Literature DB >> 1360426

Evaluating the readability of informed consent forms used in contraceptive clinical trials.

R Rivera1, J S Reed, D Menius.   

Abstract

The readability level of informed consent forms used in clinical trials on contraceptives was determined. Three different formulas for measuring readability were used. Some forms received relatively high scores by all three methods. The most common problems associated with high readability scores were the use of 'unfamiliar' words, long words and long sentences. At present all forms used must be readable, using the SMOG formula, at a grade 6 level or less.

Keywords:  Biomedical and Behavioral Research; Family Health International; Genetics and Reproduction

Mesh:

Year:  1992        PMID: 1360426     DOI: 10.1016/0020-7292(82)90133-3

Source DB:  PubMed          Journal:  Int J Gynaecol Obstet        ISSN: 0020-7292            Impact factor:   3.561


  3 in total

1.  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

2.  Informing patients about clinical trials.

Authors:  B J Oddens; A Algra; J van Gijn
Journal:  Clin Investig       Date:  1993-07

3.  A pilot study of simple interventions to improve informed consent in clinical research: feasibility, approach, and results.

Authors:  Nancy E Kass; Holly A Taylor; Joseph Ali; Kristina Hallez; Lelia Chaisson
Journal:  Clin Trials       Date:  2014-12-04       Impact factor: 2.486

  3 in total

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