Implementing a New Common Rule Requirement for Informed Consent: A Randomized Trial on Adult Asthma Patients

Objectives. To determine how the format of a clinical trial informed consent document can affect participants’ retention of enrollment-relevant information. Background. Recent changes to the US Federal Common Rule require informed consent documents for clinical trials to be concise and start with th...

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Detalles Bibliográficos
Autores principales: Yu, Michael, Fischhoff, Baruch, Krishnamurti, Tamar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2019
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6440037/
https://www.ncbi.nlm.nih.gov/pubmed/30944885
http://dx.doi.org/10.1177/2381468319839315

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6440037/
https://www.ncbi.nlm.nih.gov/pubmed/30944885
http://dx.doi.org/10.1177/2381468319839315

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