Literature DB >> 12594317

Readability standards for informed-consent forms as compared with actual readability.

Michael K Paasche-Orlow1, Holly A Taylor, Frederick L Brancati.   

Abstract

BACKGROUND: Institutional review boards (IRBs) are charged with safeguarding potential research subjects with limited literacy but may have an inadvertent role in promulgating unreadable consent forms. We hypothesized that text provided by IRBs in informed-consent forms falls short of the IRBs' own readability standards and that readability is influenced by the level of research activity, local literacy rates, and federal oversight.
METHODS: To test these hypotheses, we conducted a cross-sectional study linking data from several public-use sources. A total of 114 Web sites of U.S. medical schools were surveyed for IRB readability standards and informed-consent-form templates. Actual readability was measured with the Flesch-Kincaid scale, which assigns a score on the basis of the minimal grade level required to read and understand English text (range, 0 to 12). Data on the level of research activity, local literacy rates, and federal oversight were obtained from organizational Web sites.
RESULTS: The average readability score for text provided by IRBs was 10.6 (95 percent confidence interval, 10.3 to 10.8) on the Flesch-Kincaid scale. Specific readability standards, found on 61 Web sites (54 percent), ranged from a 5th-grade reading level to a 10th-grade reading level. The mean Flesch-Kincaid scores for the readability of sample text provided by IRBs exceeded the stated standard by 2.8 grade levels (95 percent confidence interval, 2.4 to 3.2; P<0.001). Readability was not associated with either the level of research funding (P=0.89) or local rates of literacy (P=0.92). However, the 52 schools that had been made subject to oversight by the Office for Human Research Protections (46 percent) had lower Flesch-Kincaid scores than the other schools (10.2 vs. 10.9, P=0.005).
CONCLUSIONS: IRBs commonly provide text for informed-consent forms that falls short of their own readability standards. Federal oversight is associated with better readability. Copyright 2003 Massachusetts Medical Society

Entities:  

Keywords:  Biomedical and Behavioral Research; Empirical Approach

Mesh:

Year:  2003        PMID: 12594317     DOI: 10.1056/NEJMsa021212

Source DB:  PubMed          Journal:  N Engl J Med        ISSN: 0028-4793            Impact factor:   91.245


  177 in total

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2.  To consent or not to consent, that is (not) the (sole) question. "And there is nothing new under the sun". Kohelet (also known as Ecclesiastes), 1:9. Bible.

Authors:  Didier Dreyfuss
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3.  A new look at informed consent for cancer clinical trials.

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Journal:  J Oncol Pract       Date:  2011-07       Impact factor: 3.840

Review 4.  Improving the informed consent process for research subjects with low literacy: a systematic review.

Authors:  Leonardo Tamariz; Ana Palacio; Mauricio Robert; Erin N Marcus
Journal:  J Gen Intern Med       Date:  2012-07-11       Impact factor: 5.128

5.  Assessing the readability of ClinicalTrials.gov.

Authors:  Danny T Y Wu; David A Hanauer; Qiaozhu Mei; Patricia M Clark; Lawrence C An; Joshua Proulx; Qing T Zeng; V G Vinod Vydiswaran; Kevyn Collins-Thompson; Kai Zheng
Journal:  J Am Med Inform Assoc       Date:  2015-08-11       Impact factor: 4.497

6.  "Entering a Clinical Trial: Is it Right for You?": a randomized study of The Clinical Trials Video and its impact on the informed consent process.

Authors:  Brianna Hoffner; Susan Bauer-Wu; Suzanne Hitchcock-Bryan; Mark Powell; Andrew Wolanski; Steven Joffe
Journal:  Cancer       Date:  2011-08-25       Impact factor: 6.860

7.  Improving informed consent with minority participants: results from researcher and community surveys.

Authors:  Sandra Crouse Quinn; Mary A Garza; James Butler; Craig S Fryer; Erica T Casper; Stephen B Thomas; David Barnard; Kevin H Kim
Journal:  J Empir Res Hum Res Ethics       Date:  2012-12       Impact factor: 1.742

8.  Protecting and respecting the vulnerable: existing regulations or further protections?

Authors:  Stephanie R Solomon
Journal:  Theor Med Bioeth       Date:  2013-02

9.  Using animation as an information tool to advance health research literacy among minority participants.

Authors:  Sheba George; Erin Moran; Nelida Duran; Robert A Jenders
Journal:  AMIA Annu Symp Proc       Date:  2013-11-16

10.  Using computer agents to explain medical documents to patients with low health literacy.

Authors:  Timothy W Bickmore; Laura M Pfeifer; Michael K Paasche-Orlow
Journal:  Patient Educ Couns       Date:  2009-03-17
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