Date: May 7, 2015 from 2-3:30pm
This session, facilitated by clinical research experts Judith Hall and Stephanie De Masi, will explore how to develop a clinical research protocol using SPIRIT (Standard Protocol Items: Recommendations for Interventional Trials) and CONSORT (Consolidated Standards of Reporting Trials) guidelines and tailoring the protocol to your audience, a review of the PRagmatic-Explanatory Continuum Indicator Summary (PRECIS) tool, tips for using PICOT to help frame your question, information on how to register your protocol, as well as an example of a protocol developed through the HUB.
This workshop is provided by the Applied Health Research Centre at the HUB Health Research Solutions of St. Michael’s Hospital and is open to staff, students, faculty, researchers and physicians at St. Michael’s and the University of Toronto.
Facilitators: Judith Hall, Manager, Clinical Trials Unit; Stephanie De Masi, Clinical Trials Unit.
Registration: Contact Sarah Grant Alvarado firstname.lastname@example.org . Attendance is limited to 35 participants.