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PARTICIPANTS INFORMED CONSENT FORM Alberta Rhythmic Sportive Gymnastics Federation (AR SGF) Operating as RHYTHMIC GYMNASTICS ALBERTA (RGA) Please check: Gymnast Coach in Training Coach Judge Volunteer
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How to fill out participant's informed consent form:

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Begin by reading the entire form carefully. This will ensure that you understand all the information and requirements outlined in the form.
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Fill in your personal information accurately. This may include your name, address, contact number, and any other relevant details needed.
03
Make sure to carefully read through all the terms and conditions mentioned in the form. This section will outline the purpose of the study, the potential risks and benefits involved, and any expected time commitments.
04
If you have any questions or concerns regarding the study or the consent form, it is essential to clarify them with the researcher or study coordinator. They will be able to provide you with any additional information required.
05
After fully understanding the study and its implications, give your consent by signing and dating the form. This indicates that you willingly agree to participate in the study, understanding its objectives, and any potential risks involved.

Who needs the participant's informed consent form:

01
Researchers: Researchers conducting a study with human participants are required to obtain informed consent from all individuals involved. This ensures that participants are aware of the purpose, potential risks, and benefits of the study before deciding to participate.
02
Institutional Review Boards (IRBs): IRBs review and approve research studies involving humans to ensure they are conducted ethically and with the participants' welfare in mind. They require a detailed informed consent form to be submitted for their evaluation and approval.
03
Participants: It is crucial for participants to receive and sign the informed consent form before participating in any research study. This allows them to make an informed decision about their involvement and ensures their rights and safety are protected.
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Participant's informed consent form is a document that explains the research study, its purpose, risks, benefits, and procedures to the participant in a clear and understandable manner.
The researcher or the organization conducting the research study is required to file participant's informed consent form.
Participant's informed consent form can be filled out by providing all necessary information about the research study, risks, benefits, and procedures to the participant and obtaining their signature.
The purpose of participant's informed consent form is to ensure that the participant understands the research study, its risks, benefits, and procedures before agreeing to participate.
Participant's informed consent form must include information about the research study, risks, benefits, procedures, confidentiality, and the right to withdraw from the study.
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