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Missing voices

Building women living with HIV’s meaningful engagement in HIV clinical and cure research

Datos Bibliográficos

ID7151280
AutoresSusan C S Chong (Australian Research Centre in Sex, Health and Society, La Trobe University), Susan Chong (0000-0002-9815-3683, La Trobe University, autor de correspondencia), Gene Lim (0000-0001-9083-8883, Australian Research Centre in Sex, Health and Society, La Trobe University), Kirsty Machon (Positive Women Victoria), Heather Mugwagwa (Positive Women Victoria), Jennifer Johnson (0000-0002-2061-4814, Australian Research Centre in Sex, Health and Society, La Trobe University), Roslyn Le Gautier (0000-0002-4012-4126, Australian Research Centre in Sex, Health and Society, La Trobe University), Jennifer Power (0000-0002-6566-3214, Australian Research Centre in Sex, Health and Society, La Trobe University), J Denise Power (0000-0002-9903-6200, La Trobe University)
Año2025
Volumen27
Número9
Páginas1097-1113
Fecha de publicación2025-09-02
Peer ReviewedSí
Open AccessSí
TipoARTICLE
RevistaCulture Health & Sexuality (JOURNAL)
Identificadores de la revistaISSN: 1369-1058 • E-ISSN: 1464-5351
EditorialInforma UK Limited (PUBLISHER • GB)
DOI10.1080/13691058.2024.2408353
PMID39340190
OpenAlexW4402937262
IdiomaEN
Citas recibidas1
Referencias citadas32

Women living with HIV are consistently under-represented in HIV clinical trials, including cure trials. Little is known about how cisgender women living with HIV in Australia perceive HIV cure research, their level of trust in research institutions/staff, and factors salient to participation in HIV cure trials. Semi-structured interviews were conducted with women living with HIV and clinicians working with women living with HIV to investigate motivations and barriers to gender-equitable representation in HIV clinical research. Participant motivations for participation included altruistic desires to benefit younger women, and to optimise resulting interventions. Women living with HIV expressed optimism that a cure would dispel HIV-related stigma and brings about substantial material improvement to their lives. Reluctance to participate related to concerns regarding potential side-effects, antiretroviral treatment interruption, and impacts on fertility. Unfamiliarity with trials, confidentiality concerns and logistical difficulties were also cited. Lastly, onerous eligibility criteria, clinicians' assumptions about women's willingness and ability to meaningfully provide consent to participation were cited as barriers which could be addressed. Bolstering women's participation in HIV cure research requires consideration of factors relating to reproductive health, analytical treatment interruption, and recruitment. Engaging women living with HIV in trial design and promotion may help overcome these issues

Family medicine · Sociology · Biomedical Ethics and Regulation · Ethics in Clinical Research · Gender Studies · Medicine · Psychology · Qualitative Research Methods and Ethics · Gerontology

  • From initial awareness to sustained involvement

    Open Access•Maaike A J Noorman, Kim Romijnders et al.•AIDS Care•2026

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    Jane Ritchie, Liz Spencer•Analyzing Qualitative Data•2010

  • The Joint United Nations Programme on HIV/Aids

    Benjamin Mason Meier, Helena Nygren-Krug et al.•Human Rights in Global Health•2018

  • Saturation

    Open Access•Malcolm Tight•Qualitative Inquiry•2024

  • HIV-Related Knowledge and Practices among Asian and African Migrants Living in Australia

    Open Access•Daniel Vujcich, Alison Reid et al.•International Journal of…•2023

  • The predictors of unsuppressed viremia among PLHIV

    Open Access•Lydia Boampong Owusu, Christiana Ababio et al.•BMC Public Health•2023

  • Children and Careers

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Obras citantes distintas1
Citas por año1
Intervalo de citas2026 - 2026 (1)
Velocidad de citacióncurrent
Altamente citadoNo
Tipos de citaNeutras: 1
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