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Beyond community engagement: perspectives on the meaningful involvement of people with HIV and affected communities (MIPA) in HIV cure research in The Netherlands.
Marcos, Tamika A; Jonas, Kai J; Noorman, Maaike A J; den Daas, Chantal; de Wit, John B F; Stutterheim, Sarah E.
Afiliação
  • Marcos TA; Department of Work and Social Psychology, Maastricht University, Maastricht, the Netherlands.
  • Jonas KJ; Department of Work and Social Psychology, Maastricht University, Maastricht, the Netherlands.
  • Noorman MAJ; Department of Interdisciplinary Social Science, Utrecht University, Utrecht, The Netherlands.
  • den Daas C; Institute of Applied Health Sciences, Health Psychology Group, University of Aberdeen, Aberdeen, UK.
  • de Wit JBF; Department of Interdisciplinary Social Science, Utrecht University, Utrecht, The Netherlands.
  • Stutterheim SE; Department of Health Promotion and Care and Public Health Research Institute, Maastricht University, Maastricht, the Netherlands.
HIV Res Clin Pract ; 25(1): 2335454, 2024 Dec.
Article em En | MEDLINE | ID: mdl-38577964
ABSTRACT

BACKGROUND:

Meaningful involvement of people with HIV and affected communities in HIV cure research is essential to ensuring that cure research efforts are conducted transparently, socially justly, and ethically. This study set out to investigate how people with HIV and affected communities are involved in cure research in the Netherlands and explore what can be done to optimize involvement and engagement.

METHODS:

Eighty-five semi-structured online, telephone, and face-to-face interviews were conducted with people with HIV (N = 30), key populations (N = 35), and key informants (KI; N = 20) in the field of HIV. The interviews were analyzed using reflexive thematic analysis.

RESULTS:

Awareness of the meaningful involvement of people with HIV (MIPA) efforts was low among people with HIV and key populations, which contrasted with KI, who exhibited greater awareness. People with HIV and KI emphasized the importance of MIPA in ensuring the representation of lived experiences in HIV cure research and fostering trust between communities and researchers. Practical implementations of MIPA were unclear, ultimately resulting in difficulties defining MIPA beyond clinical trial participation. People with HIV and key populations also doubted their skills and self-efficacy to make meaningful contributions when confronted with involvement beyond participating in research and clinical trials.

CONCLUSIONS:

MIPA is crucial for improving the quality, transparency, and ethical conduct of HIV cure research. It emphasizes the need for increased awareness and funding, standardized guidelines to ensure meaningful involvement, and combat tokenism and misconceptions.
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Base de dados: MEDLINE Assunto principal: Infecções por HIV Idioma: En Ano de publicação: 2024 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Infecções por HIV Idioma: En Ano de publicação: 2024 Tipo de documento: Article