Die Suchmaschine für Unternehmensdaten in Europa

EU-Förderung (2.281.840 €): Festlegung internationaler Standards bei der Analyse der berichteten Patientenergebnisse und gesundheitsbezogenen Lebensqualitätsdaten in klinischen Krebsstudien Hor 04.12.2020 EU-Rahmenprogramm für Forschung und Innovation "Horizont"

Auf einen Blick

Text

Festlegung internationaler Standards bei der Analyse der berichteten Patientenergebnisse und gesundheitsbezogenen Lebensqualitätsdaten in klinischen Krebsstudien

Measuring and quantifying how a patient feels or functions during treatment is an important endpoint in cancer clinical trials. It is generally accepted that the collection of PRO data in cancer clinical trials allows the inclusion of the patient’s voice in the risk-benefit assessment of therapies. However, no standards exist on how to analyse, interpret or report health-related quality of life (HRQOL) and other patient-reported outcomes (PROs). This initiative wants to pursue efforts in addressing the urgent need for standardization, by setting clear and validated standards that are tailored to and endorsed by all relevant stakeholders. With a strong international and multi-stakeholder Consortium, the initiative aims at finding consensus on suitable methods to analyse valid PRO objectives in cancer randomized clinical trials (RCTs) and ways to communicate these PRO findings in a standardized way that is understandable to all. To achieve this aim, SISAQOL-IMI will identify valid PRO research objectives and match these with appropriate statistical methods for PRO analysis in cancer RCTs. Translation to the estimands framework will be provided. Furthermore, the possibility of extending these recommendations to single-arm trial designs will be explored. Recommendations on clinically meaningful change for PRO instruments, as well as design considerations and ways for assessing quality of collected PRO data will be developed, and tools and templates for presentation and visualization of PRO findings freely made available. Strong emphasis is put on continuous collaboration with patient advocacy representatives throughout the project. Increased interpretability, adoption and full use of PRO outcomes for all stakeholders is expected by providing consensus-based and validated recommendations and communication tools for PRO data, ultimately resulting in better communication and shared decision making, improved outcomes, treatment satisfaction and care.


Geförderte Unternehmen:

Firmenname Förderungssumme
Abbvie Inc. 0,00 €
Academisch Ziekenhuis Leiden 340.500 €
Adelphi Values Ltd. 0,00 €
Bayer AG 0,00 €
Boehringer Ingelheim Internationalgesellschaft mbH 0,00 €
Consorcio Mar Parc de Salut de Barcelona 0,00 €
Critical Path Institute Stichting 0,00 €
Direktoratet FOR Medisinske Produkter 0,00 €
ESD - Evaluation Software Development GmbH 8.000,00 €
European Society FOR Medical Oncology 0,00 €
Fundacion Publica Miguel Servet 22.940 €
Johns Hopkins University 0,00 €
Katholieke Universiteit Leuven 153.500 €
Klinicki Bolnicki Centar Rijeka 62.700 €
Medizinische Universitat Innsbruck 564.500 €
Merck KGaA 0,00 €
Modus Outcomes SAS 0,00 €
Myeloma Patients Europe Aisbl 0,00 €
National Cancer Center 0,00 €
Organisation Europeenne Pour la Recherche et le Traitement du Cancer Aisbl 247.120 €
Oslo Universitetssykehus HF 527.460 €
Pfizer Ltd. 0,00 €
Queen's University AT Kingston 0,00 €
Region Hovedstaden 0,00 €
Stichting Amsterdam UMC 0,00 €
Stiftung FUR Qualitat UND Wirtschaftlichkeit IM Gesundheitswesen 0,00 €
THE Critical Path Institute (C-Path) NON Profit Corporation 0,00 €
THE European Medicines Agency 60.756 €
The University of Birmingham 0,00 €
THE University OF Sydney 0,00 €
Universitaetsklinikum Freiburg 34.124 €
Universiteit Gent 156.500 €
University Health Network 0,00 €
University of Leeds 103.740 €

Quelle: https://cordis.europa.eu/project/id/945052

Diese Bekanntmachung wurde von Englisch nach Deutsch übersetzt. Die Bekanntmachung bezieht sich auf einen vergangenen Zeitpunkt, und spiegelt nicht notwendigerweise den heutigen Stand wider.