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Before participating in the study, it is essential to understand the details involved. Researchers will provide an informed consent document that outlines the study's length, required visits, medications, and medical procedures. This document also includes expected outcomes, potential benefits, and possible risks. If necessary, a translator may be available. Researchers will discuss the informed consent document with you and address any questions. After gathering all pertinent information and speaking with staff and family, you can decide whether to participate. If you choose to participate, you must sign the informed consent form, indicating your understanding and voluntary agreement. You may withdraw from the study at any time, even after signing.