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| Funder | European Commission |
|---|---|
| Recipient Organization | Stichting Het Nederlands Kanker Instituut-Antoni Van Leeuwenhoek Ziekenhuis |
| Country | Netherlands |
| Start Date | Oct 01, 2022 |
| End Date | Sep 30, 2027 |
| Duration | 1,825 days |
| Number of Grantees | 15 |
| Roles | Participant; Associated Partner; Coordinator |
| Data Source | European Commission |
| Grant ID | 101057482 |
STRONG-AYA is a new, interdisciplinary, multi-stakeholder European network to improve healthcare services, research and outcomes for Adolescents and Young Adults (AYA) with cancer, defined as individuals aged 15-39-years at cancer diagnosis.
AYAs with cancer form a unique group; they face age-specific issues (e.g. infertility, unemployment, financial problems) and decreased quality of life due to cancer and its treatment.
Unlike dedicated healthcare and trials for pediatric cancer patients, AYA-specific healthcare services are scarce and vary across Europe. AYAs who are at the core of society and economy need access to age-adjusted and high-quality healthcare.
AYA-care and research will benefit from collection and pooling of patient-centered data and collaboration among all stakeholders: patients, healthcare professionals, scientists, and policymakers.
Our consortium of clinical and scientific leaders in AYA-care, data science and registries, European Cancer Organisation, Youth Cancer Europe and EORTC will build on previous initiatives and EU grants.
Within STRONG-AYA we will set up a value-based healthcare research ecosystem to develop data-driven, interactive policy and visualization tools that bring, in co-creation with all stakeholders including patients, novel insights into AYA healthcare.
The project objectives, include: 1) Development of a Core Outcome Set (COS) for AYAs with cancer; 2) Implementation of the COS in 5 national healthcare systems (FR, IT, NL, UK, PL) and establish national infrastructures for outcome data management and clinical decision-making and a pan-European ecosystem that also welcomes future European countries; 3) Disseminate outcomes and facilitate interactions between national and pan-European stakeholders to develop data-driven analysis tools to process and present relevant outcomes, establish feedback loops for AYA cancer patients and the healthcare systems, and improve the reporting and assessment of outputs towards policy-makers.
Narodowy Instytut Onkologii Im. Marii Sklodowskiej-Curie -Panstwowy Instytut Badawczy; Stichting Integraal Kankercentrum Nederland; Institut Gustave Roussy; The University of Manchester; Ffund Bv; European Organisation for Research and Treatment of Cancer Aisbl; European Cancer Organisation; The Leeds Teaching Hospitals National Health Service Trust; Centre de Lutte Contre Le Cancer Leon Berard; Universiteit Maastricht; University of Leeds; Fundatia Youth Cancer Europe; Stichting Het Nederlands Kanker Instituut-Antoni Van Leeuwenhoek Ziekenhuis; University of Southampton; Fondazione Irccs Istituto Nazionale Dei Tumori
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