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Human Research Ethics: Issues and Procedures

Human Research Ethics: Issues and Procedures. Dr . Constance Jones Chair, Committee for the Protection of Human Subjects. Overview. Why? Who and What is Covered? Levels of Risk CSUF Procedures for Obtaining Human Subjects Approval CSUF Paperwork for Obtaining Human Subjects Approval.

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Human Research Ethics: Issues and Procedures

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  1. Human Research Ethics: Issues and Procedures Dr. Constance Jones Chair, Committee for the Protection of Human Subjects

  2. Overview • Why? • Who and What is Covered? • Levels of Risk • CSUF Procedures for Obtaining Human Subjects Approval • CSUF Paperwork for Obtaining Human Subjects Approval

  3. Overview • Why? • Who and What is Covered? • Levels of Risk • CSUF Procedures for Obtaining Human Subjects Approval • CSUF Paperwork for Obtaining Human Subjects Approval

  4. Why? • All agencies receiving federal funds (all public universities) are required to have an Institutional Review Board • Protection of: • Research participants • Researcher • University

  5. Overview • Why? • Who and What is Covered? • Levels of Risk • CSUF Procedures for Obtaining Human Subjects Approval • CSUF Paperwork for Obtaining Human Subjects Approval

  6. Committee for the Protection of Human Subjects • Covers research done with human subjects <by people at CSUF> • What is research? • What are human subjects?

  7. Research is • Any systematic investigation or collection of data intended for scientific presentation or publication • Researchers may be undergraduate students, graduate students (projects or theses), faculty, staff, administrators

  8. Research is not • Data collected for classroom evaluation, illustrative purposes, or educational purposes

  9. Human Subjects Research can involve: • Contact with humans via telephone, mail (paper or electronic), or in-person interaction • Study of records of human behaviors or attitudes (e.g., case files, police records, hospital records) • Study of specimens collected from humans (e.g., blood, urine)

  10. Overview • Why? • Who and What is Covered? • Levels of Risk • CSUF Procedures for Obtaining Human Subjects Approval • CSUF Paperwork for Obtaining Human Subjects Approval

  11. Risk Categories • No risk research • Minimal risk research • At risk research <risk = equivalent to daily life>

  12. No Risk Research • Study of existing anonymous data • Study of existing documents • Study of publicly observable, legal behavior

  13. Minimal Risk Research • Study of “normal adults’” attitudes opinions, cognitions, personality, etc. • Study of “normal adults’” moderate exercise • Study of “normal adults’” biological specimens

  14. At Risk Research • Study involving possibility of physical or psychological harm • Study involving collection of reports of illegal / embarrassing behavior • Study using deception and debriefing

  15. At Risk Research • Study of protected populations • Those younger than 18 years old • Those with psychological, cognitive, and/or physical impairments • Incarcerated individuals • Pregnant women

  16. Overview • Why? • Who and What is Covered? • Levels of Risk • CSUF Procedures for Obtaining Human Subjects Approval • CSUF Paperwork for Obtaining Human Subjects Approval

  17. Levels of Review • Departmental Chair • Departmental Committee • University Committee

  18. No Risk Research • Unfunded: • Memo to Departmental Chair • Funded: • Departmental Committee, then University Committee (Expedited)

  19. Minimal Risk Research • Unfunded: • Departmental Committee • Funded: • Departmental Committee, then University Committee (Expedited)

  20. At Risk Research • Unfunded: • Departmental Committee, then University Committee • Funded: • Departmental Committee, then University Committee (Full)

  21. Overview • Why? • Who and What is Covered? • Levels of Risk • CSUF Procedures for Obtaining Human Subjects Approval • CSUF Paperwork for Obtaining Human Subjects Approval

  22. CPHS Webpage • Checklists • Example memos • Example Informed Consent Forms • Training modules

  23. Paperwork / Timing Problems • No departmental review • No training certificate • Missing instruments • Missing informed consent forms • Premature submission of grants

  24. Proposal Problems • Lack of clarity in terms of: • Who will be studied • How they will be studied • When they will be studied • Context of study • Minimization of risk • Incorrect classification • Too brief consideration and/or description of risk

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