Welcome to CYCLE!
What You Will Need For Site Start-Up:
Most recent Clinical Trials Ontario approved protocol (Aug-03-2022).
Sample Informed Consent form based on Clinical Trials Ontario Template.
Data Monitoring Committee Charter draft (CTO approved).
Script for obtaining telephone consent from SDMs (CTO-approved).
Budgets and Contracts
Please contact CYCLE Methods Centre for site specific information and documents.
Link to Research Coordinator Page. Bundle of all Case Report Forms found at top of page.
Sample training agenda for new CYCLE sites – includes research coordinator, bike, and outcomes assessor training
Documents all CYCLE training personnel. Outlines every team member and their associated roles. To be completed by all site staff.