The readability of information and consent forms in clinical research in France.
<h4>Background</h4>Quantitative tools have been developed to evaluate the readability of written documents and have been used in several studies to evaluate information and consent forms. These studies all showed that such documents had a low level of readability. Our objective is to eva...
Main Authors: | Véronique Ménoni, Noël Lucas, Jean François Leforestier, Jérôme Dimet, François Doz, Gilles Chatellier, Jean-Marc Tréluyer, Hélène Chappuy |
---|---|
Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2010-05-01
|
Series: | PLoS ONE |
Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/20485505/?tool=EBI |
Similar Items
-
Readability of the written study information in pediatric research in France.
by: Véronique Ménoni, et al.
Published: (2011-04-01) -
Examining the readability of patient-informed consent forms
by: Marli Terblanche, et al.
Published: (2010-10-01) -
Readability and Comprehensibility of Informed Consent Forms for Clinical Trials
by: Shu-Yu Chen, et al.
Published: (2018) -
Readability and comprehensibility of informed consent forms for clinical trials
by: Anvita Pandiya
Published: (2010-01-01) -
Readability analysis of informed consent forms for genetic tests in Mexico
by: Beatriz E. de la Fuente-Cortez, et al.
Published: (2021-01-01)