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Health Education & Behavior
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Article

Retention in a Breast Cancer Risk Information Trial: Motivations of a Population-Based Sample of Women

Kiley Ariail, MPH1, Carolyn (Cindy) Watts, PhD2, Deborah J. Bowen, PhD3*

1 Oregon Department of Human Services, Genetics Program, Portland.
2 University of Washington, Department of Health Services, Seattle.
3 Fred Hutchinson Cancer Research Center, Seattle, Washington.

* To whom correspondence should be addressed. E-mail: dbowen{at}fhcrc.org..


  Abstract

A better understanding of factors influencing retention in breast cancer risk education and prevention programs can improve the design and effectiveness of such programs. Such information may also be useful to researchers seeking to maximize full retention in research trials involving low risk and low perceived benefit by the participants. These data are from a population-based study of 481 women from the Seattle, Washington, area, with diverse levels of breast cancer risk. This study sought to describe motivations for retention, to relate motivation variables to demographic characteristics, and to evaluate predictors of retention. Increasing age predicted study assessment completion, and both cancer worry and White ethnicity predicted intervention retention.

Key Words: recruitment, participation in clinical trials

First published on July 21, 2006, doi:10.1177/1090198106288493

Health Education & Behavior 2006;33:591.

A more recent version of this article appeared on October 1, 2006

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