PRISM creates guide for improving IC readability

June 2011
Clinical Trials Administrator;Jun2011, Vol. 9 Issue 6, p67
The article offers an overview of a quick reference guide developed by PRISM (Project to Review and Improve Study Materials) to improve readability in informed consent (IC) and other research documents. Some key points discussed include writing in first-person, keeping the sentences short and concise, assessing the reading level, and organizing the information in an easy-to-understand manner.


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