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Before participating in a study, it's crucial to fully understand the process and implications. Researchers will provide an informed consent document containing detailed information about the study, including its duration, required visits, medications, and medical procedures involved. The document outlines expected outcomes, potential benefits, risks, and other relevant details. A translator may be provided if necessary. Researchers will review the document with you and address any questions. After discussing with staff and family, you can decide whether to participate. If you choose to do so, signing the informed consent statement indicates your understanding and voluntary agreement, but you can withdraw from the study at any time for any reason, even after signing.
