Raymond Elizabeth G, Chen Pai Lien, Pierre-Louis Bosny, Luoto Joanne, Barnhart Kurt T, Bradley Lynn, Creinin Mitchell D, Poindexter Alfred, Wan Livia, Martens Mark, Schenken Robert, Nicholas Cate F, Blackwell Richard
Family Health International, Research Triangle Park, NC, USA.
BMC Med Res Methodol. 2004 Oct 1;4:23. doi: 10.1186/1471-2288-4-23.
In most recent large efficacy trials of barrier contraceptive methods, a high proportion of participants withdrew before the intended end of follow-up. The objective of this analysis was to explore characteristics of participants who failed to complete seven months of planned participation in a trial of spermicide efficacy.
Trial participants were expected to use the assigned spermicide for contraception for 7 months or until pregnancy occurred. In bivariable and multivariable analyses, we assessed the associations between failure to complete the trial and 17 pre-specified baseline characteristics. In addition, among women who participated for at least 6 weeks, we evaluated the relationships between failure to complete, various features of their first 6 weeks of experience with the spermicide, and characteristics of the study centers and population.
Of the 1514 participants in this analysis, 635 (42%) failed to complete the study for reasons other than pregnancy. Women were significantly less likely to complete if they were younger or unmarried, had intercourse at least 8 times per month, or were enrolled at a university center or at a center that enrolled fewer than 4 participants per month. Noncompliance with study procedures in the first 6 weeks was also associated with subsequent early withdrawal, but dissatisfaction with the spermicide was not. However, many participants without these risk factors withdrew early.
Failure to complete is a major problem in barrier method trials that seriously compromises the interpretation of results. Targeting retention efforts at women at high risk for early withdrawal is not likely to address the problem sufficiently.
在最近大多数屏障避孕方法的大型疗效试验中,很大一部分参与者在预定随访期结束前退出。本分析的目的是探讨在一项杀精剂疗效试验中未能完成七个月计划参与期的参与者的特征。
试验参与者预期使用分配的杀精剂避孕7个月或直至怀孕。在双变量和多变量分析中,我们评估了未完成试验与17个预先指定的基线特征之间的关联。此外,在参与至少6周的女性中,我们评估了未完成试验、她们使用杀精剂的前6周的各种特征、研究中心和人群特征之间的关系。
在本次分析的1514名参与者中,635名(42%)因非怀孕原因未能完成研究。如果女性年龄较小或未婚、每月至少性交8次、或在大学中心或每月招募少于4名参与者的中心登记,她们完成研究的可能性显著降低。前6周不遵守研究程序也与随后提前退出有关,但对杀精剂不满意则无关。然而,许多没有这些风险因素的参与者也提前退出了。
未完成是屏障方法试验中的一个主要问题,严重影响了结果的解释。将保留工作目标对准提前退出风险高的女性不太可能充分解决该问题。