Literature DB >> 25825819

Demographic differences in willingness to provide broad and narrow consent for biobank research.

Altovise T Ewing1, Lori A H Erby, Juli Bollinger, Eva Tetteyfio, Luisel J Ricks-Santi, David Kaufman.   

Abstract

PURPOSE: This study examined acceptability of two biobank consent models and evaluated the impact of beliefs about privacy and genetic safeguards on acceptance.
METHODS: U.S. adults surveyed online in English and Spanish were randomly assigned to one of two scenarios examining acceptance of broad consent (n=1528), or narrow consent (n=1533).
RESULTS: Overall, willingness to provide broad (76%) and narrow (74%) consents were similar. African Americans were as likely as white non-Hispanics to accept narrow consent (72% vs. 77%, p=0.35) but significantly less likely to accept broad consent (69% vs. 81%, p=0.004). Education, insurance, and blood donation history were also related to acceptance. Adjusting for beliefs about privacy and policy protections (Genetic Information Nondiscrimination Act, GINA), the effects of the variables were reduced. Respondents who drew comfort from GINA were more likely to support both consent (both p<0.001); those who believed it is impossible to maintain privacy were less likely to find both broad (p=0.04) and narrow models acceptable (p=0.02).
CONCLUSIONS: Choice of consent model matters when engaging diverse populations in biobank research. Beliefs underlying concerns about privacy and genetic protections should be considered when constructing biobank protocols.

Mesh:

Year:  2015        PMID: 25825819      PMCID: PMC4574731          DOI: 10.1089/bio.2014.0032

Source DB:  PubMed          Journal:  Biopreserv Biobank        ISSN: 1947-5543            Impact factor:   2.300


  45 in total

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2.  Potential bias in the bank: what distinguishes refusers, nonresponders and participants in a clinic-based biobank?

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4.  Colorectal cancer knowledge, perceptions, and behaviors in African Americans.

Authors:  Pauline M Green; Beatrice Adderley Kelly
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5.  Strategies for enrollment of African Americans into cancer genetic studies.

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6.  Unexpected findings in the exploration of African American underrepresentation in biospecimen collection and biobanks.

Authors:  Nao Hagiwara; Lisa Berry-Bobovski; Carie Francis; Lauren Ramsey; Robert A Chapman; Terrance L Albrecht
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7.  The case for a US prospective cohort study of genes and environment.

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9.  Consent for genetic research in a general population: the NHANES experience.

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Authors:  Anne Cambon-Thomsen; Pascal Ducournau; Pierre-Antoine Gourraud; David Pontille
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4.  Confidentiality in Biobanking Research: A Comparison of Donor and Nondonor Families' Understanding of Risks.

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7.  Participant views on consent in cancer genetics research: preparing for the precision medicine era.

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Review 10.  Lessons from HeLa Cells: The Ethics and Policy of Biospecimens.

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