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A consent form is a signed document that outlines the informed consent of an individual for a medical study, clinical trial, or activity.
I have read and I understand the provided information and have had the opportunity to ask questions. I understand that my participation is voluntary and that I am free to withdraw at any time, without giving a reason and without cost. I understand that I will be given a copy of this consent form.
Ensure your consent document follows these general guidelines: Use the IRB consent form templates. Write at an eighth-grade reading level and use lay language vs. Avoid legalistic language. Use gender-inclusive language. Use the correct forms for parental permission and child assent. Give each consent a unique name in iRIS.
Your participation in this study is voluntary. It is up to you to decide whether or not to take part in this study. If you decide to take part in this study, you will be asked to sign a consent form. After you sign the consent form, you are still free to withdraw at any time and without giving a reason.
Obtaining Written or Verbal Informed Consent. Obtaining consent involves explaining the research and assessing participant comprehension using a consent document, usually a written consent form or information sheet, as a guide for the verbal explanation of the study.
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Effective informed consent discussion involves multiple stages, which include: establishing rapport with the patient, obtaining permission for the discussion, preparing the listener, gathering information about the patients perspective, providing information about the clinical research, and discussion of next steps.

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