People living with HIV

Abdool Karim, Q., Abdool Karim, S. S., Coovadia, H. M., & Susser, M. (1998). Informed consent for HIV testing in a South
African hospital: Is it truly informed and truly voluntary?
. American Journal of Public Health, 88(4), 637-640.
Informed consent (adults), Voluntariness and self-efficacy, Adults (other), People living with HIV, People at risk for or with other STIs, Survey research, Health-care facilities, South AfricaQuantitative (QT)

Agnarson, A. M., et al. (2013). Antiretroviral Treatment Knowledge and Stigma – Implications for Programs and HIV Treatment Interventions in Rural Tanzanian Populations. PLoS ONE 8(1): e53993.
Informed consent (adults), Stigma, Adults (other), People at risk for HIV, People at risk for or with other STIs, People living with HIV, Survey research, Community-engaged researchCommunity organizations, TanzaniaQuantitative (QT)

Barnett, P. G., Hall, S. M., Haug, N. A., Sorensen, J. L., & Wong, W. (2008). Effect of incentives for medication adherence on health care use and costs in methadone patients with HIV. Drug Alcohol Dependence, 1, 115-121.                                                         Research risks and benefitsPeople living with HIVPeople who inject drugsClinical trialsHealth-care facilitiesUnited StatesQuantitative (QT)

Chenneville, T., Lynn, V., Peacock, B., Turner, D., & Marhefka, S. L. (2015). Disclosure of HIV status among female youth with HIV. Ethics and Behavior, 25 (4), 314-331.
StigmaAdolescentsPeople living with HIV, Health-care facilitiesSurvey researchUnited States, Qualitative (QL)

Franrenet, S., Moutel, G., Raffi, F., Dabis, F., Bruyand, M., Hervé, C., & … Duchange, N. (2011). Information that should be given to HIV cohort participants during ongoing research: The viewpoints of patient representatives and research professionals. Journal Of Empirical Research On Human Research Ethics, 6(4), 76-83.
Investigator practices and perspectives, Adults (other)People at risk for or living with other STIs, People living with HIV, Clinical trials, Health-care facilities, France, Mixed methods (MM)

Garber, M., Hanusa, B. H., Switzer, G. E., Mellors, J., & Arnold, R. M. (2007). HIV-infected African Americans are willing to participate in HIV treatment trials. Journal of General Internal Medicine, 22(1), 17-42.
Multicultural competence, Voluntariness and self-efficacy, People living with HIV, Clinical trials, Health-care facilities, United States, Quantitative (QT)

Lazovski, J., Losso, M., Krohmal, B., Emanuel, E. Z., Grady, C., & Wendler, D. (2009). Benefits and burdens of participation in a longitudinal clinical trial. Journal of Empirical Research on Human Research Ethics, 4(3), 89-97.
Research risks and benefits, People living with HIV, Clinical trials, Health-care facilities, Argentina, Brazil, Thailand, Quantitative (QT)

Madhivanan, P., Krupp, K., Kulkarni, V., Kulkarni, S., Vaidya, N., Shaheen, R. Philpott, S. & Fisher, C. B. (2014). HIV testing among pregnant women living with HIV in India: are private healthcare providers routinely violating women’s human rights? BMC International Health and Human Rights, 14(7).
Confidentiality and privacy, Informed consent (adults), People living with HIV, Clinical trials, Community organizations, Health-care facilities, India, Qualitative (QL)

Rajabiun, S., Mallinson, R. K., McCoy, K., Coleman, S., Drainoni, M., Rebholz, C., & Holbert, T. (2007). Getting me back on track: The role of outreach interventions in engaging and retaining people living with HIV/AIDS in medical care. AIDS Patient Care and STDs, 21(Supp. 1), S20-S29.
Clinical efficacy, Voluntariness and self-efficacy, People living with HIV, Health-care facilities, United States, Qualitative (QL)

Rautenbach, C., Lindegger, G., Slack, C., Wallace, M., & Newman, P. (2015). I’m positive, but I’m negative: competing voices in informed consent and implications for HIV vaccine trials. Journal of Empirical Research on Human Research Ethics, 10 (2), 151-156.
Informed consent (adults)People living with HIVClinical trialsHealth-care facilitiesSouth AfricaQualitative (QL)

Rongkavilit, C., Naar-King, S., Chuenyam, T., Wang, B., Wright, K., & Phanuphak, P. (2007). Health risk behaviors among HIV-infected youth in Bangkok, Thailand. Journal of Adolescent Health, 40, 358e1-358e8.
Assent and self-consent (children and adolescents), Adolescents, People living with HIV, Health-care facilities, Thailand, Quantitative (QT)

Teti, M., Murray, C., Johnson, L., & Binson, D. (2012). Photovoice as a community-based participatory research method among women living with HIV/AIDS: ethical opportunities and challenges. Journal Of Empirical Research On Human Research Ethics: JERHRE, 7(4), 34-43.
Confidentiality and privacy, People living with HIV, Community-engaged researchCommunity organization, United States, Qualitative (QL)

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