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Assessment of the understanding of informed consent including participants’ experiences, and generation of a supplemental consent decision aid for Gestational Diabetes Mellitus (GDM) research

Background: Informed consent is a basic ethical requirement of clinical research, yet deficiencies have been documented in the comprehension of its components among trial participants. Pregnancy research is sparsely conducted. Assessment of understanding of the informed consent among pregnant women...

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Detalles Bibliográficos
Autores principales: Atal, Shubham, Dunne, Fidelma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6973531/
https://www.ncbi.nlm.nih.gov/pubmed/32002505
http://dx.doi.org/10.12688/hrbopenres.12811.1

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