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ORA: 18080302IRB01 Date IRB Approved: 9/26/2018 Expiration Date: 9/26/2019Investigator: Dr. Kern Singh Contact Information: 1611 W Harrison Suite #300 Chicago, IL 60612 (312) 4322435 Title of Study:

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How to fill out consent to take part

01

Start by providing your personal information such as name, age, address, and contact details.

02

Read the consent form carefully to understand the purpose, procedures, and potential risks involved in participating.

03

If you have any questions or concerns, consult with the research team or a healthcare professional.

04

Sign and date the consent form to indicate your voluntary agreement to participate.

05

Keep a copy of the signed consent form for your records.

Who needs consent to take part?

01

Anyone who wishes to participate in a research study or any activity that requires informed consent needs to fill out a consent form.

02

This includes individuals of legal age and mental capacity to understand the nature of the study and its implications.

03

In cases involving minors or individuals with limited decision-making capacity, a parent, guardian, or authorized representative may need to provide consent on their behalf.

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What is consent to take part?

Consent to take part is a formal agreement given by an individual to participate in a specific activity or research study.

Who is required to file consent to take part?

Any individual who wishes to participate in the activity or research study is required to file consent to take part.

How to fill out consent to take part?

Consent to take part can be filled out by providing personal information, agreeing to the terms and conditions, and signing the document.

What is the purpose of consent to take part?

The purpose of consent to take part is to ensure that individuals understand the risks and benefits associated with participating in the activity or research study, and to give their voluntary agreement to take part.

What information must be reported on consent to take part?

Consent to take part must include details about the activity or research study, potential risks and benefits, contact information for questions, and a signature from the individual giving consent.

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