Adamson Joy, Cockayne Sarah, Puffer Suezann, Torgerson David J
York Trials Unit, Department of Health Sciences, University of York, York YO10 5DD, UK.
Contemp Clin Trials. 2006 Aug;27(4):305-19. doi: 10.1016/j.cct.2005.11.003. Epub 2006 Feb 7.
In 1979, Zelen described a trial method of randomising participants before acquiring consent in order to enhance recruitment to clinical trials. The method has been criticised ethically due to lack of consent and scientifically due to high crossover rates. This paper reviews recent published trials using this method and describes the reasons authors gave for using the method, examines the crossover rates, and looks at the quality of identified trials.
Literature review searching for all citations to the relevant Zelen's papers of trials published since 1990 plus inclusion of trials from personal knowledge.
We identified 58 relevant trials. The most common justification for the use of Zelen method was to avoid the introduction of bias (e.g., to avoid the Hawthorne effect). Few trialists had explicitly used the design to enhance participant recruitment. Most trials (n=41) experienced some crossover from one group to the other (median crossover=8.9%, mean=13.8%, IQR 2.6% to 15%) although this was usually within acceptable limits.
The most important reason stated by authors for using Zelen's method was to limit bias. Zelen's method, if carefully used, can avoid 'resentful demoralisation' and the Hawthorne effect biasing a trial. Unlike a previous review, we found that crossover was not a problem for most trials.
1979年,泽伦描述了一种在获得同意之前对参与者进行随机分组的试验方法,以提高临床试验的招募率。由于缺乏同意,该方法在伦理上受到批评;又因交叉率高,在科学上也受到批评。本文回顾了最近使用该方法的已发表试验,描述了作者使用该方法的原因,检查了交叉率,并审视了所确定试验的质量。
文献综述,检索自1990年以来发表的所有引用泽伦相关试验论文的文献,并纳入个人所知的试验。
我们确定了58项相关试验。使用泽伦方法最常见的理由是避免引入偏差(例如,避免霍桑效应)。很少有试验者明确使用该设计来提高参与者招募率。大多数试验(n = 41)经历了从一组到另一组的一些交叉(中位数交叉率 = 8.9%,平均值 = 13.8%,四分位间距2.6%至15%),尽管这通常在可接受范围内。
作者使用泽伦方法陈述的最重要原因是限制偏差。如果谨慎使用,泽伦方法可以避免“怨恨性士气低落”和霍桑效应使试验产生偏差。与之前的综述不同,我们发现交叉对大多数试验来说不是问题。