Abstract
To pilot the adherence readiness program, 60 patients planning to start HIV antiretrovirals were assigned to usual care (n = 31) or the intervention (n = 29), of whom 54 started antiretrovirals and were followed for up to 24 weeks. At week 24, the intervention had a large effect (50.0 % vs. 16.7 %, d = 0.75) on optimal dose-timing (85+ % doses taken on time) and small effect (54.2 % vs. 43.3 %, d = 0.22) on optimal dose-taking (85+ % doses taken) electronically monitored adherence, and medium effect on undetectable viral load (62 % 0.5 % vs. 43.4 %, d = 0.41), compared to usual care. These intervention benefits on adherence and viral suppression warrant further investigation.
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The research was supported by Grant R34MH085534 from the National Institute of Mental Health. The content of this paper does not necessarily represent the official views of the National Institute of Mental Health or the National Institutes of Health.
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Wagner, G.J., Lovely, P. & Schneider, S. Pilot Controlled Trial of the Adherence Readiness Program: An Intervention to Assess and Sustain HIV Antiretroviral Adherence Readiness. AIDS Behav 17, 3059–3065 (2013). https://doi.org/10.1007/s10461-013-0550-9
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DOI: https://doi.org/10.1007/s10461-013-0550-9