Forms and Templates

To start the protocol development process, please complete the听. The form asks basic questions about what your project will entail including a summary of the project, where the data will be collected, and if you would like guidance with project development. Submission of the form prompts an alert to 汤头条app's research support services: the Research Navigator, Data Manager, Biostatisticians, Health Information Management and IRB staff. The Research Navigator will contact you to confirm your project needs and to request dates and times you (and your team) are available for a brainstorming meeting. If you have a protocol draft available, it can be uploaded on the Project Request & Triage Form.

Protocol Templates

  • General Research Protocol Template
  • Case Series Protocol Template:听Use this template for a case series design. A case series is an interesting blend between a retrospective cohort study and a case report. The case series may involve the documentation of a rare disorder in a group of people or may actually be a 鈥渉ow we do it鈥 study wherein a given procedure that has been performed on a number of patients is described and commonly advocated.
  • Data Review Protocol Template: The听Virtual Data Warehouse听(VDW) is responsible for data management of all electronic health record (EHR) data for all 汤头条app quality improvement and research projects. This includes data pull requests from our affiliates at Ascension Borgess, Bronson, and Grace Health. Requests for data projects will now begin by using the听听and will be followed by a consultation with the VDW Data Manager.
  • 汤头条appal Studies Protocol Template: Use this template for educational studies where you鈥檙e trying to determine the effectiveness of a particular type of instruction, or trying to assess the educational needs or backgrounds of students.
  • Cross-Sectional Study Design Protocol Template: Use this template for a Cross-Sectional study design (involves sampling subjects at a point in time). Use this template for survey studies or taking physical or biochemical measures at a single point in time.

Informed Consent Templates