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The informed consent document should succinctly describe the research as it has been presented in the IRB application. Use the second (you) or third person (he/she) to present the study details. Avoid use of the first person (I). Include a statement of agreement at the conclusion of the informed consent document.
I voluntarily agree to take part in this study. I understand I will receive a copy of this consent form. I understand that photographs (audio/video recordings) may be taken during the study. I consent to use of my photograph (audio/video) in presentations related to this study.
Valid informed consent for research must include three major elements: (1) disclosure of information, (2) competency of the patient (or surrogate) to make a decision, and (3) voluntary nature of the decision. US federal regulations require a full, detailed explanation of the study and its potential risks.
The informed consent document should succinctly describe the research as it has been presented in the IRB application. Use the second (you) or third person (he/she) to present the study details. Avoid use of the first person (I). Include a statement of agreement at the conclusion of the informed consent document.
Valid informed consent for research must include three major elements: (1) disclosure of information, (2) competency of the patient (or surrogate) to make a decision, and (3) voluntary nature of the decision.

People also ask

For consent to be valid it must be: voluntary the decision to either consent or not to consent to treatment must be made by the person themselves, and must not be influenced by pressure from medical staff, friends or family.
If you prefer to write your own consent document, you may do so, but be sure to include all required elements of informed consent.
The Elements of Informed Consent. Literature of bioethics often analyzes informed consent in terms of the following elements: (1) disclosure; (2) comprehension; (3) voluntariness; (4) competence; and (5) consent (see U.S. National Commission, 1978, U.S. Presidents Commission, 1982; Meisel and Roth, 1981).
I voluntarily agree to take part in this study. I understand I will receive a copy of this consent form. I understand that photographs (audio/video recordings) may be taken during the study. I consent to use of my photograph (audio/video) in presentations related to this study.
a form signed by a patient prior to a medical procedure to confirm that he or she agrees to the procedure and is aware of any risks that might be involved.

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