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.

引用

页数：7

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