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Before participating in the study, it’s crucial to understand its details and what participation entails. Researchers will provide an informed consent document, which includes information about the study’s duration, visit requirements, medications, and 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 discussing with staff and family, you can choose to participate by signing the consent statement, indicating your understanding and voluntary agreement. You may withdraw from the study at any time for any reason, even after signing.