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Study ID:UMCIRB 17001242 Date Approved: 9/21/2021 Expiration Date: 4/17/2022Informed Consent to Participate in Research Information to consider before taking part in research that has no more than

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How to fill out informed consent to participate

01

Read the informed consent form carefully to understand all the terms and conditions.

02

Fill out your personal information accurately, including your name, contact information, and any other required details.

03

Sign and date the form to indicate your agreement to participate in the activity or study.

04

Ask any questions you may have before signing the consent form to ensure you fully understand what you are agreeing to.

Who needs informed consent to participate?

01

Anyone who wants to participate in a research study, clinical trial, medical procedure, or any other activity that requires informed consent.

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What is informed consent to participate?

Informed consent to participate is the voluntary agreement to take part in a research study after being informed about all aspects of the study.

Who is required to file informed consent to participate?

Researchers conducting the study are required to obtain and file informed consent from each participant.

How to fill out informed consent to participate?

Informed consent forms are typically filled out by the researcher, who explains the study, risks, benefits, and participant rights to the potential participant.

What is the purpose of informed consent to participate?

The purpose of informed consent is to ensure that participants are aware of the study details, risks, benefits, and rights before deciding to participate.

What information must be reported on informed consent to participate?

Informed consent forms must include study details, potential risks and benefits, participant rights, confidentiality measures, and contact information for questions or concerns.

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