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Nov 6, 2023 · Where alterations to standard consent procedures have been used, debriefing must be provided to participants at the end of their involvement in the study. Researchers must explain why participants were temporarily led to believe that the research, or some aspect of it, had a different purpose, or why participants received less than full disclosure.
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This template is a guide to assist researchers applying to the Health Canada-PHAC REB. It should not be interpreted as a standard for other institutions. This template follows the guidance provided in TCPS 2 (Chapter 3: The Consent Process) which is the official human research ethics policy of the Canadian federal research granting agencies. Resear...
This template is a guide to assist researchers applying to the Health Canada-PHAC REB. It should not be interpreted as a standard for other institutions. This template follows the guidance provided in TCPS 2 (Chapter 3: The Consent Process) which is the official human research ethics policy of the Canadian federal research granting agencies. Resear...
These forms were created using the REB Secretariat's consent form template as a guide. They are meant to assist researchers applying to the Health Canada-PHAC REB and should not be interpreted as a standard for other institutions. The forms follow the guidance provided in TCPS 2 (Chapter 3: The Consent Process) which is the official human research ...
This form was created using the REB Secretariat's assent form template as a guide. It is meant to assist researchers applying to the Health Canada-PHAC REB and should not be interpreted as a standard for other institutions. The form follows the guidance provided in TCPS 2 (Chapter 3: The Consent Process) which is the official human research ethics ...
In the context of an earlier intervention study that we conducted comparing three different consent procedures for the use of residual tissue for scientific research , we perused the literature for examples of other studies in which consent was waived, and the conditions under which such a waiver was applied. Most of the literature that we found was focused on only one subset of reasons, or ...
The use of research directives does not alter the requirements for consent as articulated by the provisions of this Policy. In particular, in accordance with Article 3.9, researchers are required to seek the consent of authorized third parties before individuals who lack decision-making capacity can participate in research. If an individual ...
The other new requirement is to begin the consent form with a brief and focused summary of the information that is most relevant to the decision-making process. 6 The summary should include a statement that the subject's participation is voluntary, an explanation of the purpose of the research, and a description of the procedures, as well as ...
this way, participants can provide their consent to be temporarily deceived and informed later—a process known as “authorized deception”[5].However,the mere act of knowing that one is being observed through research can change the outcome of a study (termed the Hawthorne effect) [5]. Thus, the use of authorized
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How do I adapt the informed consent process to potential participants?
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The informed consent process in clinical studies. The guidelines, which supplement existing informed consent documentation, introduce novel recommendations in three directions: the adaptation of the informed consent process to potential participants; the improvement of the participant's experience; and the use of new tools to guide the informed consent process.
