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CITI Training: Belmont Report Questions and Answers | Latest Version | 2025/2026 | Correct & Verified

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CITI Training: Belmont Report Questions and Answers | Latest Version | 2025/2026 | Correct & Verified What constitutes research misconduct? Fabrication, falsification, or plagiarism in proposing, conducting, or reporting research. What is the difference between minimal risk and more-than-minimal risk research? Minimal risk is no greater than daily life risks, while more-than-minimal risk involves potential harm beyond daily life experiences. How can researchers minimize risk in studies involving sensitive information? Use de-identified data, secure storage, and limit access. What is the purpose of a data use agreement? To specify how data will be shared, stored, and protected between entities. Why should researchers avoid coercion in participant recruitment? To ensure voluntary and informed participation. 2 What is the purpose of continuing IRB review? To monitor ongoing research for compliance and participant safety. How should researchers respond to suspected research misconduct? Report it to the institutional compliance office for investigation. What is an example of a protected health information (PHI) identifier? Names, addresses, social security numbers, or medical record numbers. Why must researchers complete CITI training before beginning research? To demonstrate understanding of ethical standards, regulations, and best practices. What is the purpose of an assent process for minors in research? To allow children to agree to participation appropriate to their age and understanding. How should researchers handle conflicts between study protocols and participant safety? Prioritize participant safety and consult the IRB for guidance. 3 What is the definition of identifiable private information? Data from which participants can be directly or indirectly identified. What is the primary purpose of CITI training for researchers? To ensure knowledge of ethical standards, regulatory requirements, and best practices in research. What is the definition of human subjects research? Research that involves living individuals from whom data is obtained through interaction or identifiable private information. Why is informed consent necessary in research involving human participants? To ensure participants understand the study, risks, benefits, and their rights. What is the role of an Institutional Review Board (IRB)?

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CITI Training: Belmont Report
Questions and Answers | Latest
Version | 2025/2026 | Correct & Verified
What constitutes research misconduct?


✔✔ Fabrication, falsification, or plagiarism in proposing, conducting, or reporting research.




What is the difference between minimal risk and more-than-minimal risk research?


✔✔ Minimal risk is no greater than daily life risks, while more-than-minimal risk involves

potential harm beyond daily life experiences.




How can researchers minimize risk in studies involving sensitive information?


✔✔ Use de-identified data, secure storage, and limit access.




What is the purpose of a data use agreement?


✔✔ To specify how data will be shared, stored, and protected between entities.




Why should researchers avoid coercion in participant recruitment?


✔✔ To ensure voluntary and informed participation.


1

, What is the purpose of continuing IRB review?


✔✔ To monitor ongoing research for compliance and participant safety.




How should researchers respond to suspected research misconduct?


✔✔ Report it to the institutional compliance office for investigation.




What is an example of a protected health information (PHI) identifier?


✔✔ Names, addresses, social security numbers, or medical record numbers.




Why must researchers complete CITI training before beginning research?


✔✔ To demonstrate understanding of ethical standards, regulations, and best practices.




What is the purpose of an assent process for minors in research?


✔✔ To allow children to agree to participation appropriate to their age and understanding.




How should researchers handle conflicts between study protocols and participant safety?


✔✔ Prioritize participant safety and consult the IRB for guidance.

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