Designing e-consent protocols for pragmatic clinical trials: case studies from a UKCRC clinical trials unit

Abstract Background Interest in and use of electronic consent (e-consent) in the conduct of academic clinical trials has increased since the COVID-19 pandemic. E-consent offers advantages including increased efficiency and accessibility, and reduced burden on site staff, which can be appealing to ac...

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Autori principali:	M. Hammond, P. Ashford, J. High, L. V. Clark, G. Howard, M. Jones, S. Stirling, C. West, on behalf of the Norwich CTU Methodology Group
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	BMC 2024-08-01
Serie:	Trials
Soggetti:	Informed consent E-consent Decentralised clinical trials Clinical trials
Accesso online:	https://doi.org/10.1186/s13063-024-08386-1
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