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Before participating in the study, understanding the details and potential experiences is crucial. Researchers will provide an informed consent document that outlines the study's length, visits, medications, and procedures. It also includes expected outcomes, benefits, risks, and other information. Translators can assist if needed. Researchers will review the document with you, answer questions, and allow time for decision-making. Your voluntary participation requires signing the informed consent statement. Leaving the study is always an option, even after signing.
