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

Abstract:
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.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1186/s13063-024-08330-3

Authors


More by this author
Institution:
University of Oxford
Department:
Big Data Institute
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Surgical Sciences
Sub department:
Clinical Trial Service Unit
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Surgical Sciences
Sub department:
Clinical Trial Service Unit
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Surgical Sciences
Sub department:
Clinical Trial Service Unit
Role:
Author
More by this author
Institution:
University of Oxford
Department:
Big Data Institute
Role:
Author
ORCID:
0000-0002-7191-901X


Publisher:
BioMed Central
Journal:
Trials More from this journal
Volume:
25
Issue:
1
Article number:
545
Publication date:
2024-08-16
Acceptance date:
2024-07-08
DOI:
EISSN:
1745-6215
ISSN:
1745-6215


Language:
English
Pubs id:
2022188
Local pid:
pubs:2022188
Source identifiers:
2195333
Deposit date:
2024-08-17
This ORA record was generated from metadata provided by an external service. It has not been edited by the ORA Team.

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