Literature DB >> 1456273

Institutional Review Board (IRB) review lacks impact on the readability of consent forms for research.

D E Hammerschmidt1, M A Keane.   

Abstract

Consent forms in research are a source of current and retrospective information for the subject, a "prompt" for the person who is obtaining consent, and a documentation of the "informed" consent process and its adequacy. Occasionally, these forms may be administered by inexperienced trainees or ancillary personnel, and thus stand virtually alone. Therefore, the forms must be inherently comprehensible to the subjects. To test whether this is the case, 65 new applications were randomly selected from 13 consecutive IRB agendas, and their consent documents were computer-analyzed (Flesch/Fry scoring) after correction for expected confounding features, such as lists, tables, and polysyllabic proper names and jargon. Mean U.S. school grade for 70% comprehension (Fry score) was 15.03 +/- 0.19 (standard error of the mean), implying readability by 37.4 +/- 1% of the U.S. adult population. In contrast, a consecutive sampling of 21 Ann Landers columns yielded a mean Fry score of 7.67 +/- 0.5 (p < 0.01; readable by 75 +/- 3%). Fifteen Reader's Digest articles yielded a mean Fry score of 9.95 +/- 0.65 (p < 0.01; readable by 59.1 +/- 3%), and 15 "Talk of the Town" columns from The New Yorker averaged a grade level of 13.3 +/- 0.83; p < 0.01; readable by 42.7% +/- 4.8%). No document was improved by more than one grade level by the IRB review process, and most were unchanged.(ABSTRACT TRUNCATED AT 250 WORDS)

Entities:  

Keywords:  Biomedical and Behavioral Research; Empirical Approach; University of Minnesota

Mesh:

Year:  1992        PMID: 1456273     DOI: 10.1097/00000441-199212000-00003

Source DB:  PubMed          Journal:  Am J Med Sci        ISSN: 0002-9629            Impact factor:   2.378


  8 in total

Review 1.  Ethical issues in the development of new agents.

Authors:  C K Daugherty
Journal:  Invest New Drugs       Date:  1999       Impact factor: 3.850

2.  The use of multimedia in the informed consent process.

Authors:  H B Jimison; P P Sher; R Appleyard; Y LeVernois
Journal:  J Am Med Inform Assoc       Date:  1998 May-Jun       Impact factor: 4.497

3.  Can the written information to research subjects be improved?--an empirical study.

Authors:  E Bjørn; P Rossel; S Holm
Journal:  J Med Ethics       Date:  1999-06       Impact factor: 2.903

Review 4.  Easy-to-read informed consent forms for hematopoietic cell transplantation clinical trials.

Authors:  Ellen M Denzen; Martha E Burton Santibáñez; Heather Moore; Amy Foley; Iris D Gersten; Cathy Gurgol; Navneet S Majhail; Ryan Spellecy; Mary M Horowitz; Elizabeth A Murphy
Journal:  Biol Blood Marrow Transplant       Date:  2011-07-30       Impact factor: 5.742

Review 5.  Technical editing of research reports in biomedical journals.

Authors:  Elizabeth Wager; Philippa Middleton
Journal:  Cochrane Database Syst Rev       Date:  2008-10-08

6.  Comprehensibility of translated informed consent documents used in clinical research in psychiatry.

Authors:  Venu Gopal Jhanwar; Ram Jeevan Bishnoi
Journal:  Indian J Psychol Med       Date:  2010-01

7.  Readability and understandability of clinical research patient information leaflets and consent forms in Ireland and the UK: a retrospective quantitative analysis.

Authors:  Lydia O'Sullivan; Prasanth Sukumar; Rachel Crowley; Eilish McAuliffe; Peter Doran
Journal:  BMJ Open       Date:  2020-09-03       Impact factor: 2.692

8.  A novel metadata management model to capture consent for record linkage in longitudinal research studies.

Authors:  Christiana McMahon; Spiros Denaxas
Journal:  Inform Health Soc Care       Date:  2017-11-06       Impact factor: 2.439

  8 in total

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