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TA ISO GYMNASTICS CLUB AND GYMNASTICS SASKATCHEWAN INFORMED CONSENT AND ASSUMPTION OF RISK AGREEMENT (To be executed by Participants under the Age of 18) WARNING! Please read carefully By signing
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How to fill out informed consent and assumption

01
Clearly explain the purpose of the study or procedure to the participant.
02
Provide information about any potential risks or benefits involved.
03
Make sure the participant understands the information provided.
04
Have the participant sign the consent form indicating their understanding and agreement to participate.
05
Keep a copy of the signed consent form for your records.

Who needs informed consent and assumption?

01
Informed consent and assumption are needed for any research study involving human participants, medical procedures, clinical trials, and other situations where participants may be at risk.
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Informed consent is a process for getting permission before conducting a healthcare intervention on a person, whereas assumption is a belief or statement taken for granted without proof.
Healthcare providers and researchers are required to obtain and file informed consent and assumption from patients or participants.
Informed consent and assumption forms can be filled out by providing all necessary information, risks, benefits, and alternatives associated with the intervention, and obtaining the signature of the patient or participant.
The purpose of informed consent and assumption is to ensure that individuals are fully informed about the healthcare intervention they are receiving, including any potential risks or benefits.
Information such as the nature of the intervention, risks involved, benefits, alternatives, and the patient's consent must be reported on the informed consent and assumption form.
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