• Please be sure to click save before exiting the site OR clicking on any of the hyperlinks within this form as doing so will take you out of the form and progress will be lost.

  • Please indicate if this is your initial or revised submission. Note, if this is a revision, please be sure all revisions have been made in all necessary attachments and all revisions highlighted throughout.
  • Research Ethics Committee (REC) Cover Page

  • Training Requirement:

    All individuals involved in human subjects research are required to complete training in the protection of human research participants.
  • Completion of training must occur prior to the final approval of this research project proposal. A web-based training program through the Collaborative Institutional Training Initiative (CITI) can be accessed at https://about.citiprogram.org/en/homepage/ 

    All investigators must submit a certificate of completion with this research project proposal.

    Note: CITI training must be renewed every three (3) years.

    Click here to upload CITI training certificates of completion. Note, if you have already submitted your CITI certificate you do not need to resubmit here. By clicking to upload your certificate here, you will be redirected to a different form and will need to use the back button in your browser to get back to the first page of this form. 

  • By Checking YES, you verify that ALL listed investigators have completed CITI training and submitted certification of completion.*
  • Some projects involve multiple components. Please select all that apply to the proposed research.*
  • If you will be doing records / chart review as any part of your research, you will also need to complete the application to conduct records-based research https://form.jotform.com/223033741588053 

    If you are doing only records review then you only need to fill out the records-based research application and do not need to proceed with this form. 

    If you are doing records review in addition to other data collection then you will need to complete this form and the records-based application form. 

  • INVESTIGATOR(S) INFORMATION:

  • Investigator Role*
  • Does the PI / Faculty advisor have a conflict of interest (COI) to disclose?*
  • Format: (000) 000-0000.
  • Format: (000) 000-0000.
  • Investigator Role
  • Does this investigator have a conflict of interest (COI) to disclose?
  • Format: (000) 000-0000.
  • Format: (000) 000-0000.
  • Do any (other) investigators have a conflict of interest (COI) to disclose?
    • Click here to enter additional investigator information 
    • Investigator Role
    • Format: (000) 000-0000.
    • Format: (000) 000-0000.
    • Investigator Role
    • Format: (000) 000-0000.
    • Format: (000) 000-0000.
    • Collaborating Investigator(s) and Affiliation(s):

      Please use the spaces below to enter the names and affiliations of any collaborating investigators.
    • Browse Files
      Drag and drop files here
      Choose a file
      Cancelof
  • This section will help determine the appropriate level of review needed for this proposal.

  • REC review is required whenever you are conducting research (a systematic investigation designed to contribute generalizeable knowledge) involving human subjects. The questions below will help deterime if your project qualifies as human subjects research and whether or not it meets criterion for exempt status. 

  • Is the purpose of your research solely to improve processes internally at a specific organization?*
  • Is the activity a systematic investigation designed to develop or contribute to generalizable knowledge (I.e. is it research)?*
  • Does the research involve a LIVING individual about whom you will (select ALL that apply): [Note, use of an anonymous survey IS an interaction and environmental modification IS an intervention]-the first option applies to most*
  • According to your selection above, your research may qualify for exempt status, if certain conditions are met. Please be sure to review the decision charts linked on page 7 of this form prior to selecting the level of review needed for this proposal. 

    Click here to review exempt categories on the REC website. 

  • ESTIMATED PROJECT DURATION:

    Please be sure your start date reflects time needed for review and revision of the proposal.
  • Estimated Start Date (please allow ample time for REC review)*
     - -
    2 digit month, 2 digit day, 4 digit year
  • End Date*
     - -
    2 digit month, 2 digit day, 4 digit year
  • FUNDING INFORMATION (If Applicable):
  • RESEARCH PROJECT SITE(S) Note, if data collection is online please indicate that in lieu of site along with the survey platform used. For any fields that do not apply enter NA:*
  • Browse Files
    Drag and drop files here
    Choose a file
    Cancelof
  • TARTGETED PARTICIPANT POOL:*
  • Targeted participants are considered potentially vulnerable to coercion or undue influence and/or may require additional protections if categorized as any of the following vulnerable populations (mark each box that applies).*
  • LEVEL OF REVIEW

    Please use the following section to indicate the appropriate level of review.
  • EXEMPT: This research project is eligible for exempt review because it meets at least one of the following criteria:

    1. Research conducted in established or commonly accepted educational settings, involving normal educational practices.
    2. Research involving the use of educational tests, survey procedures, interview procedures, or observation of public behavior, EXCEPT when participants can be identified and such disclosure results in risk.
    3. Research involving benign behavioral interventions (i.e., brief in duration, harmless, painless, not physically invasive, no significant adverse lasting impact, and not offensive or embarrassing to participant) in combination with the collection of information, EXCEPT when participants can be identified and such disclosure results in risk.
    4. Secondary research for which consent is not required (e.g., participants identity cannot be readily ascertained, identifiable information is publically available, identifiable information was originally collected for non-research purposes, or collection and analysis of identifiable information are for the purposes of “health care operations,” “research,” or “public health activities and purposes).Taste and food quality evaluation and consumer acceptance studies.
    5. Research and demonstration projects conducted or supported by a federal department or agency that are designed to study, evaluate, improve, or otherwise examine public benefit or service programs.
    6. Taste and food quality evaluation of consumer acceptance studies.
    7. Storage or maintenance for secondary research for which broad consent is required.
    8. Secondary research for which broad consent is required.

