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IRB #: IRB1300335/ CR00012568 Form Approval Date: 2/28/2018 Study Approval Date: 7/12/2013 Study Date of Expiration: 2/27/2019CONSENT TO PARTICIPATE IN A CLINICAL RESEARCH STUDY TITLE: Randomized

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How to fill out informed consent to participate

01

Step 1: Read the informed consent form carefully.

02

Step 2: Understand the purpose and procedures of the study.

03

Step 3: Clarify any doubts or questions with the study investigator.

04

Step 4: Sign and date the consent form to indicate your willingness to participate.

05

Step 5: Keep a copy of the signed consent form for your records.

Who needs informed consent to participate?

01

Informed consent to participate is needed by any individual who is eligible to participate in a research study.

02

This includes both adults and minors, and in some cases, individuals with diminished mental capacity may require a legally authorized representative to provide informed consent on their behalf.

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What is informed consent to participate?

Informed consent to participate is a process where a person is given all the necessary information about a research study or clinical trial before agreeing to participate.

Who is required to file informed consent to participate?

Researchers conducting a study or clinical trial are required to obtain informed consent from potential participants.

How to fill out informed consent to participate?

Informed consent forms typically include information on the purpose of the study, potential risks and benefits, confidentiality, and the participant's rights.

What is the purpose of informed consent to participate?

The purpose of informed consent to participate is to ensure that participants are fully informed about the study and can make an informed decision about whether or not to participate.

What information must be reported on informed consent to participate?

Informed consent forms must include information about the study procedures, risks and benefits, confidentiality, and the participant's rights.

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