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Vanderbilt University Institutional Review Board Informed Consent Document for Research Principal Investigator: Rogers Hall Study Title: Bridging Spaces for Learning in Urban Extended Spaces Institution/Hospital:

How to fill out this informed consent document

How to fill out this informed consent document:

1. Read the document thoroughly: Before filling out the informed consent document, take the time to read it carefully. Understand the purpose, risks, benefits, and any other important information mentioned in the document.
2. Provide accurate personal information: Fill in your personal details accurately, including your full name, address, phone number, and email address. Ensure that this information is up to date and can be used for communication purposes if needed.
3. Understand the treatment or procedure: Make sure you have a clear understanding of the treatment or procedure that requires informed consent. Research and ask questions to your healthcare provider if anything is unclear or if you require further information.
4. Sign and date the document: Once you have read and understood the document, sign it at the designated space provided. Always date it as well to indicate when the consent was given. This signature verifies that you have willingly provided informed consent.

Who needs this informed consent document?

1. Patients undergoing medical procedures or treatments: The informed consent document is primarily required for patients who are about to undergo medical procedures or treatments. This ensures that they are aware of the potential risks and benefits and have made an informed decision about their healthcare.
2. Clinical trial participants: Individuals participating in clinical trials also need to sign informed consent documents. It helps them understand the purpose, procedures, risks, and benefits of the trial before they agree to participate.
3. Minors and their legal guardians: When a medical procedure involves a minor, their parents or legal guardians will be required to sign the informed consent document on their behalf. This is to ensure that the responsible adult is fully aware of the treatment or procedure and can provide consent on behalf of the child.
4. Research subjects: Individuals involved in research studies or experiments may also need to provide informed consent. This allows them to fully understand the purpose and risks of the research before voluntarily participating.

In conclusion, filling out an informed consent document requires reading and understanding the document, providing accurate personal information, signing and dating it, and is typically necessary for patients undergoing medical procedures, clinical trial participants, minors and their legal guardians, and research subjects.

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What is this informed consent document?

This informed consent document is a legal document that provides information about a research study and outlines the risks and benefits of participating.

Who is required to file this informed consent document?

Researchers conducting a study are required to file this informed consent document with their institution's review board.

How to fill out this informed consent document?

This informed consent document is typically filled out by the researcher and reviewed by the study participant before they agree to participate.

What is the purpose of this informed consent document?

The purpose of this informed consent document is to ensure that participants are fully informed about the study and give their voluntary consent to participate.

What information must be reported on this informed consent document?

This informed consent document must include information on the study's purpose, procedures, risks, benefits, alternatives, confidentiality, and contact information for questions or concerns.