    EXPEDITED: This research project is eligible for expedited review because the research activities present no more than minimal risk to human subjects and it meets at least one of the following criteria: 

    1. Clinical study of drug and medical devices only when an investigational new drug or device exemption application is not required and when the medical device is approved for marketing and being used in according to the approved labeling.
    2. Collection of blood samples by finger stick, heel stick, ear stick, or venipuncture that follows approved practice guidelines.
    3. Prospective collection of biological specimens for research purposes by noninvasive means.
    4. Collection of data through noninvasive procedures routinely employed in clinical practice, excluding procedures involving x-rays or microwaves.
    5. Research inolving materials that have been or will be collected solely for non-research purposes.
    6. Collection of data from voice, video, digital, or image recordings made for research purposes.
    7. Research on individual or group characteristics or behavior, or research employing survey, interview, oral history, focus group, program evaluation, human factors evaluation, or quality assurance methodologies.
    8. Continuing review of research previously approved by the REC or IRB where the research is permanently closed to the enrollment of new subjects, all subjects have completed all research-related interventions, and the research remains active only for long-term follow-up of subjects; or where no subjects have been enrolled and no additional risks have been identified; or where the remaining research activities are limited to data analysis.
    9. Continuing review of research involving no greater than minimal risk and no additional risks have been identified.

    FULL: This research project requires a full board review because it is not eligible for an exempt or expedited review (based on the criteria listed above) and/or it meets at least one of the following criteria: 

    1. Research activities involves greater than minimal risk to participants.
    2. Involvement of intentional deception, such that misleading or untruthful information will be provided to participants.
    3. Inclusion of participants of special consideration (e.g., vulnerable populations).
    4. Use of procedures that are considered intrusive, stressful, or potentially traumatic.
  • Please refer to these ORHP decision charts as needed for more information regarding potential exemptions. These can also be found on the REC website, www.rec.spalding.edu 

  • RESEARCH PROJECT PROPOSAL OUTLINE:

    Please be sure that all necessary components are included in your proposal. Note that some components (i.e. CITI training certificates, site permission letter(s), and consent document(s)) have specific places to be uploaded within this form. All other appendices should be attached as separate files in the space provided below. Proposals missing components and / or associated appendices will not be reviewed. Do NOT submit a thesis, dissertation or capstone proposal, grant application, etc. This proposal is specific for the human subjects research component of those proposals.
  • Please mark each box to indicate you have included each section in your proposal and reviewed it for completion. The proposal will not be reviewed unless ALL of the components are provided. Note, proposals lacking details / information in any of the sections noted below may not be reviewed until the information is received or may be denied due to a lack of sufficient information. Please review each of the following sections carefully to be sure you have provided sufficient information for the committee to clearly understand and make a decision about the proposed research.*
  • Click here to access form templates to be sure the University approved template is followed.

  • Will you be employing surveys or other questionnaires as part of this research?*
  • If utilizing surveys / questionnaires, will you be using the University QuestionPro account?
  • If online survey is the ONLY method of data collection to be used, please select the option which best explains how consent will be documented.
  • Browse Files
    Drag and drop files here
    Choose a file
    Cancelof
  • Browse Files
    Drag and drop files here
    Choose a file
    Cancelof
  • Browse Files
    Drag and drop files here
    Choose a file
    Cancelof
  • Browse Files
    Drag and drop files here
    Choose a file
    Cancelof
  • This page is for uploading revised documents ONLY. 

    Please use the following fields to upload your revised documents. Be sure to include a separate file noting your response to each of the reviewer's comments. 

  • Browse Files
    Drag and drop files here
    Choose a file
    Cancelof
  • Browse Files
    Drag and drop files here
    Choose a file
    Cancelof
  • Browse Files
    Drag and drop files here
    Choose a file
    Cancelof
  • CERTIFICATION / SIGNATURE PAGE

    Proposals will NOT be reviewed without ALL necessary signatures. Faculty advisors must review student proposals PRIOR to submitting this form.
  • Please read each statement before checking:*
  • FOR FACULTY ADVISOR / PRINCIPAL INVESTIGATOR ONLY. By signing below I certify that:
  • Date Signed
     - -
    2 digit month, 2 digit day, 4 digit year
  • Check the appropriate box to confirm your submission as the PI on this project--choose only 1 option--
  • FOR STUDENT or Other Co-Investigators ONLY. By signing below I certify that (if you are unable to select all boxes then please do not submit the form at this time):
  • Date Signed
     - -
    2 digit month, 2 digit day, 4 digit year
  • If you would like to use the separate signature page to attach signatures instead of soliciting via the jotform please upload that below.

  • Browse Files
    Drag and drop files here
    Choose a file
    Cancelof
  • This following section is for signatures of any additional investigators.

    Note that all investigators must sign the proposal.
  • For REC Use Only. DO NOT FILL BELOW THIS LINE

  • Type of review conducted:
  • Approval recommended?
  • Is additional Spalding administration approval needed?
  • Browse Files
    Drag and drop files here
    Choose a file
    Cancelof
  • Date
     - -
    2 digit month, 2 digit day, 4 digit year
  • Should be Empty: