SEACO Population Health Survey

SEACO Population Health and Census Surveys

The core projects are the data collections that SEACO designs, funds and conducts on a recurring basis. Together they enumerate a defined population, follow it over time, and record its health, social circumstances and deaths in a linked record now spanning more than a decade — the defining features of a Health and Demographic Surveillance System. Studies conducted on the platform build on this foundation, whether by analysing the data directly, sampling from the population register, or nesting new data collection within it. Four core projects make up this record, and access is available to researchers through SEACO's governed data access process.

A defining feature of these projects is linkage: consistent identifiers allow individuals and households to be followed across projects and over time. Researchers can analyse the existing data, nest new studies within the sampling frame, or link their own data collection to the longitudinal record. Selected indicators can also be explored through SEACO 360, the platform's interactive visualisation dashboard, prior to making a formal data request.

SEACO Individual Projects

Researchers use the SEACO infrastructure by securing national and international grants to finance and conduct individual projects within the SEACO cohort. Individual projects are specific research initiatives undertaken to address the priority questions identified by SEACO. These projects may analyse existing data, recruit participants from the population register for more detailed study, or collect new data nested within the surveillance framework and linked to the longitudinal record. All individual projects are conducted through SEACO's governed data access process and under the ethical and community engagement standards that apply across the platform.

To discuss access or bringing a project to the platform, contact the SEACO team at mum.seaco@monash.edu.