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Before participating in the study, it is important to understand it fully. Researchers will provide an informed consent document that details the study, including length, visits, medications, and procedures. The document also outlines expected outcomes, benefits, risks, and other details. If needed, a translator can be provided. After reviewing the document and discussing with researchers and family, you can decide whether to participate. Signing the informed consent indicates voluntary participation, with the option to leave at any time for any reason.
