Publication:
Expectation of volunteers towards the vaccine efficacy of the prime-boost HIV vaccine phase III trial during unblinding

dc.contributor.authorKessuda Khowsroyen_US
dc.contributor.authorJittima Dhitavaten_US
dc.contributor.authorYupa Sabmeeen_US
dc.contributor.authorPataramon Laowarakulen_US
dc.contributor.authorJutarat Wattanakitwichaien_US
dc.contributor.authorJiraporn Auetianen_US
dc.contributor.authorKannika Lothongen_US
dc.contributor.authorRoongtip Boondaoen_US
dc.contributor.authorSarawan Maythaarttaphongen_US
dc.contributor.authorSunee Yaemwongen_US
dc.contributor.authorJean Louis Excleren_US
dc.contributor.authorSupachai Rerks-Ngarmen_US
dc.contributor.authorPunnee Pitisuttithumen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherUS Military HIV Research Programen_US
dc.contributor.otherThailand Ministry of Public Healthen_US
dc.date.accessioned2018-11-09T02:24:58Z
dc.date.available2018-11-09T02:24:58Z
dc.date.issued2014-01-01en_US
dc.description.abstract© 2014 Mary Ann Liebert, Inc. A Phase III community-based HIV vaccine trial using the ALVAC-HIV and AIDSVAX B/E prime-boost regimen (RV144) showed a modest vaccine efficacy of 31.2% against HIV acquisition. Participant's understanding of the trial is a key element of its success. This study aimed to understand participant's expectation and response to the overall results of the trial as well after unblinding. Using an open-ended questionnaire, data were collected from 400 participants who came for the unblinding visit. Fifty-three percent received the vaccine and 47% were placebo recipients. The median age was 30 years (range: 22-37). The observed vaccine efficacy of 31.2% was lower than expected by 67.75% of participants compared to higher than expected (by 6%), as expected (by 11.25%), and those with no expectation (15%). A majority of participants (71.5%) were happy and proud, and indicated that it was a good result. The rest were sad or disappointed (22.75%) or acquiescent (5.75%). After unblinding, 67.92% of the vaccine recipients had a positive response and 32.08% were acquiescent. Among placebo recipients, 85.11% were acquiescent and 10.11% indicated that being assigned to the vaccine group would have been better even though vaccine efficacy was only 31.2%. Despite the modest vaccine efficacy, a majority of study participants acknowledged the value of the trial and hoped that information from RV144 could be used for future vaccine development.en_US
dc.identifier.citationAIDS Research and Human Retroviruses. Vol.30, No.11 (2014), 1041-1045en_US
dc.identifier.doi10.1089/aid.2013.0136en_US
dc.identifier.issn19318405en_US
dc.identifier.issn08892229en_US
dc.identifier.other2-s2.0-84931351656en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/34055
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84931351656&origin=inwarden_US
dc.subjectImmunology and Microbiologyen_US
dc.subjectMedicineen_US
dc.titleExpectation of volunteers towards the vaccine efficacy of the prime-boost HIV vaccine phase III trial during unblindingen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84931351656&origin=inwarden_US

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