E-Consent—a guide to maintain recruitment in clinical trials during the COVID-19 pandemic

BACKGROUND: The COVID-19 pandemic has posed daunting challenges when conducting clinical research. Adopting new technologies such as remote electronic consent (e-Consent) can help overcome them. However, guidelines for e-Consent implementation in ongoing clinical trials are currently lacking. The Ne...

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Detalles Bibliográficos
Autores principales: Almeida-Magana, Ricardo, Maroof, Hanna, Grierson, Jack, Clow, Rosie, Dinneen, Eoin, Al-Hammouri, Tarek, Muirhead, Nicola, Brew-Graves, Chris, Kelly, John, Shaw, Greg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Methodology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9096749/
https://www.ncbi.nlm.nih.gov/pubmed/35550639
http://dx.doi.org/10.1186/s13063-022-06333-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9096749/
https://www.ncbi.nlm.nih.gov/pubmed/35550639
http://dx.doi.org/10.1186/s13063-022-06333-6

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