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Before participating in the study, it is crucial to fully comprehend it and what involvement may entail. Researchers will provide an informed consent document detailing study particulars such as duration, visits required, medications, and procedures involved. The document outlines expected outcomes, potential benefits, risks, and other necessary details. Translation services may be available as needed. Researchers will go over the document with you, address any inquiries, and, after gathering necessary information and conferring with loved ones, you can decide on participation. Signing the informed consent affirms your understanding of the study and willingness to participate voluntarily. You retain the option to exit the study at any point and for any reason, even subsequent to signing the informed consent form.
