The involvement of patients and their families in healthcare policymaking has been a general trend in the recent years. This tendency can be observed also in the process of the current reform of psychiatric care in the Czech Republic, which should gradually shift the focus of psychiatric care from large facilities to community care.
Organisations representing patients and their families are among the stakeholders in this reform. The present poster analyses semi-structured in-depth interviews, documents, and observation notes with the objective to map and evaluate patient involvement in the reform from its launch to its implementation in 2012 - 2019.