Living Donation and Kidney Transplantation Information

NCT ID: NCT04285203

Last Updated: 2020-02-26

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

144 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-04-08

Study Completion Date

2020-02-10

Brief Summary

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The purpose of this study is to increase awareness and knowledge regarding the risks and benefits of kidney transplantation and living donation amongst patients seeking kidney transplantation and their family and friends in Buffalo, New York.

Detailed Description

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This prospective randomized parallel controlled trial of kidney transplant candidates receiving and educational intervention and standard of care education versus standard of care education only to improve informed decision making about kidney offers.

Conditions

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Kidney Transplantation

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

DOUBLE

Participants Caregivers

Study Groups

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Educational Video

Participants were exposed to 2 educational videos in addition to standard of care education.

Group Type EXPERIMENTAL

Educational Video Intervention

Intervention Type OTHER

Educational videos

Standard of Care

Participants received standard of care education.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Educational Video Intervention

Educational videos

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* be 18 years or older,
* understand and read English (or have a support person that helps them)
* have acceptable vision to watch videos
* be able to give consent

Exclusion Criteria

* incarcerated
* involved in the former modeling phase of animation development.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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State University of New York at Buffalo

OTHER

Sponsor Role lead

Responsible Party

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Liise Kayler

Clinical Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Liise Kayler, MD

Role: PRINCIPAL_INVESTIGATOR

University at Buffalo

Locations

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Erie County Medical Center

Buffalo, New York, United States

Site Status

Countries

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United States

Other Identifiers

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STUDY00002771

Identifier Type: -

Identifier Source: org_study_id

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