Initial Steps in Creating a Patient-Centric Addendum to Clinical Trial Informed Consent Forms

INTRODUCTION: The purpose of the informed consent form (ICF) is to outline the risks and benefits of an interventional clinical trial to potential participants. The aim of this study was to explore the feasibility of a short addendum to the ICF, summarizing key points most relevant to potential part...

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Detalles Bibliográficos
Autores principales: King-Kallimanis, Bellinda L., Ferris, Andrea, Dropkin, Lisa, Molina, Mariel, Redway, Lydia, Gerber, David E., Grant, Tracey L., Roy, Upal Basu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Brief Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568273/
https://www.ncbi.nlm.nih.gov/pubmed/37842324
http://dx.doi.org/10.1016/j.jtocrr.2023.100575

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10568273/
https://www.ncbi.nlm.nih.gov/pubmed/37842324
http://dx.doi.org/10.1016/j.jtocrr.2023.100575

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