Common Mistakes to Avoid
If you have questions at any point in the submission or approval process, contact the HSP Office.
If you have questions at any point in the submission or approval process, contact the HSP Office.
The Human Subjects Research Office is pleased to announce that Ginni Strehle, member of the Infant Learning Project lab, has been selected as the recipient of the Spring 2022 IRB HIVE Award! Ms. Strehle is currently an undergraduate student who will be graduating with her B.S. in Psychology this semester, is a fast-track student …read more
Any active study is subject to a post-approval review via our post-monitoring program (PMP). The purpose of the PMP is to assess the research activities conducted under the University’s Federal Wide Assurance Agreement with the Office of Human Research Protections (OHRP). This program assures human subject safety in research, provides education to research professionals, and …read more
The IRB requires PI to promptly report (within 5 days) a summary of reportable events (including unanticipated problems and deviations) using the Reportable Events Report in Cayuse IRB. Examples of events that require reporting to the IRB include but are not limited to the following: Information that indicates a new or increased risk, or a new …read more
Office for Human Research Protections (OHRP) Office for Human Research Protections (OHRP) Educational Videos Research Use of Human Biological Specimens and Other Private Information Reviewing and Reporting Unanticipated Problems and Adverse Events Investigator Responsibilities FAQs (OHRP) Research with Children FAQs (OHRP) Prisoner Research FAQs (OHRP) International Compilation of Human Research Standards Compilation of European GDPR …read more
Certificates of Confidentiality (CoC) are issued by the National Institutes of Health (NIH) to protect identifiable, sensitive information participant information collected in the course of a research study. Identifiable, sensitive information is defined as information that is about an individual and that is gathered or used during the course of research where the following may …read more
Modifications All changes to an approved research protocol (including changes to consent forms, recruitment scripts / flyers, study measures, personnel, protocol procedures / activities, etc.) must be reviewed and approved prior to the changes taking effect, except when necessary to eliminate immediate hazards to subjects. Modifications must be submitted through Cayuse. All changes must be …read more
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Use of deception and incomplete disclosure generally goes against a basic principle of human subjects research: to treat individuals as autonomous agents by disclosing complete and truthful information about a study. However, the IRB recognizes it can be a useful tool, especially in behavioral and social research. The information below provides guidance on the appropriate …read more
In this Comet Corner session, the Office of Research and Innovation hosted a Women’s History Month event, highlighting the work of UTD Geosciences alum Dr. Allie Kennedy Thurmond, B.S. ’97, M.S. ’02, Ph.D ’07, Head of Exploration Assets in the US Gulf of Mexico. Focusing on her work and diversity in STEM education, this virtual …read more