The Center strives to advance the understanding, practice and development of palliative care in the Czech Republic through research, education and advocacy. Established in 2014, the Center has a team of academic, clinical and policy researchers who work together using various kinds of data and clinical experience to provide the best possible guidance for further development of palliative care.
The Center is the only non profit organisation in the Czech Republic focused specifically on academic and policy research in palliative care. The Center does not provide direct patient care but aims to facilitate a change in health and social care system through supporting care providers and policy makers in developing the most effective ways of helping patients at the end of life. We work in teams of researchers and healthcare professionals under the leadership of Dr Martin Loucka, who is also the founder of the organization. Oversight is provided by the board of trustees composed of 3 respected authorities from different areas of society, serving their role on honorary, unpaid basis.
The main areas of our research are the quality of life of patients with advanced disease and their families, and the evaluation of clinical and socioeconomic outcomes of palliative care. The results of our work are used to inform the development of clinical guidelines and to improve the evidence base of palliative care. Our team also works on policy research together with local councils, professional bodies and the government.
Center is involved in the development and delivery of various educational activities for professionals and the general public.
We strive to improve the public awareness and understanding of palliative care through various public campaigns, debates and collaboration with non-governmental and non-profit organizations. The Center also offers expert consultation services for policy makers and relevant institutions.
Martin Loucka, Center’s director, alumni of Lancaster University (UK) is currently a board member of the European Association for Palliative Care and works with several task forces and special interest groups across Europe.
We are part of an international consortium which received funding from the The EU Joint Programme – Neurodegenerative Disease Research (JPND) for a project called “Scaling up the Family Carer Decision Support Intervention: A multi-site implementation evaluation”.
We present the results of our work regularly at national and international conferences such as EAPC congresses. We are grateful that many international experts accepted our invitation in the past years (for example Sheila Payne, Sean Morrison, James Tulsky, Claudia Bausewein, Kevin Brazil, Fliss Murtagh) and came to share their expertise with the palliative care community in the Czech Republic.