Participate in the ADNeT Registry

FAQs for
the General Public

For Members of the General Public

Participation in the ADNeT Registry simply means:

  • allowing us to collect information about you and your health, and
  • being invited to complete surveys and/or participate in future research.

Participation is entirely voluntary.  To help you make an informed decision on participating in the Registry, please visit our FAQs page by clicking here.

FAQs for
Registry Clinicians and Staff at Participating Sites

For Clinicians and Participating Sites

Participation in the ADNeT Registry means collecting patient data (with their consent) and contributing to the Registry.

To learn more about the benefits of joining the ADNeT Registry, and find out about what you need to do to participate, please visit our FAQs page by clicking here.