Our research focuses on understanding the determinants of health, potential etiological factors, health resource utilization, experiences and outcomes among individuals affected by complex chronic diseases.
Established in 2017, and in collaboration with the BC Women’s Complex Chronic Diseases Program patients are invited to participate in the CCDP Data Registry. A data registry is a repository (bank) of information that is intended to be accessed to use in future research over an extended period of time. The Data Registry team is currently enrolling patients who are new to the CCDP.
In order to generate a better understanding of these debilitating conditions the data registry aims to:
a) Better characterize the patient population of the CCDP and
b) Assess CCDP patients' outcomes over time
Participation is voluntary and greatly appreciated.
Principal Investigator: Dr. Luis Nacul
For more information about our research projects, publications and more, please visit our website:
Complex Chronic Diseases Research Program
