Study protocol for a randomised controlled trial of enhanced informed consent compared to standard informed consent to improve patient understanding of early phase oncology clinical trials (CONSENT)

INTRODUCTION: Early phase cancer clinical trials have become increasingly complicated in terms of patient selection and trial procedures—this is reflected in the increasing length of participant information sheets (PIS). Informed consent for early phase clinical trials has been contentious due to th...

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Detalles Bibliográficos
Autores principales: Pal, Abhijit, Stapleton, Sarah, Yap, Christina, Lai-Kwon, Julia, Daly, Robert, Magkos, Dimitrios, Baikady, Bindumalini Rao, Minchom, Anna, Banerji, Udai, De Bono, Johann, Karikios, Deme, Boyle, Frances, Lopez, Juanita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Oncology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8422487/
https://www.ncbi.nlm.nih.gov/pubmed/34489282
http://dx.doi.org/10.1136/bmjopen-2021-049217

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8422487/
https://www.ncbi.nlm.nih.gov/pubmed/34489282
http://dx.doi.org/10.1136/bmjopen-2021-049217

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