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FOR IRB USE ONLY IRB ID #: 201707154 APPROVAL DATE: 08/29/17 RELEASED DATE: 10/02/17 EXPIRATION DATE: 08/01/18INFORMED CONSENT DOCUMENT Aim 2 Participants Project Title: Development and validation

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Read the informed consent document carefully to understand the information provided.

02

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Who needs informed consent documentaim 2?

01

Anyone who is participating in a research study or clinical trial related to aim 2 needs to fill out the informed consent document.

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What is informed consent documentaim 2?

Informed consent documentaim 2 is a formal document that ensures participants are fully informed about the nature of a study and their involvement in it, including potential risks and benefits.

Who is required to file informed consent documentaim 2?

Researchers and organizations conducting studies involving human subjects are required to file informed consent documentaim 2.

How to fill out informed consent documentaim 2?

To fill out informed consent documentaim 2, include participant information, the purpose of the study, procedures involved, potential risks, benefits, and confidentiality assurances, and have it signed by the participant.

What is the purpose of informed consent documentaim 2?

The purpose of informed consent documentaim 2 is to protect the rights and welfare of participants in research studies by ensuring they understand what participation entails.

What information must be reported on informed consent documentaim 2?

Information that must be reported includes the study's purpose, procedures, risks, benefits, confidentiality measures, and the right to withdraw from the study at any time.

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