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CURLING CANADA INFORMED CONSENT AND ASSUMPTION OF RISK AGREEMENT (To be executed by Participants under the Age of Majority) WARNING! By executing this document you will assume certain risks and responsibilities.
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Who needs informed consent and assumption?

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Informed consent and assumption are required for individuals who are participating in certain activities, experiments, medical procedures, or research studies. It ensures that the person involved understands the risks, benefits, and possible outcomes of their involvement. This includes patients, participants in scientific research, individuals undergoing medical treatments or procedures, and anyone else who might be affected by the process.
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Informed consent is the process by which a participant voluntarily confirms their willingness to participate in a study after being informed of all relevant facts, including risks, benefits, and alternatives. Assumption refers to the conditions or understandings that are accepted as true without proof, often in relation to the expectations of outcomes based on the informed consent.
Researchers and institutions conducting studies involving human subjects are required to file informed consent and assumption forms to ensure the ethical treatment of participants.
To fill out informed consent and assumption, researchers should provide clear, concise information about the study, including its purpose, procedures, possible risks and benefits, and the participant's rights. Participants should sign the form indicating their understanding and agreement.
The purpose of informed consent and assumption is to protect the autonomy of participants, ensuring they are fully aware and agree to the study's conditions before participating, thereby promoting ethical research practices.
The information reported must include the study's purpose, procedures, risks, benefits, confidentiality measures, and the right to withdraw at any time without penalty.
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