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Informed Consent and Placebo Effects: A Content Analysis of Information Leaflets to Identify What Clinical Trial Participants Are Told about Placebos

Overview of attention for article published in PLOS ONE, June 2012
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Title
Informed Consent and Placebo Effects: A Content Analysis of Information Leaflets to Identify What Clinical Trial Participants Are Told about Placebos
Published in
PLOS ONE, June 2012
DOI 10.1371/journal.pone.0039661
Pubmed ID
Authors

Felicity L. Bishop, Alison E. M. Adams, Ted J. Kaptchuk, George T. Lewith

Abstract

Placebo groups are used in randomised clinical trials (RCTs) to control for placebo effects, which can be large. Participants in trials can misunderstand written information particularly regarding technical aspects of trial design such as randomisation; the adequacy of written information about placebos has not been explored. We aimed to identify what participants in major RCTs in the UK are told about placebos and their effects.

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X Demographics

The data shown below were collected from the profiles of 15 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 61 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United Kingdom 2 3%
Germany 1 2%
Unknown 58 95%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 13 21%
Student > Ph. D. Student 9 15%
Student > Master 8 13%
Other 6 10%
Researcher 5 8%
Other 8 13%
Unknown 12 20%
Readers by discipline Count As %
Medicine and Dentistry 18 30%
Psychology 10 16%
Biochemistry, Genetics and Molecular Biology 5 8%
Philosophy 3 5%
Pharmacology, Toxicology and Pharmaceutical Science 3 5%
Other 10 16%
Unknown 12 20%