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Before participating in a study, it's crucial to fully grasp the details. Researchers will assist by presenting an informed consent document, which covers study specifics like duration, visits, medications, and procedures. The document also outlines expected outcomes, benefits, risks, and other information. If needed, a translator can aid in understanding the document. After reviewing the information and consulting with family and staff, you can make an informed decision on participation. Signing the informed consent indicates understanding and voluntary agreement, with the freedom to exit the study at any point, even after signing.