If you have a research proposal, follow the Decision Tree to determine whether IRB approval is necessary, and if so, whether the activity requires expedited or full IRB review.
- If the research is a non-reviewed activity, no action is required.
- If the research qualifies for an exemption, submit a full proposal (without a literature review) and one typed original of Form G to the IRB.
- If the research qualifies for an expedited review, submit a full proposal (including Forms A-F) to the IRB by email.
- If the research requires a full board review, submit a full proposal (including Forms A-F) to the IRB by email.
- If you have questions about which category applies to your project, please contact the IRB chair.
Please submit your applications as Word or PDF files in an email to the IRB at email@example.com.
- All IRB Forms (Forms A-G and Appendices)
- IRB Form A: Research Proposal Format
- IRB Form B: Consent Form (Adults)
- IRB Form C: Short Consent Form (Adults)
- IRB Form D: Parent/Guardian Permission Form
- IRB Form E: Assent Form for Minors
- IRB Form F: IRB Approval Notification Form
- IRB Form G: Notification to IRB of Exempt Research Activities
Examples of Risk
Physical discomfort, pain, injury, illness or disease brought about by the methods and procedures of the research.
May be experienced during the research situation and/or later, as a result of participating. Includes anxiety, stress, fear, confusion, embarrassment, depression, guilt, shock, loss of self-esteem, altered behavior.
Alterations in relationships with others that are to the disadvantage of the subject, including embarrassment, loss of respect of others, labeling with negative consequences, or diminishing the subject's opportunities and status in relation to others. Economic risks include payment by subjects for procedures, loss of wages or income, and damage to employability.
Risk of criminal prosecution or civil lawsuit when research methods reveal that the subject has or will engage in conduct for which the subject or others may be criminally or civilly liable.
Loss of Confidentiality
Confidentiality is presumed and must be maintained unless the investigator obtains the express permission of the subject to do otherwise. Risks include invasion of privacy, as well as the social, economic and legal risks outlined above.
Federal regulations define "minimal risk" as follows: "The probability and magnitude of harm or discomfort anticipated in the research are not greater in and of themselves than those ordinarily encountered in daily life or during the performance of routine physical or psychological examinations or tests." In broad terms, a project involves minimal risk if:
- The participant experiences no pain or physical danger;
- The participant experiences no emotional arousal or psychological stress beyond the levels normally to be expected in everyday life;
- The project neither induces nor attempts to induce long-term significant change in the participant's behaviors (including attitudes toward self and others);
- The data would not embarrass or socially disadvantage the participant, were confidentiality to be violated; and
- If the investigator conceals information about the specific purpose of the project, there is no reason to believe the subject would choose not to participate if s/he had known that information initially.
- Office for Human Research Protections
- Canvas Training Course on Protection Human Research Participants
Questions should be directed to current chair of the IRB.
Sheryl Steadman, Ph.D
Dean of Nursing & Health Sciences