When we are conducting a clinical trial on a health condition that you have, we may want to contact you. For this to occur we need to record health information about you.
People who are healthy can also volunteer to be recorded in our Volunteer Database as some clinical trials need participants who have no known health conditions.
This database enables researchers to quickly identify suitable trial participants and will allow clinical trials to be carried out more.
We would like to collect the following information from you.
Directly from you.
All clinical trials have guidelines about who can participate. Criteria may include age, gender, the type and stage of a disease, previous treatment history and other medical conditions.
You can access new research treatments before they are widely available, and your participation also may help others by
contributing to medical research.
Participants are generally asked to come in for regular office visits at an accessible clinical trial site, which may be a doctor’s
office or dedicated clinical trial centre. Some trials require more doctor visits than would be normal for an illness or condition.
Many trials involve a physical examination or medical history review after enrolment. A description of what’s expected of the
participant should be made available before signing the informed consent document.
The information we collect from you will help us decide whether you should be notified about a clinical trial and will enable us to get in touch with you easily. Your decision to provide this information is completely your choice. If you decide not to provide this information it will not affect your ongoing healthcare with your primary healthcare provider.
Under the Privacy Act 2020 you are entitled to request access to the personal information we hold about you. You can request to be removed from the database, view the information held, and change any details at any time. There is no obligation for you
to participate in any of the clinical trials that we contact you about.