
LSMU
9 Projects, page 1 of 2
Open Access Mandate for Publications and Research data assignment_turned_in Project2020 - 2025Partners:FUNDACIO CENTRE DE REGULACIO GENOMICA, ERASMUS MC, UM, UniPi, Siemens Healthcare GmbH +17 partnersFUNDACIO CENTRE DE REGULACIO GENOMICA,ERASMUS MC,UM,UniPi,Siemens Healthcare GmbH,SIEMENS HEALTHINEERS AG,EIBIR GEMEINNUETZIGE GMBH ZUR FOERDERUNG DER ERFORSCHUNG DER BIOMEDIZINISCHEN BILDGEBUNG,LSMU,LSMU,COLLECTIVE MINDS RADIOLOGY AB,EACR,ESOI,Umeå University,IDIBAPS-CERCA,Lynkeus (Italy),UB,UPV/EHU,MUG,ONCORADIOMICS,BSC,UNIV OF ARKANSAS,BBMRI-ERICFunder: European Commission Project Code: 952103Overall Budget: 9,994,360 EURFunder Contribution: 9,994,360 EURThe goal of EuCanImage is to build a highly secure, federated and large-scale European cancer imaging platform, with capabilities that will greatly enhance the potential of artificial intelligence (AI) in oncology. Firstly, the EuCanImage platform will be populated with a completely new data resource totaling over 25,000 single subjects, which will allow to investigate unmet clinical needs like never before, such as for the detection of small liver lesions and metastases of colorectal cancer, or for estimating molecular subtypes of breast tumours and pathological complete response. Secondly, the cancer imaging platform, built by leveraging the well-established Euro-Bioimaging infrastructure, will be cross-linked to biological and health repositories through the European Genome-phenome Archive, allowing to develop multi-scale AI solutions that integrate organ-level, molecular and other clinical predictors into dense patient-specific cancer fingerprints. To deliver this platform, the consortium will build upon several key European initiatives in data sharing for personalised medicine research, including EUCANCAn (cancer genomics and health data sharing), euCanSHare (cardiac imaging and omics data sharing) and EUCAN-Connect (federated data analytics). Furthermore, to foster international cooperation and leverage existing success stories, the consortium comprises the coordinators of The Cancer Imaging Archive (TCIA), the US cancer imaging repository funded by the National Cancer Institute. This will allow EuCanImage to leverage a unique 10-year long experience in cancer imaging storage, anonymisation, curation and management. Finally, a close collaboration between world renown clinical, radiomics, AI and legal experts within the consortium and beyond will establish well-needed guidelines for AI development and validation named FUTURE, for delivering Fair, Universal, Traceable, Usable, Robust and Explainable decision support systems for future cancer care.
more_vert Open Access Mandate for Publications and Research data assignment_turned_in Project2023 - 2026Partners:ULP , FIHCUV, IDIBAPS-CERCA, STRATEJAI, SERGAS +8 partnersULP ,FIHCUV,IDIBAPS-CERCA,STRATEJAI,SERGAS,UL,IPOPORTO,I3S - INSTITUTO DE INVESTIGACAO E INOVACAO EM SAUDE DA UNIVERSIDADE DO PORTO,LSMU,LSMU,CHU,ERASMUS MC,DiCEFunder: European Commission Project Code: 101095359Overall Budget: 6,334,800 EURFunder Contribution: 6,334,800 EURMost cases of gastric cancer (GC) are detected at a late stage, when patients have a median life expectancy of about a year. Diagnosing people at risk of developing GC at the pre-symptomatic stage, typically chronic gastric inflammation, could significantly improve the outlook. Artificial intelligence (AI) can help clinicians make sense of their own data by automating much of the treatment and analysis, which require manual work and years of experience. But it can do more: it can bring together available data from various sources into a vast data lake and cross-correlate the data to derive a ‘risk score’ for gastric cancer and shed light on the mechanisms of its evolution. Aida aims to do just that. It helps researchers understand the mechanisms that trigger gastric oncogenesis, helps clinicians diagnose precancerous inflammation at the earliest possible stage, suggests personalised therapeutic strategies for treatment and follow-up, and makes personalised recommendations for monitoring patient health status, thus contributing to gastric cancer prevention. This places Aida squarely on Europe’s agenda of ‘Staying healthy in a rapidly changing society’. Aida unites some of Europe’s leading authorities in the field of gastric inflammation, gastric cancer, leading AI and machine learning experts, experts on data governance and privacy, representatives of the public administration and patient advocates. Aida also has strong ties with the industry. After the project, the results will live on in an association that acts as a transnational focal point for chronic gastric inflammation — and GC in general. We hope that the solid, inclusive design principles of Aida, its societal relevance and its durability will spawn a vigorous ecosystem around chronic gastric inflammation, its understanding and its treatment. And we hope that it will inspire other data collaboratives in health — for other chronic inflammations, other forms of cancer or other ailments altogether.
