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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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Detalhes bibliográficos
Publicado no:HRB Open Res
Main Authors: Atal, Shubham, Dunne, Fidelma
Formato: Artigo
Idioma:Inglês
Publicado em: F1000 Research Limited 2018
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6973531/
https://ncbi.nlm.nih.gov/pubmed/32002505
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.12688/hrbopenres.12811.1
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