Abstract
BackgroundBefore participation in medical research an informed consent must be obtained. This study investigates whether the readability of patient information and consent documents (PICDs) corresponds to the average educational level of participants in rheumatological studies in the Netherlands, Denmark, and Norway.Methods24 PICDs from studies were collected and readability was assessed independently using the Gunning’s Fog Index (FOG) and Simple Measure of Gobbledygook (SMOG) grading.ResultsThe mean score for the FOG and SMOG grades were 14.2 (9.0–19.0) and 14.2 (12–17) respectively. The mean FOG and SMOG grades were 12.7 and 13.3 in the Dutch studies, 15.0 and 14.9 in the Danish studies, and 14.6 and 14.3 in the Norwegian studies, respectively. Out of the 2865 participants, more than 57 % had a lower educational level than the highest readability score calculated in the individual study.ConclusionsAs the readability level of the PICDs did not match the participants’ educational level, consent may not have been valid, as the participants may have had a limited understanding of what they agreed to participate in. There should be more focus on the readability of PICDs. National guidelines for how to write clear and unambiguous PICDs in simple and easily understandable language could increase the focus on the readability of PICD.Electronic supplementary materialThe online version of this article (doi:10.1186/s12910-016-0126-0) contains supplementary material, which is available to authorized users.
Highlights
Before participation in medical research an informed consent must be obtained
This study examines the readability of written patient information and consent documents (PICDs) used in rheumatology research
This study aims to document whether the readability of PICDs corresponds with reported education or schooling level of the participants enrolled in rheumatological studies
Summary
Before participation in medical research an informed consent must be obtained. This study investigates whether the readability of patient information and consent documents (PICDs) corresponds to the average educational level of participants in rheumatological studies in the Netherlands, Denmark, and Norway. This study examines the readability of written patient information and consent documents (PICDs) used in rheumatology research. Ethical guidelines for medical research on human beings, which includes PICDs, were developed by the World Medical Association in Helsinki in 1964 [1]. The guidelines has been revised several times, the last time in 2013 [2]. The guidelines have been implemented by National Ethic Committees [3,4,5]
Published Version (Free)
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.