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Before participating in a study, it's crucial to understand its details and what involvement entails. Researchers provide an informed consent document that includes information about the study's duration, number of visits, medications, and medical procedures. It outlines expected outcomes, potential benefits, risks, and more. If necessary, a translator may be available. Researchers will explain the document and answer any questions you may have. After discussing the information with staff and family, you can decide whether to participate. If you choose to participate, you'll sign the informed consent statement, which indicates that you understand the study and agree to participate voluntarily. You can withdraw from the study at any time, even after signing the consent.