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Before participating in a study, it's crucial to understand the study and participation expectations. Researchers will provide an informed consent document detailing the study's length, required visits, medications, and procedures. It also outlines expected outcomes, potential benefits, and risks. A translator may be available if needed. Researchers will review the document with you and answer any questions. After gathering all necessary information and discussing with staff and family, you can decide on participation. If you choose to participate, signing the informed consent statement signifies your understanding and voluntary agreement, and you can withdraw from the study at any time for any reason, even after signing.