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Before participating in the study, it is crucial to understand what it entails. Researchers will provide an informed consent document detailing the study's duration, visits, medications, procedures, outcomes, benefits, risks, and more. If needed, a translator will be available. After reviewing the document and discussing with staff and family, you can decide whether to participate. Signing the informed consent statement signifies your voluntary agreement. You can choose to leave the study at any time, even after signing the document.
