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Before participating in a study, it's essential to understand its details and what participation involves. Researchers will provide an informed consent document, which includes information about the study's duration, required visits, medications, and medical procedures. It outlines expected outcomes, potential benefits, risks, and other relevant details. A translator may be available if needed. Researchers will review the document with you and answer any questions. After you have all the necessary information and discussions with staff and family, you can decide whether to participate. If you agree, you'll sign the informed consent statement, affirming your understanding and voluntary participation, with the option to withdraw at any time.