Participation in Clinical Research Could Modify Background Risk for Trial Outcome Measures

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dc.contributor.authorAbaasa, Andrew M.
dc.contributor.authorAsiki, Gershim
dc.contributor.authorLevin, Jonathan
dc.contributor.authorBahemuka, Ubaldo
dc.contributor.authorRuzagira, Eugene
dc.contributor.authorKibengo, Freddie M.
dc.contributor.authorMulondo, Jerry
dc.contributor.authorNdibazza, Juliet
dc.contributor.authorPrice, Matthew A.
dc.contributor.authorFast, Pat
dc.contributor.authorKamali, Anatoli
dc.date.accessioned2022-01-30T14:47:13Z
dc.date.available2022-01-30T14:47:13Z
dc.date.issued2014
dc.description.abstractData on HIV incidence and retention are needed to inform study design of efficacy trials. However, the selection criteria and interventions during an actual clinical trial could reduce HIV incidence and thus affect the statistical power. We investigated the effect of inclusion and participation in a simulated vaccine efficacy trial (SiVET) on HIV and pregnancy incidence in a fisherfolk cohort in SW Uganda.en_US
dc.identifier.citationAbaasa, A. M., Asiki, G., Levin, J., Bahemuka, U., Ruzagira, E., Kibengo, F. M., ... & Kamali, A. (2014). Participation in Clinical Research Could Modify Background Risk for Trial Outcome Measures. AIDS Research and Human Retroviruses, 30(S1), A213-A214. https://doi.org/10.1089/aid.2014.5462.abstracten_US
dc.identifier.urihttps://doi.org/10.1089/aid.2014.5462.abstract
dc.identifier.urihttps://nru.uncst.go.ug/xmlui/handle/123456789/1624
dc.language.isoenen_US
dc.publisherAIDS Research and Human Retrovirusesen_US
dc.subjectClinical Researchen_US
dc.subjectRisken_US
dc.subjectTrial Outcome Measuresen_US
dc.titleParticipation in Clinical Research Could Modify Background Risk for Trial Outcome Measuresen_US
dc.typeArticleen_US
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