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WRITTEN INFORMED CONSENT FORM FOR MINORS Dear Parent, The Department of Education and Science and National Center for Technology in Education have approved a Physical Education Video Project to investigate
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How to Fill Out a Written Informed Consent Form:

01
Begin by carefully reading the entire form to ensure that you understand its contents.
02
Provide your personal information such as your full name, address, contact number, and date of birth in the designated sections.
03
Make sure to complete all required fields, including any checkboxes or information that needs to be accurately filled out.
04
Review the purpose and nature of the study or procedure in which you are consenting to participate. If you have any questions or concerns, seek clarification from the researcher, healthcare professional, or study coordinator before proceeding.
05
Take the time to carefully read and comprehend the potential risks, benefits, and alternatives associated with the study or procedure. If there are any terms or concepts that you are unsure about, don't hesitate to ask for clarification.
06
Sign and date the consent form to indicate your voluntary agreement to participate or undergo the procedure. Note that your signature signifies that you understand the information presented to you and that you have had the opportunity to ask questions.
07
If you are consenting on behalf of someone else, such as a minor or someone unable to provide their own consent, make sure that you have the appropriate legal authority to do so. Provide your relationship to the individual and your contact information if required.
08
Keep a copy of the consent form for your records. It may be useful to refer back to the information or share it with your healthcare provider if needed.

Who Needs a Written Informed Consent Form:

01
Researchers conducting studies or clinical trials are required to obtain written informed consent from individuals participating in their research.
02
Medical professionals or healthcare providers seeking to perform procedures or treatments that involve certain risks or potential side effects often require written informed consent from patients.
03
Institutions, such as hospitals or healthcare facilities, may also require written informed consent from individuals before any medical procedures, surgeries, or treatments are carried out to ensure patient safety and compliance with legal regulations.
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Written informed consent form is a document that explains the risks and benefits of participating in a study or medical procedure, and gives permission to the individual to participate.
Any individual participating in a study or medical procedure is required to file a written informed consent form.
Written informed consent form is typically filled out by the individual or their legal guardian, and involves reading and understanding the document before signing it.
The purpose of a written informed consent form is to ensure that individuals understand the risks, benefits, and implications of their participation in a study or medical procedure.
Written informed consent forms typically include details about the study or procedure, risks and benefits, confidentiality, and the voluntary nature of participation.
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