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INFORMED CONSENT AND ASSUMPTION OF RISK AGREEMENT Alberta Cup 3 & 4, January 2014, Grande Prairie, Alberta By signing this document you will assume certain risks. Please read carefully. This is a
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How to Fill Out Informed Consent and Assumption:

01
Begin by clearly writing the title "Informed Consent and Assumption" at the top of the form.
02
Provide a brief introductory paragraph explaining the purpose and importance of informed consent and assumption.
03
Create a section for the participant's personal information, including their name, contact details, and any relevant identification numbers.
04
Include a section where the participant can indicate their understanding of the nature of the activity, study, or procedure they are agreeing to.
05
Add a section that explains the potential risks and benefits associated with the activity, study, or procedure. The participant should acknowledge that they have been adequately informed about these risks and benefits.
06
Include a section for the participant to confirm that they have had the opportunity to ask questions and have received satisfactory answers.
07
Create a space for participants to indicate their agreement to participate voluntarily and without any coercion. They should also acknowledge that they can withdraw their consent at any time.
08
Provide a section for the participant's signature, along with a space for the date of signing.
09
Leave a section for the researcher, healthcare provider, or responsible party to sign and date, indicating that they have explained the form to the participant.
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Finally, include contact information for any queries or concerns that participants may have.

Who Needs Informed Consent and Assumption?

01
Informed consent and assumption are essential for anyone participating in research studies, clinical trials, or medical procedures. This includes both adults and minors, as well as individuals who may lack decision-making capacity and require a legal guardian or representative.
02
Healthcare providers and researchers must prioritize obtaining informed consent and assumption from their patients or study participants to ensure ethical and legal practices. It is crucial to ensure that individuals fully understand what they are consenting to and the potential risks involved.
03
Informed consent and assumption also play a role in non-medical settings such as educational activities, coaching or training programs, and other situations where individuals are engaging in potentially risky or unfamiliar activities.
Remember, obtaining informed consent and assumption demonstrates respect for autonomy, safeguards participants' rights, and promotes trust between individuals and those responsible for their care or research participation.
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Informed consent is when a person agrees to participate in a study or activity after understanding all the relevant information. Assumption is when a person accepts something as true without proof or confirmation.
Anyone conducting a study or activity that involves human participants is required to obtain and file informed consent and assumption.
Informed consent and assumption forms should be filled out by providing all necessary information about the study or activity, potential risks and benefits, and ensuring that the participant understands and agrees to participate.
The purpose of informed consent and assumption is to ensure that participants are fully aware of what they are agreeing to, the risks involved, and that they are agreeing to participate voluntarily.
Information such as a detailed description of the study or activity, potential risks and benefits, confidentiality procedures, and the right to withdraw from participation should be reported on informed consent and assumption forms.
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