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This section provides researchers an overview of the key considerations regarding the process for obtaining consent or assent from research participants, as well as templates and sample forms for obtaining their consent or assent.
Researchers may request an alteration to consent requirements if they can meet the criteria of Article 3.7A. These include a requirement to satisfy the research ethics board (REB) that it is impossible, impracticable (see Glossary) or inappropriate to address the research question without the requested alteration.
May 5, 2021 · All prospective participants must have the opportunity to give informed consent before entering a research project (see TCPS2 (2018) Chapter 3); however, a signed consent form is not always necessary (TCPS2 (2018) Articles 3.12 and 10.2).
If you choose to obtain oral consent from participants, rather than by asking them to sign a written / hard copy consent form, you must document the consent process in an alternative manner.
Individuals conducting research involving human participants must ensure that their participants provide voluntary, informed, and ongoing consent. In some cases, where consent from participants is not applicable (see Section 4 below) researchers must obtain assent from their participants.
In the majority of cases, where a written-and-signed approach to consent is used, the information letter and consent form are best presented as one document. The information letter should begin with an invitation to potential participants and should explain why they have been asked to participate.
People also ask
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Participation in research means agreeing to share information with researchers. This information may help researchers answer their research questions or meet their research goals. The answers to research questions can only come from information provided by research participants.
