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GYMNASTICS ONTARIO INFORMED CONSENT AND ASSUMPTION OF RISK AGREEMENT (To be executed by Participants under 18 years old) WARNING! Please read carefully By signing this document, you will assume certain

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How to fill out participant informed consent and

01

Identify the key information that needs to be included in the informed consent form.

02

Create a clear and concise document that explains the purpose of the research, the procedures involved, the risks and benefits, and the participant's rights.

03

Provide space for the participant to sign and date the form, indicating their understanding and agreement to participate voluntarily.

04

Ensure that the participant is given enough time to read and ask questions about the informed consent form before signing.

05

Make sure to provide a copy of the signed form to the participant for their records.

Who needs participant informed consent and?

01

Anyone conducting research involving human participants

02

Medical professionals performing experimental treatments or procedures on patients

03

Educators conducting research on students

04

Organizations conducting surveys or studies involving human subjects

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What is participant informed consent and?

Participant informed consent is a process in which participants are fully informed about the research study and voluntarily agree to participate.

Who is required to file participant informed consent and?

Researchers conducting a study involving human participants are required to obtain and file participant informed consent.

How to fill out participant informed consent and?

Participant informed consent forms are typically filled out by researchers and reviewed with potential participants before they agree to participate.

What is the purpose of participant informed consent and?

The purpose of participant informed consent is to protect the rights and welfare of research participants by ensuring they understand the study and voluntarily agree to participate.

What information must be reported on participant informed consent and?

Participant informed consent forms must include details about the study purpose, procedures, risks and benefits, confidentiality, and contact information.

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