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This document is intended to help researchers confirm that their behavioral research consent forms provide for fully informed consent by participants. More detailed guidance on drafting behavioral
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Use clear and concise language: Avoid using technical jargon or complex terms that may confuse the reader. Instead, use simple and easy-to-understand language.
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Who needs improving readability of consent?

01
Improving readability of consent is beneficial for anyone who needs to understand and provide informed consent. This includes patients or participants in medical research studies, individuals signing legal waivers or contracts, and any other situation where obtaining informed consent is required.

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Improving readability of consent refers to making the language and information in consent forms easier to understand for individuals.
Healthcare providers, researchers, and organizations that collect personal information through consent forms are required to improve readability of consent.
Improving readability of consent can be done by simplifying language, using clear explanations, and providing visual aids to support understanding.
The purpose of improving readability of consent is to ensure that individuals can make informed decisions about their personal information and understand the risks and benefits of providing consent.
Improving readability of consent should include information about the purpose of data collection, potential risks and benefits, how the data will be used, and the individual's rights regarding their personal information.
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