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Evaluation of Readability of Consent Forms on the Understanding of the Information Received by Volunteers

Language Clinical Trial

Official title:
Evaluation of the Readability of Information and Consent Forms on the Understanding of the Information Received by Participants in Biomedical Research

Clinical Trial Summary

Prior to the completion of biomedical research, any person undergoing it must receive a readable and intelligible information about this research, in order to give free and informed consent. The willingness to inform patients of all risks and constraints related to research may be in contradiction with the need to write informative and concise documents that are understandable to research participants. As a result, consent forms are long, contain a lot of information and are complicated to understand.

The objective of this study is to evaluate the impact of the readability of the information and consent forms on the understanding of the information received by participants in clinical trials.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03105752
Study type Interventional
Source Groupe Hospitalier Pitie-Salpetriere
Contact
Status Completed
Phase N/A
Start date April 2014
Completion date April 2016
View Details
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