The IRB's mission is to protect human subjects from any harm that could befall them by participating in research. The CORONAVIRUS pandemic provides additional risks to research subjects beyond those they usually encounter. Before submitting your IRB application, please read the attached document.
Information Regarding Submission of IRB Protocols
Projects that involve humans as research participants are submitted for review and approval by the University's Institutional Review Board (IRB) through a cloud-based software- Cayuse IRB.
With Cayuse IRB, the Institutional Review Board (IRB) submission process is streamlined, providing greater access to your IRB records.
First time users should request a Cayuse user ID. Send an email to firstname.lastname@example.org and provide your St. John’s email address and your academic department.
Researchers that have their user ID can access Cayuse IRB through the following link: https://stjohns.cayuse424.com/
IMPORTANT: The federal regulations for human subjects research have been revised as of January 21, 2019. Major changes include (but not limited to):
1. Changes to informed consent
2. Additions and revisions to exempt categories of research
3. Revised definitions and new terms
Projects proposed by faculty, students, and administrators involving the use of humans or animals as participants in research must be submitted for special institutional review and approval. Generally, funding sponsors and agencies expect that this review process will be completed - and institutional approval obtained - prior to submission of a grant proposal. These reviews are intended to minimize discomforts and/or risks to the participants and to assure that researchers comply with Federal regulations. Please be advised that all individuals submitting applications or interacting with human participants must obtain a certification demonstrating their knowledge of research ethics. Download the information on the certification exam below.
More information regarding these changes can be found here.
Projects that involve humans as research participants should be submitted for review and approval by the University's Institutional Review Board (IRB). Complete information regarding the University's policies and procedures on the use of humans as subjects can be obtained from the following documents:
The US government's Office for Human Research Protections has a special web page that details concerns and frequently asked questions about research with children. If you are doing research with children, please consult this web page: Research with Children FAQ’s
Please see the University's Institutional Animal Care and Use Committee for more information on animal use.
Dr. Raymond DiGiuseppe, Ph.D.
Marie Nitopi, Ed.D.
Jared E. Littman, M.P.A., ’22 Ph.D.
Director, Office of Grants and Sponsored Research
Manager, Institutional Review Board (IRB)
Newman Hall, Room 106
The University’s IRB, or Institutional Review Board, is a federally mandated committee of faculty, administrators, medical doctors and community representatives, which is charged to review and approve all research protocols involving humans as participants and created by anyone affiliated with St. John’s. The IRB exercises its responsibility to protect the rights and welfare of human participants in various categories of research in any way related to the institution. The IRB has authority over approval, modification, ongoing review, verification of changes or suspension or termination of approval of research involving human participants, including St. John’s students.
What is the primary function of the Institutional Review Board (IRB)?
The major function of the IRB at St. John’s University is to provide protection for the rights and welfare of any human participants involved in research. The Board reviews in advance all research proposals from within the University that proposes to involve people as participants. The IRB is guided by ethical principles laid out in the Belmont Report with specific reference to 45 CFR 46, and by the principle of respect for human persons taught by the Catholic Church. The St. John’s University Senate has also created specific conditions for recruiting St. John’s students as research participants.
Who should be aware of the IRB process?
All faculty, students and administrators involved in research connected to St. John’s University should be aware of the IRB procedures and elements of informed consent which must be observed when doing any research that uses people as participants.
What is the Review Process like?
Applications for formal approval of research can be obtained on the St. John’s University website. This application is to be filled out and sent to the IRB in Newman Hall 108. All applications must have the appropriate signatures (i.e. Principal Investigator, Faculty Supervisor, Department Chair and Dean) before the review process can begin. Researchers can refer to the “Guidelines for Protocol Submission” for assistance in the application process.
St. John’s University’s IRB generally holds its monthly Board meetings on the first Monday of each month. After an initial review, the Chair or individual members of the IRB can approve through expedited review or take the protocol to the monthly Board meeting to discuss the application with the other members of the Board. The Board members discuss and vote on approval of the protocol. An application can also be found exempt from review under certain specific conditions, but only the IRB can make this determination of exemption. If the Board does not approve the application, the applicant is informed of the revisions that are needed in order for the application to be approved.
The St. John’s University IRB also now requires all individuals to be certified in working with human participants. Certification can be obtained online through Canvas Course here.
At times, the University receives informal inquires from outside sources about doing surveys with our students. Any such request received by anyone should be cleared with the IRB. These informal inquires can be directed to the Chair of the IRB, Dr. Raymond DiGiuseppe at 718-990-1955.
Attention to issues of informed consent and human dignity, which the procedures of the IRB are intended to stimulate and encourage, is an important aspect of the St. John’s mission to educate for ethically empowered decision-making. The members of the IRB want to work with every sector of the St. John’s community to promote that mission.
Raymond DiGiuseppe, Ph.D., IRB Chair
Mabel Abraham, Ph.D.
Robert Eschenauer, Ph.D.
John Fitzgerald, Ph.D.
Mary Noe, Esq.
Samuel Ortiz, Ph.D.
Sandra Reznik, Ph.D.
Jay Zimmerman, Ph.D.
IRB Coordinator: Marie Nitopi, Ed.D.
