Literature DB >> 22537428

Informed consent documents do not encourage good-quality decision making.

Jamie C Brehaut1, Kelly Carroll, Glyn Elwyn, Raphael Saginur, Jonathan Kimmelman, Kaveh Shojania, Ania Syrowatka, Trang Nguyen, Erica Hoe, Dean Fergusson.   

Abstract

OBJECTIVE: Informed consent for research has emphasized information provision over support to people making a difficult decision. We assessed the extent to which existing informed consent documents (ICDs) conform to the International Patient Decision Aid Standards for supporting decision making. STUDY DESIGN AND
SETTING: One hundred thirty-nine ICDs for trials registered with ClinicalTrials.gov were obtained from study investigators. Using a four-point scale, two raters assessed each ICD on 32 items.
RESULTS: Overall agreement between raters was 95.1% (linear weighted kappa-0.745). For 12 items focused on providing enough information, conformity was above 50% for three, and 0% for another four. For all eight items focused on how to present outcome probabilities, conformity was below 20%. For two items focused on clarifying and expressing values, conformity was below 10%. For two items focused on improving structured guidance, conformity was below 5%. For four items focused on using evidence, one item showed conformity of 74%; all others showed conformity below 5%. For four items focused on transparency, conformity was high (above 60% for two, above 80% for the others).
CONCLUSIONS: Existing ICDs do not meet most validated standards for encouraging good decision making. These standards make clear predictions about how one might improve ICDs ensure that research participants are fully informed.
Copyright © 2012 Elsevier Inc. All rights reserved.

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Year:  2012        PMID: 22537428     DOI: 10.1016/j.jclinepi.2012.01.004

Source DB:  PubMed          Journal:  J Clin Epidemiol        ISSN: 0895-4356            Impact factor:   6.437


  16 in total

1.  Surrogate Informed Consent: A Qualitative Analysis of Surrogate Decision Makers' Perspectives.

Authors:  Trevor Lane; Elinor Brereton; Carolyn Nowels; Jeffrey McKeehan; Marc Moss; Daniel D Matlock
Journal:  Ann Am Thorac Soc       Date:  2021-07

2.  Did I Tell You That? Ethical Issues Related to Using Computational Methods to Discover Non-Disclosed Patient Characteristics.

Authors:  Kenrick D Cato; Walter Bockting; Elaine Larson
Journal:  J Empir Res Hum Res Ethics       Date:  2016-07       Impact factor: 1.742

3.  Consent for participating in clinical trials - Is it really informed?

Authors:  Teodora Alexa-Stratulat; Marius Neagu; Anca-Iulia Neagu; Ioana Dana Alexa; Beatrice Gabriela Ioan
Journal:  Dev World Bioeth       Date:  2018-06-22       Impact factor: 2.294

4.  Informed consent in clinical research: Consensus recommendations for reform identified by an expert interview panel.

Authors:  Beverly H Lorell; J Stephen Mikita; Annick Anderson; Zachary P Hallinan; Annemarie Forrest
Journal:  Clin Trials       Date:  2015-07-15       Impact factor: 2.486

5.  Protocol of a randomized controlled trial of an erythropoietin stimulating agent decision aid for anemia treatment in kidney disease.

Authors:  Lauren B Beach; Marcus Wild; Gowri Ramachandran; H Omer Ikizler; Kerri L Cavanaugh
Journal:  BMC Nephrol       Date:  2016-07-18       Impact factor: 2.388

6.  Exploring informed consent in HIV clinical trials: A case study in Uganda.

Authors:  Agnes Ssali; Fiona Poland; Janet Seeley
Journal:  Heliyon       Date:  2016-11-14

7.  Permission form synopses to improve parents' understanding of research: a randomized trial.

Authors:  C T D'Angio; H Wang; J E Hunn; G S Pryhuber; P R Chess; S Lakshminrusimha
Journal:  J Perinatol       Date:  2017-03-30       Impact factor: 2.521

Review 8.  Decision aids for people considering taking part in clinical trials.

Authors:  Katie Gillies; Seonaidh C Cotton; Jamie C Brehaut; Mary C Politi; Zoe Skea
Journal:  Cochrane Database Syst Rev       Date:  2015-11-27

9.  Practice variation across consent templates for biobank research. a survey of German biobanks.

Authors:  Irene Hirschberg; Hannes Knüppel; Daniel Strech
Journal:  Front Genet       Date:  2013-11-14       Impact factor: 4.599

10.  Patient information leaflets (PILs) for UK randomised controlled trials: a feasibility study exploring whether they contain information to support decision making about trial participation.

Authors:  Katie Gillies; Wan Huang; Zoë Skea; Jamie Brehaut; Seonaidh Cotton
Journal:  Trials       Date:  2014-02-18       Impact factor: 2.279

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