Public Health Data

The first step towards a more citizen-centric data collection method is a better understanding of citizens’ motivations to provide or withdraw their permission. The purpose of this study is therefore to unravel if, why and under which circumstances citizens are willing to share their health-related data with governmental researchers. We aim to develop a data collection method that incorporates these citizen perspectives and build towards a high-quality public health database. This database will help policymakers better target, develop and evaluate public health interventions to eventually reduce the health inequalities in our society.

https://datainnovationhub.eu/projects/public-health-data/?tab=tab-overview