About this trial
WELL CARE aims to strengthen the supports available to informal carers and long-term care (LTC) workers for improving their resilience and mental wellbeing through care partnerships. The project consortium, lead by prof. Elizabeth Hanson (Linnaeus University) and consisting of six research organizations and nine national and European advocacy organizations, identifies good practices able to prevent or mitigate both occupational and non-occupational risks for informal carers' and LTC workers' resilience and mental wellbeing. On this basis, and under its Grant Agreement with the European Commission, the project team develops innovative solution prototypes, which will be transferable across different countries and contexts and guide stakeholders into the actual implementation in 5 European Union (EU) countries (Germany, Italy, Netherlands, Slovenia, Sweden), where the LTC sector presents dissimilar characteristics. Finally, the investigators will exploit the data and evidence collected and generated by WELL CARE to analyze related EU and national policies, and to formulate action-oriented recommendations for policy makers and stakeholders.
The current study protocol concerns the research activities within Work Package 3 of the project, particularly the activities during the Implementation and Evaluation Phase that runs from September 2026 until the end of 2027. During this phase the project team studies the results of local implementation partners' efforts who - building on the solution prototypes developed earlier in the WELL CARE project - develop and implement new supportive work and care practices. The investigators study the effects that implementing these practices brings about among participating caregivers in terms of mental wellbeing, resilience and care partnership dynamics, while also studying the implementation process itself to capture the processes, conditions and (organizational) contexts favorable to fostering care partnerships.
Eligibility criteria
Qualifiers
employed in a long-term care setting at one of the participating research sites;
directly involved in care provision or implementation of the new practices under study;
currently receiving care from long-term care workers and/or informal caregivers;
requiring support with everyday personal care and/or more complex daily tasks due to ageing, chronic illness, disability or frailty;
Disqualifiers
having a (permanent or temporary) psychiatric disorder or mental illness which makes the person unable to understand instructions and participate in the study activities;
experiencing circumstances that would make participation unduly burdensome (e.g., acute stress or illness);
providing care for fewer than the minimum number of hours required for inclusion; the threshold will be defined per country in a context-sensitive way, reflecting national differences and the characteristics of the implemented practices and their target populations;
only being involved in the provision or receiving of short-term or acute care (i.e., not long-term care);
Trial design
Treatments tested in this trial
- Solution Prototype in Germany
- Solution Prototype in Italy
- Solution Prototype in Slovenia
- Solution Prototype in Sweden
- Solution Prototype in the Netherlands
Treatment groups
Sponsors and collaborators
VU University of Amsterdam
Lead sponsor
Linnaeus University
Collaborator
University of Ljubljana
Collaborator
Istituto Nazionale di Ricovero e Cura per Anziani
Collaborator
Hochschule Zittau/Görlitz
Collaborator
European Commission
Collaborator