Evaluation of a Website on Living Kidney Donation for Hispanics

Sponsor
Northwestern University (Other)
Overall Status
Completed
CT.gov ID
NCT01859871
Collaborator
(none)
123
2
2
28
61.5
2.2

Study Details

Study Description

Brief Summary

The purpose of this study is to increase understanding about living kidney donation (LKD) among Hispanic/Latino patients and public by increasing knowledge and positive attitudes about LKD. Improving Hispanics' understanding about LKD will ensure that Hispanic patients and public are fully informed of the treatment options for End Stage Kidney Disease.

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

Detailed Description

The shortage of kidneys for transplantation, and ethnic disparities in living kidney donation rates are major public health problems. Hispanics need more kidney transplants, yet receive fewer living donor kidney transplants than they need. Factors known to contribute to Hispanics' low rates of living donation kidney transplantation include cultural beliefs, lack of knowledge, and negative attitudes about living kidney donation. Web-based interventions are promising as Hispanics are using the Internet at increasingly greater rates. However, few websites about transplantation are tailored to potential Hispanic kidney transplant candidates or the Hispanic community. This study aims to develop, test, and evaluate the effectiveness of a bilingual web-based educational resource targeted to Hispanic patients and the public, which can serve as a low-cost, convenient, and culturally competent tool to enhance knowledge about living kidney donation. Improving Hispanics' understanding about living kidney donation will promote their autonomy and self-determination by helping to ensure that Hispanic patients and public are fully informed of the treatment options for end-stage kidney disease.

Study Design

Study Type:
Interventional
Actual Enrollment :
123 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Investigator)
Primary Purpose:
Health Services Research
Official Title:
Evaluation of a Culturally Competent Website on Living Kidney Donation for Hispanics
Study Start Date :
May 1, 2013
Actual Primary Completion Date :
Feb 1, 2015
Actual Study Completion Date :
Sep 1, 2015

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control Arm

Study participants will take the self-administered pre-test and receive the standard of care. After taking the pre-test, control arm participants will be done with study participation for that day and will attend the transplant center's education sessions. All participants will receive a letter and follow-up call at about two weeks later to schedule the final survey. They will take a final survey via telephone about 3 weeks later. The final survey includes the same topics as the pre-test. They will receive a thank you letter and gift card by mail after completing the final survey.

Experimental: Website Intervention

Navigate website plus standard of care

Behavioral: Website Intervention
Study participants will take the self-administered pre-test in the intervention arm and will be introduced to the website to inform the public of various topics concerning end-stage kidney disease and kidney transplantation. Few websites about transplantation are tailored to potential Hispanic kidney transplant candidates or the Hispanic community. This website is designed to fill the void and be an effective bilingual web-based educational resource targeted to Hispanic patients and public which can serve as a culturally competent tool to enhance knowledge and attitudes about living kidney donation.

Outcome Measures

Primary Outcome Measures

  1. Knowledge about Living Kidney Donation [3 weeks]

    Will assess change in knowledge and positive attitudes about risks, benefits, processes, and cultural factors associated with living kidney donation over time, and their associations with participant characteristics (i.e., age, literacy).

Secondary Outcome Measures

  1. Website use and satisfaction [3 weeks]

    Will assess satisfaction and use of website 3 weeks after enrollment.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Adults (age ≥ 18 years)

  • Hispanics/Latinos

  • ESRD patients who are scheduled to attend each participating transplant center's education sessions. Sessions mark the first phase of evaluation in order for patients to get wait listed for a transplant or for others to become a living kidney donor.

  • Family and friends who accompany patients to the transplant center.

  • Identification as Hispanic/Latino.

  • Ability to come to Northwestern 3 hours prior to the scheduled education session.

  • Ability to read. Reading ability will be assessed using the 5-point Likert scale question validated in English and Spanish:13 "How often do you need to have someone help you when you read instructions, pamphlets, or other written material from your doctor or pharmacy?" People will be included if they reply 1-Never or 2-Rarely.

Exclusion Criteria:
  • Non-identification as Hispanic/Latino.

  • Inability to come to Northwestern 3 hours prior to the scheduled education session.

  • Individuals who are not able to read Spanish or English. People will be excluded if they reply 3-Sometimes, 4-Often, and 5-Always to the question, "How often do you need to have someone help you when you read instructions, pamphlets, or other written material from your doctor or pharmacy?" .

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of California, Davis Davis California United States 95817
2 Northwestern Memorial Hospital (NMH) Chicago Illinois United States 60611

Sponsors and Collaborators

  • Northwestern University

Investigators

  • Principal Investigator: Elisa Gordon, PhD, MPH, Northwestern University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Elisa Gordon, Principal Investigator, Northwestern University
ClinicalTrials.gov Identifier:
NCT01859871
Other Study ID Numbers:
  • R39OT22059
First Posted:
May 22, 2013
Last Update Posted:
Nov 20, 2015
Last Verified:
Nov 1, 2015
Keywords provided by Elisa Gordon, Principal Investigator, Northwestern University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 20, 2015