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Study ID: HUM00093760 IRB: IRB MED Date Approved: 9/20/2023 Expiration Date: 9/7/2024UNIVERSITY OF MICHIGAN CONSENT TO BE PART OF A RESEARCH STUDY 1. KEY INFORMATION ABOUT THE RESEARCHERS AND THIS
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How to fill out fmri consent forms

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How to fill out fmri consent forms

01
Read the entire consent form carefully to understand the study and your rights.
02
Ensure you understand the purpose of the fMRI study and the procedures involved.
03
Verify the potential risks and benefits mentioned in the form.
04
Fill out your personal information as required, including your name, date of birth, and contact details.
05
Answer any medical history questions honestly to ensure your safety during the fMRI.
06
Indicate your consent by signing and dating the form as instructed.
07
Ask questions if any part of the consent form is unclear before finalizing your signature.

Who needs fmri consent forms?

01
Anyone participating in an fMRI study requires a consent form.
02
Researchers conducting the study need consent forms to comply with ethical guidelines.
03
Institutional review boards or ethics committees require consent forms for oversight.
04
Patients or volunteers in clinical trials involving fMRI must complete consent forms.
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fMRI consent forms are documents that provide information to participants about an fMRI study, detailing the procedure, risks, benefits, and their rights, which participants must agree to before participating.
Researchers and institutions conducting fMRI studies are required to file fMRI consent forms for each participant involved in the research.
To fill out fMRI consent forms, participants should read the entire document carefully, ask any questions they may have, and then sign and date the form to indicate their voluntary agreement to participate.
The purpose of fMRI consent forms is to ensure that participants are well-informed about the study, understand the risks and benefits, and consent to their participation voluntarily.
fMRI consent forms must report details such as the study's purpose, procedures, duration, potential risks, benefits, confidentiality measures, and contact information for questions.
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