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首页> 外文期刊>European journal of cancer care >Quality of online information about phase I clinical cancer trials in Sweden, Denmark and Norway
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Quality of online information about phase I clinical cancer trials in Sweden, Denmark and Norway

机译:关于丹麦,丹麦和挪威的关于I阶段临床癌症试验的在线信息的质量

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Abstract Patients increasingly search for online information about clinical trials. Little is known about the quality and readability of the information in these databases. Therefore, the aim of this study was to assess the quality and readability of online information available to the public on phase I clinical cancer trials in Sweden, Denmark and Norway. A qualitative content analysis was made of 19 online trial descriptions from three public websites in Sweden, Denmark and Norway, and the readability of the documents was tested. Both the quality of the content and the readability scores were best for the Danish information. The Swedish texts were very short and were the least readable. Overall, the quality of the information was highly variable and nearly all the documents were misleading in part. Furthermore, the descriptions provided almost no information about possible adverse effects or disadvantages of study participation. This study highlights a communication problem and proposes new ways of presenting studies that are less suggestive of positive outcomes, arguing that we should be more careful to include information about adverse effects, and that the use of simple measures like readability testing can be useful as an indicator of text quality.
机译:摘要患者越来越多地搜索有关临床试验的在线信息。对这些数据库中信息的质量和可读性知之甚少。因此,本研究的目的是评估公众在瑞典,丹麦和挪威的I阶段临床癌症试验中可用的在线信息的质量和可读性。定性内容分析由瑞典,丹麦和挪威的三个公共网站的19个在线试验说明制成,并测试了文件的可读性。内容的质量和可读性分数都是丹麦信息最适合的。瑞典文本非常短,是最不可读的。总体而言,信息的质量是高度变化的,几乎所有文件都在误导。此外,提供的描述几乎没有关于研究参与可能的不利影响或缺点的信息。本研究突出了沟通问题,提出了新的展示研究的展示性,这些研究较小的暗示性结果,争论我们应该更加谨慎地包括有关不利影响的信息,并且使用简单的措施如可读性测试的使用可以用作文本质量指标。

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