Linking Patients to Protocols: An Automated Registry Communication System Rachel Richesson, PhD, MPH University of South Florida College of Medicine 5th.

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Presentation transcript:

Linking Patients to Protocols: An Automated Registry Communication System Rachel Richesson, PhD, MPH University of South Florida College of Medicine 5th International Conference on Rare Diseases and Orphan Drugs Istituto Superiore di Sanità, Rome February 23-25, 2009

Rare Disease Clinical Research Network (RDCRN)

Consortium Website The consortium-specific public website provides the public with detailed information about the consortium and how to join the contact registry.

Consortium Registry Links The public consortium website contains a “join the registry” page that provides links to the registry for each disorder.

Registry Description

Learn More A “learn more” page has in depth material pertaining to the contact registry.

Authorization Agreement Registrants must agree to the HIPAA compliant authorization in order to register with the contact registry.

Registry Form The registration form contains information such as disorder, date of diagnosis, etc. The registrant enters their information into the web based form and registers with the Contact Registry.

Registry Acknowledgement Box

Registry Acknowledgement An acknowledge is sent to the registrant after they register or if they update their information. The registrant is provided with links in the to update their information.

Sample Study s can be sent to registrants by automations, schedules, or manually. The s can be customized to include content from each Consortium. A template is created to improve efficiency and quality.

Sample Study

Automated Communications Typical automations: –Welcome –New Study –New Clinical Site –Periodic (every 6 months) Automations can be customized by study or consortium

Administrator Interface: Campaign Manager

Administrator Interface: Campaign Configuration

Administrator Interface: Registrant Information and Updates

Enrollment ConsortiaN Angelman, Rett, & Prader-Willi Syndromes791 Bone Marrow Failure Disease387 Cholestatic Liver Disease290 Neurologic Channelopathies178 Genetic Diseases of Mucociliary Clearance276 Genetic Steroid Disorders60 Rare Lung Disease262 Rare Thrombotic Disease463 Urea Cycle Disorders281 Vasculitis1899 Total4887

Preferred Contact Method Contact MethodNPercent % Phone71515% Mail60712% Fax120% Missing531% %

Reported Referral Method How did you find out about us?NPercent Internet211945% Media70% Medical Professional4108% Missing291% Other1122% Publication1463% Support Group or Foundation186738% Word of mouth972% %

Aplastic Anemia & MDS International Foundation Mailing

Contact Registry’s Global Reach 10-15% of the Contact Registry have non- US, non-Canada Addresses Over 60 countries represented

Clinical Research Consortium Total # of Contact Registrants Eligible for Studies (% enrolled in selected studies) Within 200 miles of a clinical site Within 100 miles of a clinical site Total # of Contact Registrants Eligible for Studies (% enrolled in selected studies) Total # of Contact Registrants Eligible for Studies (% enrolled in selected studies) Angelman, Rett, & Prader-Willi 648 (15%)213 (20%)98 (29%) Bone Marrow Failures 282 (7%)96 (13%)46 (17%) Genetic Diseases of Mucociliary Clearance 315 (27%)52 (42%)32 (28%) Urea Cycle Disorders 207 (27%)97 (37%)68 (43%) Vasculitis 1325 (6%)482 (8%)229 (12%) All sampled studies (12, 2/23/2006) 2777 (12%)940 (16%)473 (21%) Enrollment on Clinical Studies

Summary Effective Patient-driven Automated Scalable

Future Directions Expand types of data collected –Define registry vs. (research) study? Additional diseases Additional sources for research studies Support community-based research

Acknowledgements NIH Office of Rare Diseases (ORD) NIH National Center for Research Resources (NCRR) RDCRN Coalition of Patient Advocacy Groups (CPAG) Ken Young Jennifer Lloyd Supported by Grant # RR from the NCRR, an NIH component, and the Office of Rare Diseases. Contents are solely the responsibility of the authors and do not necessarily represent the official views of NCRR or ORD or NIH.

Questions Jeffrey Krischer, PhD Rachel Richesson, PhD, MPH