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Before participating in a study, it's essential to fully understand the process. Researchers will provide an informed consent document containing detailed information about the study's length, required visits, medications, and medical procedures. This document outlines expected outcomes, potential benefits, and risks. A translator may be provided if necessary. Researchers will review the document with you and answer any questions. After discussing with staff and family, you can decide whether to participate. If you choose to participate, signing the informed consent indicates your understanding and voluntary agreement. You can withdraw from the study at any time, even after signing.