Frew Paula, Parker Kimberly, Horton Takeia, Hixson Brooke, Flowers Lisa, Priddy Frances, Grohskopf Lisa, Mauck Christine, Workowski Kimberly
Emory University School of Medicine, Department of Medicine, Division of Infectious Diseases, USA ; Emory Center for AIDS Research, USA ; The Hope Clinic of the Emory Vaccine Center, USA ; Emory University, Rollins School of Public Health, USA.
Texas Woman's University, USA.
J AIDS Clin Res. 2012 Jul 3;Suppl 4(4). doi: 10.4172/2155-6113.S4-004.
This mixed methods study reports on product acceptance from a Phase I clinical trial of a candidate non-nucleoside reverse transcriptase inhibitor (NNRTI) vaginal microbicide product (UC781). The product was evaluated in the context of a Phase I clinical trial in an area characterized by high HIV prevalence among minority women. The findings will inform the development of an acceptable microbicide that will address the needs of diverse women and their partners.
This is a mixed methods study of 34 racially and ethnically diverse female participants and 10 male partners in Atlanta, Georgia. Chi-square tests for marginal homogeneity and kappa statistics were calculated to analyze differences between groups on product attributes and use intention. ANOVA was used to examine difference between the treatment groups. Qualitative data were analyzed via constant comparative methodology.
Thirty-four out of the original female cohort of 36 completed the questionnaire. Approval of future microbicide development was high at 91.2% (n=31) despite a lack of enthusiasm for the placebo and UC781 formulations. Overall female acceptability was correlated with personal protection motivation (r=1.00, p<0.001). African American women indicated greater likelihood of post-licensure microbicide use (X=7.9, p=0.048) and ascribed greater importance to its potential protection against HIV (X=18.7, p=0.001) and its potential for dual protection (protective against STIs and/or pregnancy) compared to white women (X=11.3, p=0.024). Men and women supported development in the form of an intravaginal ring or suppository. Men were more likely to encourage female adoption of the method if it afforded HIV protection (r=0.935, p=0.001).
Although most women agreed that the development of a microbicide was an important endeavor, quantitative and qualitative data indicated they would not use placebo or UC781 due to the objectionable viscosity, odor, and color. Male partners felt the potential protective benefit of a future microbicide product was its most important feature.
这项混合方法研究报告了一种候选非核苷类逆转录酶抑制剂(NNRTI)阴道杀菌剂产品(UC781)一期临床试验中的产品接受情况。该产品在一个少数族裔女性中艾滋病毒感染率较高的地区进行的一期临床试验中进行了评估。研究结果将为开发一种可接受的杀菌剂提供参考,以满足不同女性及其伴侣的需求。
这是一项针对佐治亚州亚特兰大市34名种族和族裔各异的女性参与者以及10名男性伴侣的混合方法研究。计算卡方边际同质性检验和kappa统计量,以分析各组在产品属性和使用意愿上的差异。方差分析用于检验治疗组之间的差异。定性数据通过持续比较法进行分析。
最初36名女性队列中有34名完成了问卷调查。尽管对安慰剂和UC781配方缺乏热情,但对未来杀菌剂开发的认可度高达91.2%(n = 31)。总体女性可接受性与个人保护动机相关(r = 1.00,p < 0.001)。与白人女性相比(X = 11.3,p = 0.024),非裔美国女性表示获得许可后使用杀菌剂的可能性更大(X = 7.9,p = 0.048),并且认为其对预防艾滋病毒的潜在保护作用(X = 18.7,p = 0.001)以及双重保护(预防性传播感染和/或怀孕)的潜力更为重要。男性和女性都支持以阴道环或栓剂的形式进行开发。如果该方法能提供艾滋病毒保护,男性更有可能鼓励女性采用(r = 0.935,p = 0.001)。
尽管大多数女性认为开发杀菌剂是一项重要的努力,但定量和定性数据表明,由于其令人反感的粘度、气味和颜色,她们不会使用安慰剂或UC781。男性伴侣认为未来杀菌剂产品的潜在保护益处是其最重要的特征。