Important Information Regarding the COVID-19 (Novel Coronavirus) and Human Research

Human Subject Administrative Support

In response to the current Coronavirus circumstances, the Human Research Protections Program (HRPP) at BYU, in consultation with campus administration, has produced the following guidance for investigators conducting research with human participants.

With the adoption of the iRIS system and videoconferencing capabilities, the Institutional Review Board (IRB) will continue to process applications and conduct review processes on campus or remotely as needed. This includes full-board IRB reviews. All deadlines related to the submission and expiration of protocols remain in effect.


Using Ethical Principles to Assess Current Risks

Given the real or perceived risk of exposure to COVID-19, the risk/benefit ratio for research participation must be reassessed by each PI. Ethical principles of research and federal regulations require an acceptable risk/benefit ratio [(45 CFR 46.111(a)(1-2)]. All researchers should develop plans for continued data collection, communication and data management to protect themselves and their participants from COVID-19. Face-to-face studies for which there is little to no prospect for direct benefit to participants may need to pause data collection until such a plan is in place.


Regulations require researchers to ensure prompt reporting to the IRB of proposed changes in research activity in accordance with the terms of the IRB approval until any proposed changes have been reviewed and approved by the IRB, except when necessary to eliminate apparent immediate hazards to the subject (45 CFR 46.108(3)(iii). Therefore, changes from face-to-face to remote data collection may be implemented immediately without IRB approval. All other prospective changes must be submitted, reviewed and approved by the IRB. Please submit a modification form in iRIS.


Researchers engaging in social behavioral data collection with populations at higher risk of COVID-19 or in settings that put the study team at higher risk (e.g., nursing homes, homeless shelters, schools) are responsible to create plans for ensuring that they are aware of COVID-19 cases in their data collection settings and for following recommended guidelines for reducing exposure and, if prudent, pausing the studies. Study teams need to have plans for regular communication to ensure everyone is operating under the procedures recommended by the University. Researchers should conform to the Center of Disease Control guidelines when face to face contact cannot be avoided.

If research participants will have in-person interactions with researchers or other study participants, all study teams should immediately implement procedures to screen research participants for potential infectious risk prior to any interaction and incorporate mandatory screening prior to scheduled study visits. The incorporation of this screening procedure does NOT require IRB approval.

Guidelines for reducing exposure:

Develop Contingency Plans:

Study teams should proactively prepare contingency plans for their active research protocols. These changes will require IRB approval prior to implementation. Consider whether disruption of a research protocol will impact the safety of your research participants, and how you can manage that disruption.


Specific examples could include:

Protecting the safety of research participants and study personnel is everyone’s responsibility. Please contact the HRPP at 801-422-1461 if you have any questions.