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VCU IRB PROTOCOL NUMBER: HM20019583RESEARCH PARTICIPANT INFORMATION AND CONSENT FORM STUDY TITLE: Bundle Consent and Expectation Setting in Pediatric Intensive Care Unit (PICU) VCU INVESTIGATOR: Nikki

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How to fill out consent document for irb

01

Obtain a copy of the consent document template from your IRB.

02

Begin with the title of the study at the top of the document.

03

Include the name and contact information of the principal investigator.

04

Provide a clear description of the study's purpose in layman's terms.

05

Outline the procedures involved in the study, including any risks and benefits.

06

Detail how participant confidentiality will be maintained.

07

Include information about voluntary participation and the right to withdraw.

08

Add a section on compensation, if applicable.

09

Provide an area for participants to ask questions and obtain answers.

10

Conclude with spaces for participant signatures and dates.

Who needs consent document for irb?

01

Researchers conducting studies involving human subjects.

02

Institutions and organizations that require ethical oversight for research.

03

Participants in studies who must be informed about their rights and the nature of the study.

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What is consent document for irb?

A consent document for IRB is a formal agreement that outlines the rights and responsibilities of research participants and provides them with information about the study, including its purpose, procedures, risks, and benefits.

Who is required to file consent document for irb?

Researchers conducting studies that involve human subjects are required to file a consent document with the Institutional Review Board (IRB). This includes academic researchers, clinicians, and any other entities conducting research that needs ethical review.

How to fill out consent document for irb?

To fill out a consent document for IRB, researchers should include essential elements such as the study's purpose, risks and benefits, confidentiality assurances, and participant rights. It is important to use clear, jargon-free language and ensure that the document is structured in a way that is easy to understand.

What is the purpose of consent document for irb?

The purpose of the consent document for IRB is to ensure that participants are fully informed about the research study and give their voluntary consent. It aims to protect participants' rights and welfare by ensuring they understand their involvement in the study.

What information must be reported on consent document for irb?

The consent document must report information including the study's purpose, study procedures, potential risks and benefits, confidentiality measures, voluntary participation, and contact information for questions or concerns. It may also include information on how participants can withdraw from the study.

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