TY - JOUR
T1 - The HVTN503/Phambili HIV vaccine trial
T2 - A comparison of younger and older participants
AU - Volk, Jonathan E.
AU - Hessol, Nancy A.
AU - Gray, Glenda E.
AU - Kublin, James G.
AU - Churchyard, Gavin J.
AU - Mlisana, Koleka
AU - Nchabeleng, Maphoshane
AU - Buchbinder, Susan P.
AU - Bekker, Linda Gail
PY - 2014/4
Y1 - 2014/4
N2 - By comparing younger to older participants enrolled in a HIV vaccine efficacy trial, we aimed to gain insights into the inclusion of adolescents in future trials. This was a sub-analysis of a multisite HIV vaccine randomized clinical trial in South Africa, conducted January-September 2007. Motivations for trial enrolment, social harms, adverse events and loss to follow-up were compared between younger (18-20 years old) and older participants (21-35 years old). Both younger (n = 238) and older participants (n = 563) were equally likely to report enrolling for altruistic reasons. Younger females were less likely than older participants to join for trial reimbursement (p = 0.005), while younger males were more likely to enrol because the vaccine may provide protection from HIV-acquisition (p < 0.001). There were no significant differences in the number of social harms reported. Compared to males over 20 years old, 18-20-year-old females were less likely to experience adverse events (OR = 0.1, CI 0.01-0.80) and no more likely to be lost to follow-up (OR = 0.7, CI 0.39-1.25), while 18-20-year-old males were no more likely to experience adverse events (OR = 1.3, CI 0.58-2.83) or loss to follow-up (OR = 0.8, CI 0.51-1.41). Our data support the inclusion of younger participants who are at risk for HIV in future HIV vaccine efficacy trials.
AB - By comparing younger to older participants enrolled in a HIV vaccine efficacy trial, we aimed to gain insights into the inclusion of adolescents in future trials. This was a sub-analysis of a multisite HIV vaccine randomized clinical trial in South Africa, conducted January-September 2007. Motivations for trial enrolment, social harms, adverse events and loss to follow-up were compared between younger (18-20 years old) and older participants (21-35 years old). Both younger (n = 238) and older participants (n = 563) were equally likely to report enrolling for altruistic reasons. Younger females were less likely than older participants to join for trial reimbursement (p = 0.005), while younger males were more likely to enrol because the vaccine may provide protection from HIV-acquisition (p < 0.001). There were no significant differences in the number of social harms reported. Compared to males over 20 years old, 18-20-year-old females were less likely to experience adverse events (OR = 0.1, CI 0.01-0.80) and no more likely to be lost to follow-up (OR = 0.7, CI 0.39-1.25), while 18-20-year-old males were no more likely to experience adverse events (OR = 1.3, CI 0.58-2.83) or loss to follow-up (OR = 0.8, CI 0.51-1.41). Our data support the inclusion of younger participants who are at risk for HIV in future HIV vaccine efficacy trials.
KW - AIDS
KW - HIV
KW - South Africa
KW - clinical trials
KW - prevention
KW - vaccination
KW - vaccine trials
KW - youth
UR - http://www.scopus.com/inward/record.url?scp=84898686977&partnerID=8YFLogxK
U2 - 10.1177/0956462413506892
DO - 10.1177/0956462413506892
M3 - Article
C2 - 24104693
AN - SCOPUS:84898686977
SN - 0956-4624
VL - 25
SP - 332
EP - 340
JO - International Journal of STD and AIDS
JF - International Journal of STD and AIDS
IS - 5
ER -