Assessing the Awareness of and Willingness to Participate in Cancer Clinical Trials Among Immigrant Latinos
- 469 Downloads
Clinical trials are considered the gold standard of evidence about the efficacy of cancer prevention, early detection, and treatment interventions. A paucity of data exists on determinants of clinical trial participation in the growing US Latino population despite poor cancer outcomes in this group. This study seeks to describe correlates of awareness of and willingness to participate in clinical trials among largely Central, North, and South American Latinos using safety-net clinics. Between June 2007 and November 2008, we conducted an interviewer-administered, Spanish-language cross-sectional survey (n = 944). Logistic regression was used to assess effects of health information sources and psychosocial variables on awareness of and intention to participate in clinical trials. Analyses were completed in spring 2010. While only 48% knew what a clinical trial was, when explained, 65% indicated a willingness to participate. Providers were the most common source of health information. Use of Internet for health information, trust in health information, and higher education each independently increased the odds of clinical trial awareness, but obtaining information from providers did not. Contacting the Cancer Information Service and psychosocial factors were each independently associated with intent to join a clinical trial, while demographic factors were not. Information channels such as the Internet may be effective in conveying clinical trial information to Latinos. Providers being cited as the most common source of health information but not being associated with knowledge about or intent to participate in trials suggests a missed opportunity for communication to this population.
KeywordsClinical trial awareness Clinical trial participation Latinos Informational channels Health disparities
This research was funded by a grant from the National Cancer Institute (U01 CA114593‐03S3) as part of the Latin American Cancer Research Coalition (LACRC). This research was also supported by NCI grant KO5 CA96940 (JM) and the Biostatistics and Bioinformatics Shared Resource at Lombardi Comprehensive Cancer Center under NCI grant P30CA51008 (AN, GL).
- 2.National Institutes of Health. (1994). NIH guidelines on the inclusion of women and minorities as subjects in clinical research. Retrieved from http://www.grants.nih.gov/grants/guide/notice-files/not94-100.html.
- 5.US Census Bureau. (2010). American community survey demographic and housing estimates: 2005–2007. Retrieved from http://www.census.gov/acs/.
- 6.American Cancer Society. (2009). Cancer facts and figures for Hispanics/Latinos 2009–2011. Retrieved from http://www.cancer.org/Research/CancerFactsFigures/CancerFactsFiguresforHispanicsLatinos/index.
- 24.Bazargan, M., Bazargan, S. H., Calderon, J. L., Husaini, B. A., & Baker, R. S. (2003). Mammography screening and breast self-examination among minority women in public housing projects: The impact of physician recommendation. Cell and Molecular Biology, 49(8), 1213–1218.Google Scholar
- 36.Altman, S., & Lewin, M. E. (Eds.). (2000). America’s health care safety net: Intact but endangered. Retrieved from http://www.books.nap.edu/openbook.php?record_id=9612&page=R1.