IRB: Federal changes to reduce burden for human participant researchers to take effect January 21, 2019
The Human Research Protection Program (HRPP) has been established to support researchers whose work involves human participants.
The Scholarly Integrity and Research Compliance division of the Office of the Vice President for Research and Innovation (OVPRI) is implementing changes to comply with new federal Institutional Review Board (IRB) regulations. A primary goal of the revised regulations is to reduce the regulatory burden on researchers, and these changes will benefit researchers at Virginia Tech. The revisions to the Common Rule for the protection of human research participants go into effect on January 21, 2019.
Some of the key regulatory changes include:
- Abbreviated reviews for studies with less risk
- A single IRB review for multi-site studies
- Improvements in what is required in consent forms to help participants make informed decisions about joining a study
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Under the new rule, some studies may receive only a brief review of certain protections instead of a full review by the IRB. In addition, some minimal-risk studies will no longer require annual review.
It is important to note that even without an annual review, researchers are still required to keep the HRPP office up-to-date on any concerns or events to ensure that research subjects are protected.
Although NIH-funded multi-site studies have been required to use a single IRB review since 2018, the federal-wide requirement to have a single IRB oversee studies that are conducted at multiple sites does not go into effect until January 2020.
Once implemented, a single IRB will serve as the reviewing board for all sites involved in a multi-site study. This will reduce multi-site review delays that have occurred in the past when the different sites’ IRBs attempted to reconcile the various, sometimes contradictory, requirements.
Researchers will have the opportunity to work with HRPP Protocol Coordinators. To support the growing research environment, Virginia Tech is hiring several new HRPP Protocol Coordinators to augment the existing IRB support staff An HRPP coordinator will be assigned to handle each study throughout the lifecycle of the protocol—from preparation for IRB submission through study closure. Coordinators will be available to answer questions, direct researchers to resources, and provide updates on where the researcher’s study is in the process.
HRPP is also enhancing the training of and strengthening its connection with Departmental Human Subjects Advisors. This corps of advisors comprises faculty and staff with expertise in their unit’s human subjects research portfolio and additional expertise in research ethics and IRB regulations. They serve as a bridge between faculty, HRPP, and the IRB and can assist fellow faculty with research ethics and IRB-related questions. In many instances, they can provide the initial determination of whether or not a protocol must undergo IRB review.
In preparation for the upcoming changes and to improve the IRB process overall, the Division of Scholarly Integrity & Research Compliance created a Human Research Protections Program (HRPP) to support researchers whose work involves human participants. HRPP has improved education and training to bring researcher training to industry standard by January 21, 2019.
Virginia Tech will now use the same training required at other universities and federal research institutions. The Collaborative Institutional Training Initiative (CITI) training is transferrable and meets requirements for collaborative or multi-site studies. If a researcher has previously taken CITI human protections training either at Virginia Tech or at another institution, they can affiliate with Virginia Tech through their CITI account to transfer completed courses without retaking them.
HRPP enlisted researchers and stakeholders from across campus to review the updated Human Research Protection Training Requirements Standard Operating Procedure. Input from Professors Kevin Carlson, Rosemary Blieszner, Karen Roberto, Marie Paretti, and Kathy Hosig provided helpful insights from the user perspective.
CITI training is available online and is self-paced to meet the researcher’s schedule. It provides information on both the regulatory requirements and the ethical context necessary to understand human research protections. “We expect that researchers who have completed the training will be able to write improved protocols and receive faster approval,” said Suzie Lee, IRB Chair.
CITI human subjects research training will be available beginning January 21, 2019. The new training will be required for all initial researcher training starting on that date.
To comply with the revised regulations, HRPP is updating its standard operating procedures with a nationally vetted toolkit and accompanying training from Huron Consulting. Vice President for Research and Innovation Theresa Mayer said “The toolkit will include additional guidance, researcher checklists, and other job aids to ensure that we put the right tools into the hands of researchers.” These additional tools walk researchers through the process and help them to understand how the regulatory changes affect their studies. These tools will be a part of the updated HRPP website coming soon.
The Virginia Tech HRPP is also continuing to integrate its internal processes with an external IRB to ensure that there are subject matter experts available to review protocols in a timely manner. Phase 3 of the Protocol Management system, which reduced the number of steps required to use the external IRB, was released on October 22, 2018 and phase 4 planning and development is underway.
One of the most substantial changes to the federal regulations addresses research participant consent. The change requires that consent forms outline up front the key information that potential participants need to make the decision about whether to join the study. This information includes potential risks and benefits of the research and the impact these might have on the participant.
To help potential participants find and understand this crucial information, informed consent documents will now open with a summary, written at a level consistent with average reading levels of the study population. In addition, the consent documents will explain to potential participants whether the results of the research will be shared with them at the end of the study.