Exploring the experiences of substitute decision-makers with an exception to consent in a paediatric resuscitation randomised controlled trial: study protocol for a qualitative research study

INTRODUCTION: Prospective informed consent is required for most research involving human participants; however, this is impracticable under some circumstances. The Tri-Council Policy Statement: Ethical Conduct for Research Involving Humans (TCPS) outlines the requirements for research involving huma...

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Detalles Bibliográficos
Autores principales: Parker, Melissa J, de Laat, Sonya, Schwartz, Lisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2016
Materias:
Ethics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030536/
https://www.ncbi.nlm.nih.gov/pubmed/27625066
http://dx.doi.org/10.1136/bmjopen-2016-012931

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030536/
https://www.ncbi.nlm.nih.gov/pubmed/27625066
http://dx.doi.org/10.1136/bmjopen-2016-012931

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