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Before participating in a study, it’s essential to understand its details, which are provided in an informed consent document. This document outlines the study's duration, required visits, medications, and medical procedures involved. It also includes expected outcomes, potential benefits, possible risks, and other relevant information. A translator may be provided if necessary. Researchers will review the document with participants and answer questions. After discussing with family and staff, individuals can decide whether to participate. If choosing to proceed, participants must sign the informed consent statement, indicating they understand and agree to participate voluntarily. They can withdraw from the study at any time, even after signing.