Impact of Readability Improvements on the Comprehension of Written Information Given to Clinical Trial Patients: a RCT

Category Primary study
Registry of Trialsclinicaltrials.gov
Year 2009
The principle objective of this randomised controlled trial is to assess whether an improvement in lexico-syntactic readability combined with adherence to French recommendations for good practice in writing the Information and Consent Form (ICF) given to patients participating in clinical trials, increases their understanding of the information compared to conventional written information, in real (not simulated) conditions.
Epistemonikos ID: 31d795ea54f4c1d59adbdb91f2e4dc512d0e6ede
First added on: May 05, 2024