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IRB #: STU00202936MODCR0002 Approved by NU IRB for use on or after 12/12/2018Consent to Participate in Research Page 1 of 3Title of Research Study: Virtual Reality Job Interview Training: An Enhancement
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How to fill out institutional review boards

01
To fill out institutional review boards, follow these steps:
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Start by obtaining the necessary forms from your institution's research office.
03
Carefully read all the instructions provided on the forms and make sure you understand them.
04
Gather all the required information and documents that need to be submitted.
05
Fill out the forms accurately and completely. Provide detailed information about the research project, including its purpose, methods, and expected outcomes.
06
Ensure that you address any ethical considerations, such as participant confidentiality and informed consent procedures.
07
Double-check your completed forms for any errors or missing information.
08
Submit the filled-out forms along with any supporting documents to the appropriate institutional review board.
09
Wait for the review board to evaluate your application and provide feedback or approval. Be prepared to make any necessary revisions based on their recommendations.
10
Keep a copy of all the filled-out forms and documentation for your records.
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If your application is approved, proceed with the research project according to the guidelines and conditions set by the institutional review board.

Who needs institutional review boards?

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Institutional review boards are typically required by universities, research institutions, and other organizations that conduct research involving human participants.
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Any research project that involves human subjects, whether it is in the fields of medicine, psychology, sociology, or any other discipline, may need to undergo review by an institutional review board.
03
The purpose of institutional review boards is to ensure the ethical treatment and protection of human participants in research studies.
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By reviewing research protocols, informed consent procedures, and data management plans, these boards help safeguard the rights and well-being of individuals involved in research.
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Institutional Review Boards (IRBs) are committees established to review and approve research involving human subjects, ensuring that ethical standards are met and that participants' rights and welfare are protected.
Researchers who are conducting studies involving human subjects, institutions receiving federal funding, and any organization that performs or sponsors research must file with an Institutional Review Board.
To fill out an Institutional Review Board application, researchers typically need to provide detailed information about the research project, including the study's objectives, methods, participant recruitment strategies, informed consent processes, and measures to protect participant confidentiality.
The primary purpose of Institutional Review Boards is to ensure the protection of human subjects in research by reviewing study protocols and ensuring compliance with ethical standards and regulatory requirements.
Researchers must report information including the study design, potential risks and benefits to participants, informed consent procedures, the selection criteria for participants, and how confidentiality will be maintained.
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