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This document is a consent form for participants in the functional imaging study investigating brain activity associated with shape representation and object perception using fMRI.
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How to fill out Consent Form (I. Biederman): Functional Imaging Studies of Shape Representation

01
Read the consent form thoroughly to understand the study's purpose and procedures.
02
Fill out your personal information, including your name and contact details, where indicated.
03
Review the potential risks and benefits outlined in the form.
04
If you have any questions, ask the research team for clarification before proceeding.
05
Indicate your consent by signing and dating the form at the designated area.
06
Keep a copy of the signed consent form for your records.

Who needs Consent Form (I. Biederman): Functional Imaging Studies of Shape Representation?

01
Participants involved in the Functional Imaging Studies of Shape Representation.
02
Researchers conducting the study who require informed consent from participants.
03
Ethics review boards overseeing the study for compliance and participant rights.
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The Consent Form for the Functional Imaging Studies of Shape Representation is a document that outlines the nature of the study, the procedures involved, and the rights of participants. It ensures that participants are fully informed about what they are consenting to before participating in the research.
Participants involved in the Functional Imaging Studies of Shape Representation are required to file the Consent Form. This includes all individuals who will be taking part in the study and undergoing the imaging procedures.
To fill out the Consent Form, participants should read through the entire document carefully, understand the information provided, and then sign where indicated. They may also need to provide additional personal information as requested in the form.
The purpose of the Consent Form is to obtain informed consent from participants, ensuring they are aware of the study's aims, potential risks, and their rights, including the right to withdraw from the study at any point.
The information that must be reported on the Consent Form includes the study's purpose, procedures, potential risks and benefits, confidentiality assurances, and contact information for the research team, as well as a statement about the participant's rights.
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