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 the...

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Egile Nagusiak:	Christina Yap, Deme Karikios, Johann De Bono, Anna Minchom, Udai Banerji, Juanita Lopez, Sarah Stapleton, Frances Boyle, Abhijit Pal, Julia Lai-Kwon, Robert Daly, Dimitrios Magkos, Bindumalini Rao Baikady
Formatua:	Artigo
Hizkuntza:	Inglês
Argitaratua:	BMJ Publishing Group 2021-09-01
Saila:	BMJ Open
Sarrera elektronikoa:	https://bmjopen.bmj.com/content/11/9/e049217.full
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