Nursing Student
Research/Practicum/Project Policy
      All requests for nursing students (BSN, MSN,  DNP, PhD) who are seeking to do original research (OR), a DNP project such as,  but not limited to quality improvement (QI) or evidence based practice (EBP),  or a research practicum experience must be submitted to the clinical placement  coordinator from the student’s school through the Centralized Clinical  Placement System (CCP).  A current  contract between the school and MGH must be in place prior to the start of the  practicum or project/research study. Of note: if a school does not have a  contract, they should send a request with the following information to the Institute  for Patient Care at PCSIPC@partners.org, Attention: Clinical Placement Coordinators.  Please allow one week for us to respond.
      
        - The student’s faculty member must oversee and grade the student’s  practicum or project/research study.
- The Institute for  Patient Care’s Professional Development Manager or Project Manager for the  Clinical Affiliation Program will send the request to the MGH nursing community  to determine if there is an MGH nurse who is willing to serve as the student’s  preceptor for the practicum or project/study.  
- The request must be made at least 8 weeks prior  to the anticipated start date. 
- Student  placements are not guaranteed.
For students wishing to  do a research practicum experience at MGH, the following process applies. 
      
        - The faculty member and student must review the skills sought for  practicum and submit a list of the skills the student is seeking  during this experience into the CCP along with  the course syllabus.  
- The faculty member and student using the skills list, must discuss the  goals of the practicum with the MGH preceptor. 
- It is the faculty member’s  responsibility with input from the MGH  preceptor to grade the student.  
For students wishing to conduct original research or quality improvement, the following applies: 
      
        Prior to the start date  at MGH, each student must complete CITI certification at http://www.citiprogram.org.  The CITI program required by the school may be different  than the one required at MGH, which at minimum requires the Good Clinical  Practice module be complete.
      
      
        - MGH employees are strongly encouraged       to discuss their project with their unit leadership as a first step.
- It       is the expectation that students will work with their faculty member to       establish their research question, approach to the problem and plan for evaluation       or data analysis.
- In addition, a proposal with       the following information must also be included in the application.
          - Title of the quality        improvement project or original research study
- The research question and/or        specific aims of the study or performance improvement goal
- Brief overview of the method/approach 
- Subject population of interest
- Data analysis or performance        improvement evaluation plan
- Signature of faculty member        overseeing the DNP project or PhD dissertation 
- Signature of MGH preceptor
- Signature of MGH unit        leadership member approving that the project can be conducted on their        unit
- The faculty member, student        and MGH preceptor should each retain a copy of this information
- At the end of the experience        and as applicable, it is the        faculty member’s responsibility with input from the MGH preceptor to        grade the student.
        
          - DNP student projects must be human subjects exempt        from IRB as described here:
New “Not Human Subject Research (NHSR)” Application (Formerly Quality Improvement  Checklist)  The new REDCap application replaces the paper  version of the NHSR form and the QI Checklist previously used.
      
        - If you would like to  seek an official determination that a project is “not human subjects research,”  click on the link above to submit a request to the IRB (Not Human Subject Research Determination (partners.org)).   The IRB will quickly review your  project description and provide you either a written confirmation that your  project is “Not Human Subjects Research (NHSR)” or direct you to submit a full  IRB application if you are conducting human subject research
 
      
        - Activities that do not  meet the definition of human subject research may qualify for a NHSR  designation. Some examples include: 
- Quality  improvement/assurance projects or program evaluations
- Use deidentified data or  specimens with no intent to re-identify subjects
- Use of cadaveric  materials or data.
        
          - It is not acceptable for        schools to submit to -MGB IRB for a learning experience if they meet the        standard of a QI project..
IRB: 
      
        - For OR and as part of a PhD program ONLY, once the MGH preceptor  agrees to be the onsite responsible investigator, the following applies.
        
          - All original research conducted        at MGH must be approved by MGB IRB. 
- It is the faculty member’s        responsibility to oversee all IRB approval. 
- Some schools have a        partnership agreement with MGB IRB. The faculty member and student must        check with the school’s IRB to determine if this is the case and the        process to follow. For example, in some cases the student will need to go        through the school’s IRB first then once approved, submit a cede review        application for approval to the MGB IRB. A full MGB IRB review may still        be required. In other cases, the opposite is true and MGB IRB approval is        required first; then the MGB IRB approval is submitted to the school, 
- In either case, the IRB application        must be prepared by the faculty and student. The MGH preceptor who serves        as the site responsible investigator will sign off and submit the        application. 
- Revisions to the application and the        completion of continuing reviews are the responsibility of the faculty        member and student and signed off by the MGH site responsible        investigator.