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Before participating in a study, it is crucial to understand the study's details and what participation entails. Researchers will provide an informed consent document outlining the study's length, required visits, medications, and medical procedures involved. This document also covers expected outcomes, potential benefits, and risks. If necessary, a translator may be available. Researchers will review the informed consent document with participants and address any questions. After gathering all necessary information and discussing it with family and staff, participants can decide whether to join. If they choose to participate, signing the informed consent indicates their understanding and voluntary agreement, though they can withdraw at any time for any reason.