Do informed consent documents for cancer trials do what they should? A study of manifest and latent functions

Though patient information leaflets (PILs) are provided to those invited to take part in medical research, they usually fall short in facilitating informed decisions about participation. We aimed to explore why there is an enduring requirement for a process that seems not to ‘work’, and to explain w...

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Bibliographic Details
Published in:	Sociology of health & illness Vol. 34; no. 8; pp. 1230 - 1245
Main Authors:	Armstrong, Natalie, Dixon‐Woods, Mary, Thomas, Anne, Rusk, Gill, Tarrant, Carolyn
Format:	Journal Article
Language:	English
Published:	Oxford, UK Blackwell Publishing Ltd 01-11-2012 Blackwell
Subjects:	Accountability Cancer Clinical trials Clinical Trials as Topic - standards communication Decision making Decisions Documents Ethics Ethics Committees, Research Female Health education Human Experimentation - standards Humans Informed Consent Informed Consent - ethics Male manifest and latent functions Medical Decision Making Medical ethics Medical Oncology Medical Research Participation Patients Social research Sociology Sociology of health and medicine Trials Values Participation trials documents Patient Document communication manifest and latent functions Cancer Medical Research
Online Access:	Get full text
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