Advance Care Planning in Amyotrophic Lateral Sclerosis and other chronic life-limiting conditions: patients’ and family carers’ perspectives

Advance care planning in general practice and beyond – A cluster-randomized controlled trial of the ACP-GP intervention

Appropriateness of end-of-life care in children with serious illness: The development and measurement of pediatric-specific population-level quality indicators for big data

Doctoral project Elisabeth Honinx

Doctoral project Kim Beernaert

Doctoral project Sigrid Dierickx

Doctoral project Thijs Reyniers

eHealth support for people with serious illness and their family caregivers

Pediatric advance care planning for adolescents with cancer and their parents: the BOOST intervention and lessons learned

Support and wellbeing for people with serious illness and their family caregivers

Doctoral project Rebecca Verhofstede

Doctoral project Sarah Mroz

Pediatric advance care planning for adolescents with cancer and their parents: the BOOST intervention and lessons learned

Support and control in assisted dying and palliative sedation: current practices and potential for improvement

Using a health promotion approach and behavioral theories to gain insight into factors related to palliative care behaviors among people confronted with serious illness

CAPACITY: Flanders Project to Develop Capacity in Palliative Care Across Society

Developing and evaluating an eHealth application to develop palliative care capacity in people with advanced cancer and their family caregivers

DIAdIC - Evaluation of Dyadic Psychoeducational Interventions for People with Advanced Cancer and their Informal Caregivers: An international randomized controlled trial

End-of-life decisions in stillbirths, neonates and infants: a population-based study in Flanders, Belgium

Evaluating the impact of medical aid in dying on bereaved relatives: a prospective cohort study of grief, health consequences and bereavement care

Paediatric care at the end of life: a population-based analysis using quality indicators

Palliative care needs throughout the cancer journey

Palliative Care Research

Primary Care in a Compassionate Community (PRICCO). Towards a Paradigm Shift in Interdisciplinary and Multi-Sectional Primary Care to Improve the Quality of Life of Seriously ill and Frail Older People and their Families.

Towards theory-­based behavioral interventions to improve early initiation of palliative care in people with cancer: application of the Theory of Planned Behavior

What are the unmet care and support needs of children living with a parent diagnosed with advanced cancer: a mixed methods study using qualitative interviews, a quantitative survey and big data

Implementation of an evidence-informed practice guide for physicians to improve euthanasia practice in Dutch-speaking Belgium

The development, operationalisation and validation of a core outcome set for the evaluation of palliative sedation in clinical research and practice.

The relationship between palliative care and assisted dying: complexities and challenges in practice