From the Code of Federal Regulations 45 CFR 46: 116 and 117
Nine Basic Elements of Informed Consent
Additional Elements on Informed Consent Forms When Appropriate
Sample Consent Forms
When must I submit a Request for Approval of Human Participants Research Application Form to St. John’s University’s Institutional Review Board (IRB)?
The principal function of the IRB is to protect individuals who volunteer to participate as human participants in research. The federal regulations (i.e. Title 45 CFR Part 46) define research as: “ a systematic investigation, including research development, testing and evaluation, designed to develop or contribute to generalizable knowledge” (§46.102, D). Thus, any project that involves human participants, is carried out at St. John’s University, and meets the above definition is considered research. The regulations define human participants as “a living individual about whom an investigator (whether professional or student) conducting research obtains (1) data through intervention or interaction with the individual, or (2) identifiable private information” (§46.102, F). There are, however, recurring questions about what exactly constitutes reviewable research or research-related activities.
Over the years, questions have arisen as to whether certain student’s projects constitute research. For example, in a number of courses (e.g., research methodology) students might be required to carry out “research” projects in which anonymous data from surveys, interviews, or laboratory tasks are collected from class peers or from students outside of class or outside of the University. Because the main purpose of such typically minimal risk projects is to teach students about the process of research and because by their nature they do not lead to generalizable knowledge (that is, they will not be disseminated in a public forum or published), they are NOT considered research and, therefore do not have to undergo IRB review.
On the other hand, in more advanced courses (e.g., Independent Study) student projects are sometimes carried out with the potential intention to present or publish the results of the project. In those cases, IRB review is necessary. Likewise, all master’s thesis and doctoral dissertation research projects that involve human participants must undergo IRB review, since they are research by definition and are considered publications when they are filed with ProQuest (formerly UMI). All such projects must be approved by the IRB before data collection begins. Data that are collected from any type of project prior to or without IRB review, even if such data are preliminary in nature, such as from a pilot study, may not be used later for dissemination (e.g., publication, conference presentation, thesis).
It is also possible that certain student projects that do not constitute research place their participants at some level of risk. For example, a seemingly innocuous survey or interview could conceivably cause a subject considerable amount of stress or embarrassment. Perhaps a student researcher is interested in surveying students for other not uncommon behaviors, such as, under-age drinking or speeding. However, these behaviors are illegal and any breach in confidentiality of such data could conceivably place the subject at some risk, and even neophyte researchers incur some responsibilities when in possession of such knowledge of their peers’ behavior. Such projects can be problematic and therefore the IRB should be consulted before any data are collected. Faculty members are strongly urged to exercise care and judgment in designing such classroom exercises, to incorporate informed consent training into their curricula and to refer individual student projects for IRB review as necessary.
Incomplete or Inadequate Applications
On occasion an IRB application must be returned to the individual because it is either incomplete or so poorly prepared that it cannot be properly evaluated. Therefore, we strongly recommend that faculty carefully review IRB applications (their own as well as those from their students) for accuracy and completeness before submitting them. In addition, everyone should keep in mind that such applications must go through various stages or review and approval (e.g., Department chair, Dean) before they reach the IRB. Thus it pays to carefully plan the research project and craft the application.
Please note: the IRB has begun returning unreviewed protocols which fail to answer the questions posed and refer to an attached methodology section or statement from a thesis or dissertation proposal. The questions must be answered within the protocol form itself. The only attachments required are copies of survey instruments, consent forms, letters of institutional permission (when necessary), correspondence with any other IRB, and the signed pledge of compliance.
Institutional Review Board
Dr. Raymond DiGiuseppe, Chair
Marie Nitopi, Ed.D.
Newman Hall, Room 106
Modeled after CUNY’s policy for student research with human participants.
Institutional Review Board meeting dates for the 2021-2022 academic year are as follows:
September 12, 2021
October 11, 2021
November 8, 2021
December 6, 2021
January 10, 2022
February 7, 2022
March 7, 2022
April 4, 2022
May 2, 2022
June 6, 2022
July 11, 2022
August 1, 2022
IRB applications that require full board review must be submitted by the 15th of the month prior to the meeting date in order to be considered at the following meeting.
Projects involving the use of animals should be submitted to the University's Institutional Animal Care and Use Committee (IACUC), headed by Dr. Louis Trombetta. The University's IACUC will evaluate the number of animals to be used, the selection of species, and the animals' possible exposure to discomfort and pain. Animal use review and approval is generally governed by regulations outlined in the NIH Publication Guide for the Care and Use of Laboratory Animals. More specifically, animal use is governed by the following federal laws: Animal Welfare Act, P.L. 89-544 as amended by P.L. 91-579, 94-279, and 99-198, and the regulations promulgated in CFR, Title 9, Subchapter A, Parts 14.
Separate from the animal use and care review committee is the Animal Care Center. For information regarding day-to-day operations of, or special needs from, the Animal Care Center, contact the Center's Director. The Animal Care Center reports to the Chair of the IRB.
IRB and IACUC approval is necessary for all projects involving humans and vertebrate animals, respectively. IRB and IACUC approval is not limited to projects funded through external grants.
Institutional Animal Care and Use Committee (IACUC)
Dr. Louis Trombetta
Animal Care Center