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Er1 1 RTI International, 3040 Cornwallis Road, Research Triangle Park, NC 27709, wav, rhubal, studer, sparrow rti.org 2 University of North Carolina at Wilmington, 601 South College Road, Wilmington, NC 28403, guinnc uncw.edu 3 Duke University, Box 90085, Durham, NC 27708, ruthday duke.edu Abstract We developed an application using synthetic character technology to allow users to practice administering informed consent. The target audience for this application is health communications resea.
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Stredney FAQ
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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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Informed Consent Checklist (1998) A statement that the study involves research. An explanation of the purposes of the research. The expected duration of the subject's participation. A description of the procedures to be followed. Identification of any procedures which are experimental.
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The informed consent process involves three key features: (1) disclosing to potential research subjects information needed to make an informed decision; (2) facilitating the understanding of what has been disclosed; and (3) promoting the voluntariness of the decision about whether or not to participate in the research.
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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. President's Commission, 1982; Meisel and Roth, 1981).
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I have read and understand the information in this form. I have been encouraged to ask questions and all of my questions have been answered to my satisfaction. I have also been informed that I can withdraw from the study at any time. By signing this form, I voluntarily agree to participate in this study.
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Informed consent is a process of communication between you and your health care provider that often leads to agreement or permission for care, treatment, or services. Every patient has the right to get information and ask questions before procedures and treatments.
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To achieve truly informed consent, four criteria have been identified: Information disclosure. Competence. Comprehension. Voluntariness.
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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.
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Attachment 1
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by FK Dankar · 2019 · Cited by 103 — Informed consent in medical care is generally...
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by NM Kettle · 2002 · Cited by 4 — (a synthetic form of hormone ... partly responsible...
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Apr 16, 2019 — Your information will only be used in accordance with this authorization...
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Attachment 1
FOR ALL RESEARCH CONDUCTED UNDER THIS ASSURANCE, THE IRB CHAIRPERSON. HEREBY ATTESTS THAT...
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In order to guarantee people's right to know, we wrote an informed consent for...
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Capacity to make a fully informed decision and to consent for treatment;.
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