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State Science and Engineering Fair of Florida Verification of Informed Consent Form VICE (assent or consent) For a Human Participants Research Study This form confirms the number of human participants

How to fill out verification of informed consent

How to fill out verification of informed consent:

1. Start by carefully reading the entire informed consent form. Make sure you understand all the information and requirements.
2. Fill in your personal information, such as your name, contact details, and any other requested details.
3. Review the purpose or objective of the study or procedure mentioned in the informed consent form.
4. Read all the risks and benefits associated with the study or procedure. Make sure you fully understand the potential outcomes and any possible complications.
5. If there are any special instructions or requirements, ensure that you follow them correctly. This could include fasting before a medical procedure or avoiding certain medications.
6. If you have any questions or concerns, don't hesitate to ask the researcher or medical professional providing the informed consent form. They are there to help clarify any doubts you may have.
7. Sign and date the verification of informed consent section. This signifies that you have read and understood the information presented to you.
8. If there are any additional witnesses required, ensure that they also sign and provide their information in the appropriate sections.
9. Retain a copy of the fully completed informed consent form for your own records.

Who needs verification of informed consent?

1. Individuals participating in research studies: Informed consent is crucial for those participating in any form of research, be it medical, scientific, or social.
2. Patients undergoing medical procedures: Consent must be obtained before conducting any medical intervention or procedure, ensuring that the patient fully understands the potential risks and benefits involved.
3. Participants in clinical trials: Before enrolling in a clinical trial, participants must provide informed consent, as they will be subject to experimental treatments and monitoring.

NOTE: It is essential to consult with legal and/or medical professionals for specific requirements and guidelines related to verification of informed consent in your jurisdiction.

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