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OBJECTIVES/SPECIFIC AIMS: Develop a plain language informed consent template that met IRB and regulatory requirements. Evaluate the effectiveness of the template at improving the readability of informed consents. Field test the informed consent with low health literacy. METHODS/STUDY POPULATION: We...

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Váldodahkkit: Tina Moore, Laura P. James, Jennifer Holland, Edith Paal, Kristie Hadden
Materiálatiipa: Artihkal
Giella:English
Almmustuhtton: Cambridge University Press 2017-09-01
Ráidu:Journal of Clinical and Translational Science
Liŋkkat:https://www.cambridge.org/core/product/identifier/S205986611700187X/type/journal_article