Assessment of Length and Readability of Informed Consent Documents for COVID-19 Vaccine Trials

IMPORTANCE: Informed consent is a fundamental element of research ethics. The COVID-19 vaccine trials are high profile trials that have enrolled more than 100 000 participants. Consent documents must be succinct and understandable to ensure informed voluntary participation. OBJECTIVE: To assess how...

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Detalles Bibliográficos
Autores principales: Emanuel, Ezekiel J., Boyle, Connor W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Medical Association 2021
Materias:
Original Investigation
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8082317/
https://www.ncbi.nlm.nih.gov/pubmed/33909052
http://dx.doi.org/10.1001/jamanetworkopen.2021.10843

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8082317/
https://www.ncbi.nlm.nih.gov/pubmed/33909052
http://dx.doi.org/10.1001/jamanetworkopen.2021.10843

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