Healthcare Access and Utilization Among Living Kidney Donors

NCT ID: NCT01009125

Last Updated: 2010-06-09

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

600 participants

Study Classification

INTERVENTIONAL

Study Start Date

2010-01-31

Study Completion Date

2010-04-30

Brief Summary

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This is a mailed survey to persons who served as living kidney donors at Saint Barnabas Medical Center. The experimental component of this study (the clinical trial) is a randomized trial of two monetary incentives for the living kidney donors invited to participate in the study. Kidney donors will be randomized to receive one of two incentives in the mailed survey packet: $2 cash vs. $5 cash. The main outcome measure is the response rate to the survey.

Detailed Description

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Conditions

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Organ Donor

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

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$2 cash incentive

Group Type EXPERIMENTAL

$2 cash

Intervention Type OTHER

$2 cash incentive will be included in the mailed survey

$5 cash incentive

Group Type EXPERIMENTAL

$5 cash

Intervention Type OTHER

$5 cash incentive will be included in the mailed survey

Interventions

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$2 cash

$2 cash incentive will be included in the mailed survey

Intervention Type OTHER

$5 cash

$5 cash incentive will be included in the mailed survey

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Persons who donated a living donor kidney at Saint Barnabas Medical Center between January 2000 and December 2006 are eligible to participate

Exclusion Criteria

* Current address outside the continental United States
* Persons who donated a living donor kidney prior to January 2000 or after December 2006
* Persons who indicated they no longer wished to be contacted by Saint Barnabas Medical Center
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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St. Barnabas Medical Center

OTHER

Sponsor Role lead

Responsible Party

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St. Barnabas Medical Center

Principal Investigators

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Francis L Weng, MD

Role: PRINCIPAL_INVESTIGATOR

St. Barnabas Medical Center

Locations

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Saint Barnabas Medical Center

Livingston, New Jersey, United States

Site Status

Countries

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United States

Other Identifiers

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SBMC-2009-40

Identifier Type: -

Identifier Source: org_study_id

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