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- Is the research conducted in a standard educational setting using normal teaching practices or based solely on anonymous, publicly available data?*
- Does the study involve only adults (18 years or older) who are not part of a vulnerable or protected population?*
- Does the study avoid sensitive or personal topics (e.g., health status, behavior, cognition, identity, cultural beliefs, religion or psychological condition)?*
- Does the study avoid collecting any identifiable information, directly or indirectly?*
- Will interviews, surveys, or interactions be audio or video recorded?*
- Does the study use in-depth qualitative methods, such as open-ended interviews, focus groups, oralhistories, or narrative analysis?*
- Will the data be stored forfuture research use or analyzed beyond basic descriptive purposes?*
- Does the study involve noninvasive data collection or biological specimen collection (e.g., saliva, cheek swab, height, weight, blood pressure)?*
- Does the study involve retrospective or prospective chart reviews?*
- Are any vulnerable populations involved, such as children, prisoners, mentally ill individuals, or those with impaired decision-making capacity?*
- Does the study involve minor modifications to a previously approved IRB study?*
- Does the study involve more than minimal risk (physical, psychological, social, legal, or financial)?*
- Are the procedures intrusive, stressful, or potentially traumatic for participants?*
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- Please select the medical field of your research proposal*
- What is the design of the study you are conducting?*
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