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INFORMED CONSENT AGREEMENT for participants under 19 years Dear Registrant/ Parent/Guardian: Thank you for choosing to use the services or programs of Recreation Integration Victoria and/or Disabled
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How to fill out informed consent agreement

01
To fill out an informed consent agreement, follow these steps:
02
Read the agreement thoroughly, understanding all the terms and conditions.
03
Provide your personal information, such as your full name, address, contact details, and date of birth.
04
Understand the purpose and nature of the study or procedure you are giving consent for.
05
Ask any questions or seek clarification on any doubts you may have before signing the agreement.
06
Sign and date the informed consent agreement.
07
Keep a copy of the signed agreement for your records.
08
If applicable, provide the contact information of a trusted person who can make decisions on your behalf, known as a healthcare proxy or power of attorney.
09
Make sure to receive a signed copy of the agreement from the researcher or healthcare professional.

Who needs informed consent agreement?

01
Anyone who is participating in a research study, medical procedure, clinical trial, or any situation where their personal information or rights might be involved needs an informed consent agreement. This includes both adults and minors (with parental or guardian consent). Informed consent ensures that individuals understand the risks, benefits, and potential outcomes of the activity they are consenting to and protects their rights as participants.
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An informed consent agreement is a document signed by a patient or research subject, acknowledging that they have been fully informed about the risks and benefits of a medical treatment or research study.
Medical professionals, researchers, or institutions conducting medical treatments or research studies are required to have patients or subjects sign informed consent agreements.
Informed consent agreements should be filled out with clear and easy-to-understand language, detailing the nature of the treatment or study, associated risks and benefits, and the patient's or subject's rights.
The purpose of an informed consent agreement is to ensure that patients or research subjects are fully aware of what they are agreeing to, and to protect their rights and well-being.
Informed consent agreements must include details about the treatment or study, risks and benefits involved, alternative options, confidentiality agreements, and the right to withdraw consent.
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