Towards an understanding of the ethics of electronic consent in clinical trials

被引：0
|
作者：
Sahan, Katherine [2 ]
Wijesurendra, Rohan [1 ]
Preiss, David [1 ]
Mafham, Marion [1 ]
Sheehan, Mark [2 ]
机构：
[1] Univ Oxford, Clin Trial Serv Unit, Oxford Populat Hlth, Richard Doll Bldg,Old Rd Campus,Roosevelt Dr, Oxford OX3 7LF, England
[2] Univ Oxford, Big Data Inst, Ethox Ctr, Oxford Populat Hlth, Old Rd Campus,Roosevelt Dr, Oxford OX3 7LF, England
来源：
TRIALS | 2024年 / 25卷 / 01期
关键词：
INFORMED-CONSENT; DESIGN;
D O I：
10.1186/s13063-024-08330-3
中图分类号：
R-3 [医学研究方法]; R3 [基础医学];
学科分类号：
1001 ;
摘要：
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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页数：7
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