Go Back Original Article December, 2017

Minors’ and Young Adults’ Experiences of the Research Consent Process in a Phase II Safety Study of Pre-exposure Prophylaxis for HIV

Abstract

Purpose There is a persistent HIV epidemic among sexual and gender minority adolescents in the U.S. Oral pre-exposure prophylaxis (PrEP) is an efficacious prevention strategy, but not yet approved for minors. Minors' access to biomedical HIV prevention technologies is impeded by the ethical and legal complexities of consent to research participation. We explore autonomous consent and study experiences among minor and adult participants in Project PrEPare, a Phase II safety study of PrEP for HIV prevention. Methods Data for this mixed-methods descriptive study were collected via self-administered web-survey and in-depth telephone interviews in early 2016. Eligible participants were previously enrolled in Project PrEPare. We attempted to contact 191 participants; 74 were reached and expressed interest in participating and 58 enrolled. Results Participants nearly universally felt well informed, understood the study, and freely volunteered with the clear understanding they could withdraw any time. All felt supported by study staff, but a small minority wished for more support during enrollment. Minors were more likely than adults to indicate a wish for more support in decision-making, and adults expressed higher satisfaction with their decision compared to minors. There was no association between elements of consent and Project PrEPare study outcomes. Conclusions Participants had an overwhelmingly positive experience in a Phase II safety study of PrEP for HIV prevention. Some minors wished for more support during the decision-making process, but none consulted their parents about the decision. Our results support the inclusion of decisional supports in consent processes for adolescents, while also protecting their privacy.

Keywords

hiv lgbtq prevention pre-exposure prophylaxis biomedical ethics consent minors young adults research study safety phase ii prep adolescents gender minority oral access participation decision support privacy enrollment satisfaction autonomy clinical trials retention engagement healthcare policy barriers inclusion rights treatment public health sexual identity stigma risk awareness education parental approval confidentiality medical adherence counseling intervention regulatory framework community outreach hiv prevention sexual health legal protections self-efficacy vulnerable populations informed consent risk perception disparities trust empowerment. pre-exposure prophylaxis (prep) biomedical ethics research consent minors’ consent young adults phase ii safety study clinical research adolescent health ethical considerations biomedical research public health healthcare access decision-making clinical trials project prepare legal complexities research participation mixed-methods study healthcare policy medical ethics web-survey patient autonomy public health policy adolescent medicine hiv treatment sexual minority risk reduction medical decision-making health equity human subjects research self-administered survey health policy
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Volume 61
Issue 6
Pages 747–754
ISSN 1879-1972
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