了解临床试验中电子同意书的伦理。

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Trials Pub Date : 2024-08-16 DOI:10.1186/s13063-024-08330-3
Katherine Sahan, Rohan Wijesurendra, David Preiss, Marion Mafham, Mark Sheehan
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引用次数: 0

摘要

在随机试验中使用电子同意书(e-consent)有很好的现实理由,尤其是在进行大规模临床试验以回答人群层面的健康研究问题时。然而,确定电子同意的伦理理由并不那么明确,这取决于正确理解电子同意在临床试验中的含义及其伦理意义。在此,我们重点讨论具有伦理意义的四个特征,这些特征引发了与电子同意有关的一系列伦理问题,值得进一步开展有针对性的伦理研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Towards an understanding of the ethics of electronic consent in clinical trials.

There are good practical reasons to use electronic consent (e-consent) in randomised trials, especially when conducting large-scale clinical trials to answer population-level health research questions. However, determining ethical reasons for e-consent is not so clear and depends on a proper understanding of what e-consent means when used in clinical trials and its ethical significance. Here we focus on four features of ethical significance which give rise to a range of ethical considerations relating to e-consent and merit further focused ethics research.

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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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