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Before participating in the study, it is essential to understand it fully. Researchers will provide an informed consent document that includes details such as study length, number of visits, medications, and procedures. This document also outlines expected outcomes, benefits, risks, and other important information. If needed, a translator can be provided. Researchers will review the document with you, answer your questions, and allow you to decide on participation after talking with your family. Signing the informed consent indicates voluntary agreement to take part in the study, with the option to leave at any time for any reason.