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Can user testing of a clinical trial patient information sheet make it fit-for-purpose? - a randomized controlled trial

机译:用户对临床试验患者信息表的测试能否使其适合目的? -随机对照试验

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摘要

BackgroundThe participant information sheet (PIS) provided to potential trial participants is a critical part of the process of valid consent. However, there is long-standing concern that these lengthy and complex documents are not fit-for-purpose. This has been supported recently through the application of a performance-based approach to testing and improving readability called user testing. This method is now widely used to improve patient medicine leaflets - determining whether people can find and understand key facts. This study applied for the first time a controlled design to determine whether a PIS developed through user testing had improved readability over the original, using a sheet from a UK trial in acute myeloid leukemia (AML16).
机译:背景信息提供给潜在试验参与者的参与者信息表(PIS)是有效同意过程的关键部分。但是,长期以来人们一直担心这些冗长而复杂的文档不适合使用。最近,通过使用一种基于性能的方法来测试和提高称为用户测试的可读性,对此提供了支持。现在,这种方法被广泛用于改善患者的医疗传单-确定人们是否可以找到并了解关键事实。这项研究使用英国急性髓样白血病(AML16)试验中的一张表,首次应用了受控设计来确定通过用户测试开发的PIS是否具有比原先更高的可读性。

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