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Human Subjects

 

Institutional Review Board (IRB)

The purpose of ÌÇÐÄ´«Ã½'s Institutional Review Board (IRB) is to ensure the protection of the rights and welfare of all human subjects that participate in research. Research conducted by faculty, staff, and students must be approved by the IRB, prior to research being conducted, as required by federal, state, and University regulations. The IRB reviews research applications and proposals involving human subjects to ensure the rights of the subjects are not violated and that the research conforms to the Code of Federal Regulations. The committee then approves, request revisions, or determines that the protocol does not fall under human subjects research. 

Researchers are required to complete the CITI Responsible Conduct of Research (RCR) training certification before a protocol will be approved.  Additional information is below.

When you have completed the study, please complete the . You may also request an amendment or renewal of your protocol through the website. It is required to document the number of subjects in your study and any adverse events the subjects experienced.  For instructions on completing and submitting applications, please view the Institutional Review Board 101 PowerPoint in the Forms and Resources page.

Points of Consideration Before Submitting a Protocol

IRB Application Forms

Students completing a hearing assessment

Determination of Research Form

This form will help to determine if a project will fall under the federal definition of research for human subjects.  At a minimum, all researchers presenting findings outside of the classroom must complete the DOR form and receive an approval letter from the IRB before starting their project. 

Students meeting to work on a project.

Exempt Application

This should be completed if research subjects will remain anonymous/confidential, there is no intervention, and minimal risk to subjects.

Exempt App

Students completing a medical assessment

Expedited or Full Review Application

Expedited Review is typically for research which has identifiable information, an intervention and minimal risk. A Full Review addresses research that is associated with greater than minimal risks or includes protected populations.

Expedited/Full App

 

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