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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01009125
Other study ID # SBMC-2009-40
Secondary ID
Status Completed
Phase N/A
First received November 5, 2009
Last updated June 8, 2010
Start date January 2010
Est. completion date April 2010

Study information

Verified date June 2010
Source St. Barnabas Medical Center
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review Board
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Completed
Enrollment 600
Est. completion date April 2010
Est. primary completion date April 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research


Related Conditions & MeSH terms


Intervention

Other:
$2 cash
$2 cash incentive will be included in the mailed survey
$5 cash
$5 cash incentive will be included in the mailed survey

Locations

Country Name City State
United States Saint Barnabas Medical Center Livingston New Jersey

Sponsors (1)

Lead Sponsor Collaborator
St. Barnabas Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Survey response rate 2 weeks, 2 months (primary), 4 months No
See also
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