Literature DB >> 31890053

Sexual and gender minority youth's perspectives on sharing de-identified data in sexual health and HIV prevention research.

Margaret Matson1, Kathryn Macapagal1,2, Ashley Kraus1, Ryan Coventry1, Emily Bettin1, Celia B Fisher3, Brian Mustanski1,2.   

Abstract

Funding agencies encourage and sometimes require data sharing. However, there is limited empirical research on participant perspectives on sharing de-identified data from research on sensitive topics (e.g., HIV, sexual health) with other researchers, and virtually none from adolescents or sexual and gender minority (SGM) participants. SGM teens (N = 197) ages 14-17 completed an online survey with multiple choice and open-ended items assessing perspectives toward sharing survey responses and blood samples from sexual health and HIV testing studies with other researchers. SGM youth were willing to share data but frequently cited confidentiality and privacy concerns, including fears about parents finding out about their identities even after de-identification was explained. Researchers need to ensure youth understand explanations of data security protections in order to make well-informed decisions about participating in research.

Entities:  

Keywords:  HIV prevention; adolescents; data sharing; gender identity; participant perspectives; research ethics; sexual orientation

Year:  2019        PMID: 31890053      PMCID: PMC6936765          DOI: 10.1007/s13178-018-0372-7

Source DB:  PubMed          Journal:  Sex Res Social Policy        ISSN: 1553-6610


  33 in total

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Authors:  Celia B Fisher
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6.  African Americans' views on research and the Tuskegee Syphilis Study.

Authors:  V S Freimuth; S C Quinn; S B Thomas; G Cole; E Zook; T Duncan
Journal:  Soc Sci Med       Date:  2001-03       Impact factor: 4.634

7.  Self-Consent for HIV Prevention Research Involving Sexual and Gender Minority Youth: Reducing Barriers Through Evidence-Based Ethics.

Authors:  Celia B Fisher; Miriam R Arbeit; Melissa S Dumont; Kathryn Macapagal; Brian Mustanski
Journal:  J Empir Res Hum Res Ethics       Date:  2016-03-07       Impact factor: 1.742

8.  Ethical implications of including children in a large biobank for genetic-epidemiologic research: a qualitative study of public opinion.

Authors:  David Kaufman; Gail Geller; Lisa Leroy; Juli Murphy; Joan Scott; Kathy Hudson
Journal:  Am J Med Genet C Semin Med Genet       Date:  2008-02-15       Impact factor: 3.908

9.  Genomics, Big Data, and Broad Consent: a New Ethics Frontier for Prevention Science.

Authors:  Celia B Fisher; Deborah M Layman
Journal:  Prev Sci       Date:  2018-10

10.  "Free Testing and PrEP without Outing Myself to Parents:" Motivation to participate in oral and injectable PrEP clinical trials among adolescent men who have sex with men.

Authors:  Celia B Fisher; Adam L Fried; Leah Ibrahim Puri; Kathryn Macapagal; Brian Mustanski
Journal:  PLoS One       Date:  2018-07-25       Impact factor: 3.240

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2.  Perceived risks and amelioration of harm in research using mobile technology to support antiretroviral therapy adherence in the context of methamphetamine use: a focus group study among minorities living with HIV.

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Journal:  Arch Sex Behav       Date:  2021-11-15

4.  What influences a person's willingness to share health information for both direct care and uses beyond direct care? Findings from a focus group study in Ireland.

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  4 in total

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