Alabama at Birmingham
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1. Study Identification

Unique Protocol Identification Number
NCT01859884
Brief Title
Optimizing Kidney Transplant Informed Consent
Official Title
Optimizing Kidney Transplant Patients' Informed Consent for Increased Risk Donors
Study Type
Interventional

2. Study Status

Record Verification Date
November 2015
Overall Recruitment Status
Completed
Study Start Date
October 2013 (undefined)
Primary Completion Date
December 2014 (Actual)
Study Completion Date
November 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Northwestern University
Collaborators
University of Alabama at Birmingham

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The objective of this study is to evaluate kidney transplant candidates' comprehension about increased risk donor kidneys necessary for informed consent. We have developed a web-based tool that educates and assesses candidates' comprehension (Inform Me), as a supplement to current informed consent processes. We will then compare the effectiveness of the current informed consent processes supplemented by Inform Me, with the current consent processes alone for kidney transplant.
Detailed Description
The shortage of kidneys for kidney transplantation results in almost 10,000 deaths per year in the United States. One strategy to increase the number of available kidneys is to offer kidney transplant candidates kidneys that come from donors who have an increased risk of transmission of human immunodeficiency virus (HIV), Hepatitis B and Hepatitis C. Increased risk kidney donors are defined as those who have engaged in behaviors associated with an increased risk of HIV, Hepatitis B, and Hepatitis C, and comprise approximately 9% of all US deceased organ donors. The Organ Procurement and Transplantation Network policy mandated informed consent from recipients who accept increased risk kidneys. The objective of this study is to increase study participants' comprehension about increased risk donor kidneys necessary for informed consent. To accomplish this objective, we will develop a web-based tool that educates and assesses participants' comprehension (Inform Me), as a supplement to current informed consent processes. We will then compare the effectiveness of the current informed consent processes supplemented by Inform Me, with the current consent processes alone. The tool will utilize health information technology to deliver information about the definition of, risks, benefits, and alternatives to using increased risk donor kidneys via a web-based application. Computer adaptive learning will personalize information presented to each candidate according to his/her comprehension levels in interactive chapters to increase comprehension. Inform Me will facilitate nurses' primary role as patient educators.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
End-stage Kidney Disease
Keywords
Kidney transplantation, Increased risk donor kidneys, Kidney donation, Organ donation, Human Immunodeficiency Virus, Hepatitis B, Hepatitis C, Infectious disease, Disease transmission, Centers for Disease Control (CDC), Web-based intervention

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
288 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Inform Me: web-based education tool
Arm Type
Experimental
Arm Description
Intervention will receive the standard of care, the Inform Me intervention, a post-test evaluation, and 1 week recall test.
Arm Title
Control Standard of Care
Arm Type
No Intervention
Arm Description
This group receives standard of care with a post test.
Intervention Type
Behavioral
Intervention Name(s)
Inform Me: web-based education tool
Intervention Description
The purpose of Inform Me is to help kidney transplant candidates understand what kidneys from increased risk donors are and describes the risks and benefits of accepting and refusing a kidney from an increased risk donor. Increased risk donors are donors who engaged in behaviors that increase their chances of having: Human Immunodeficiency Virus, Hepatitis B Virus , Hepatitis C Virus. Inform Me focuses only on increased risk donor kidneys. Inform Me aims to prepare patients to make a decision with their transplant team to accept or to refuse a kidney from an increased risk donor. Inform Me does not try to convince patients to accept or refuse a kidney from increased risk donors.
Primary Outcome Measure Information:
Title
Knowledge of increased risk donor kidney transplants
Description
Assess knowledge of increased risk donor kidneys
Time Frame
1 week
Secondary Outcome Measure Information:
Title
Willingness to accept an increased risk donor kidney transplant
Description
Willingness to accept an increased risk donor kidney.
Time Frame
1 week
Other Pre-specified Outcome Measures:
Title
Decisional conflict
Description
Will measure difficulty in treatment decision-making.
Time Frame
1 week
Title
Satisfaction with the informed consent process
Description
Assess decision-making quality, decision satisfaction, and perception of information.
Time Frame
1 week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: English-speaking 21 years or older Kidney Transplant candidates eligible: 1) completed the first phase of transplant evaluation education, and 2) wait-listed patients expected to receive a transplant within the next 6 months, returning for re-evaluation. Exclusion Criteria: No special classes of study participants, including fetuses, neonates, prisoners, institutionalized individuals, or other vulnerable populations will be included in the proposed study. Although pregnant women will be eligible for participation in the study, they are unlikely to be selected for kidney transplantation.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Elisa Gordon, PhD, MPH
Organizational Affiliation
Northwestern University
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Alabama at Birmingham
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35233
Country
United States
Facility Name
Northwestern Memorial Hospital
City
Chicago
State/Province
Illinois
ZIP/Postal Code
60611
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
27463536
Citation
Gordon EJ, Sohn MW, Chang CH, McNatt G, Vera K, Beauvais N, Warren E, Mannon RB, Ison MG. Effect of a Mobile Web App on Kidney Transplant Candidates' Knowledge About Increased Risk Donor Kidneys: A Randomized Controlled Trial. Transplantation. 2017 Jun;101(6):1167-1176. doi: 10.1097/TP.0000000000001273.
Results Reference
derived

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Optimizing Kidney Transplant Informed Consent

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