THE ASPREE PROTOCOL
A study protocol is the ‘bible’ for a clinical trial which must be approved by a Human Research Ethics Committee (HRECs) before a study can legally commence in Australia. The ASPREE Study Protocol documents the background to the study, the trial design, objectives, hypothesis, endpoints, patient well-being, study visit measurements, analysis and adherence to ethical regulatory and administrative considerations.
THE ASPREE STUDY BROCHURE
Download the ASPREE Information brochure for general information about the trial or ring 1800 728 745 to order a copy
EDITIONS OF THE ASPREE PARTICIPANT NEWSLETTERS ‘ABOUT A TABLET’
This biannual publication helps keep participants and the general community up to date on all things ASPREE – from study progress through to news stories, reminders and snippets. All submissions and suggestions are welcome! Send through your suggestions to aspree@monash.edu
