Literature DB >> 27926908

Community Perceptions of Biobanking Participation: A Qualitative Study among Mexican-Americans in Three Texas Cities.

Natalia I Heredia1, Sarah Krasny, Larkin L Strong, Laura Von Hatten, Lynne Nguyen, Belinda M Reininger, Lorna H McNeill, María E Fernández.   

Abstract

BACKGROUND: Most biospecimens in the US are collected from non-Hispanic Whites, limiting the generalizability of findings. There is a need to increase participation in biobanking among ethnic and racial minorities. The purpose of this study was to use qualitative methods to identify factors that may influence Mexican-American individuals' willingness to participate in biobanking.
METHODS: We conducted 15 focus groups in three Texas cities with Mexican-American individuals, in both Spanish and English.
RESULTS: Lack of knowledge about medical research and biobanks, lack of information about the specifics of biobanking participation, lack of communication of the results, fear of pain or harm, and distrust of the healthcare system or health research were identified as barriers to biobanking participation. Facilitators to participation were altruism, safety, understanding biobanking procedures and purposes, perceived benefits to participation, and culturally appropriate recruitment strategies. Although Mexican-Americans living in Texas are willing to donate biospecimens for altruistic reasons, such as helping society or advancing science, they want more information about what biobanking entails. They want to be assured that participation will not cause them harm and that the research is conducted with good intentions.
CONCLUSION: Results from this study can inform educational materials or interventions to increase Hispanic participation in biobanking.
© 2016 S. Karger AG, Basel.

Entities:  

Keywords:  Biobanking; Biorepository; Biospecimens; Focus groups; Hispanics; Mexican-Americans; Qualitative research

Mesh:

Year:  2016        PMID: 27926908      PMCID: PMC5453816          DOI: 10.1159/000452093

Source DB:  PubMed          Journal:  Public Health Genomics        ISSN: 1662-4246            Impact factor:   2.000


  30 in total

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2.  Formative research on perceptions of biobanking: what community members think.

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3.  Reasons for participating and genetic information needs among racially and ethnically diverse biobank participants: a focus group study.

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4.  Pilot intervention outcomes of an educational program for biospecimen research participation.

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5.  Public opinion about the importance of privacy in biobank research.

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Authors:  Gail E Henderson; R Jean Cadigan; Teresa P Edwards; Ian Conlon; Anders G Nelson; James P Evans; Arlene M Davis; Catherine Zimmer; Bryan J Weiner
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5.  Communicating With Diverse Patients About Participating in a Biobank: A Randomized Multisite Study Comparing Electronic and Face-to-Face Informed Consent Processes.

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10.  A short report of Biosafety and Biobanking: current understanding and knowledge gaps.

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