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Before participating in this study, it's crucial to understand the study details and what participation entails. Researchers will provide an informed consent document containing comprehensive information, such as the study's length, required visits, medications, and medical procedures. It also outlines expected outcomes, potential benefits, risks, and additional details. A translator may be available if needed. Researchers will review the informed consent document with you and answer any questions. After gathering all necessary information and discussing it with your family and staff, you can decide whether to participate. If you choose to join, your signature on the informed consent statement confirms your understanding and voluntary agreement. You may withdraw from the study at any time, even after signing.
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