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.
ASPREE Protocol AUS Version # 9 Nov 2014
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 ‘THE 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