more_vert Open Access Mandate for Publications and Research data assignment_turned_in Project2023 - 2028Partners:CESKA LEUKEMICKA SKUPINA - PROZIVOT, Z S, CING, MLU, IECSCYL, LSMU +15 partnersCESKA LEUKEMICKA SKUPINA - PROZIVOT, Z S,CING,MLU,IECSCYL,LSMU,OPBG,IRCCS,TIMELEX,IRST,GESELLSCHAFT FUR PADIATRISCHE ONKOLOGIE UND HAMATOLOGIE GGMH,UNIBO,TLS,LSMU,FONDAZIONE G.I.M.EM.A. - FRANCO MANDELLI ONLUS,ELN Foundation,OSHO, OSTDEUTSCHE STUDIENGRUPPE HAMATOLOGIE UND ONKOLOGIE E.V.,VHIR,HULAFE,Charité - University Medicine Berlin,MHHFunder: European Commission Project Code: 101104421Overall Budget: 5,988,400 EURFunder Contribution: 5,988,400 EURIn IMPACT-AML, a multidisciplinar R/R AML represents a model of high-impact disease, in which no standard of care exists, and where we have an urgent need for new evidence on possible therapies; AML offers the setting in which methodological innovation will combine powerful instruments of clinical trials with personalized medicine through academic efforts. Hereby, we propose to create an inclusive master framework for relapsed or refractory acute myeloid leukemia (STREAM) to include patients with R/R AML across Europe proficiently acquire an unselected population for clinical trials and monitor outcomes including neglected cohorts. Thereafter we will conduct a prospective randomized pragmatic clinical trial (RPCT) that will compare the classical “high intensity” rescue chemotherapy with biology-driven, “low intensity” rescue to obtain “real world” data on the benefit of one of the two different strategies in term of survival also considering patients and caregivers preferences, patient-reported outcomes (PRO), accessibility, affordability, and social cost. RPCT will aim to evaluate the effectiveness of real-world clinical alternatives in routine care. In addition to retaining the high internal validity of traditional randomized trials, it will maximize external validity, i. e. generalizability of results to many settings. In this context, the inclusion of an RPCT in the master framework will allow a dynamic inclusion and the collection of the excluded population as an instrument to predict the real-life applicability of clinical trial results. We will offer Europe results from an ambitious project, that will go beyond the state of the art in R/R AML demonstrating the superiority of a strategy in a first-of-his-kind clinical trial, providing strong data that will be delivered to national health care providers, policymakers, and health authorities data on optimized and affordable treatment for R/R AML and promoting the implementation of the selected better option. This action is part of the Cancer Mission cluster of projects on ‘Diagnosis and treatment’.
more_vert Open Access Mandate for Publications and Research data assignment_turned_in Project2022 - 2024Partners:EMPIRICA, i-HD, TICSALUT, LSMU, COCIR +10 partnersEMPIRICA,i-HD,TICSALUT,LSMU,COCIR,EUROPEAN PATIENTS FORUM,LSMU,OPTIMIT DOO,LUMC,ORCHA HEALTH BV,EUROHEALTHNET ASBL,ISS,EIT HEALTH EV,UvA,HIMSS EUROPE GMBHFunder: European Commission Project Code: 101057522Overall Budget: 1,999,960 EURFunder Contribution: 1,999,960 EURThere is a growing recognition that health and wellness apps need to play a much stronger role in health care systems, self-care and health prevention than they do today. However, health care systems, health professionals, patients and citizens lack means to adequately assess the quality and reliability of the many apps to choose from, for every purpose, in each app store. Suppliers experience the varying national approval processes as confusing and unclear as to what is expected and the depth of evidence that is required by each approval body. We intend to break through the impasse by leveraging the golden opportunity of the publication in July 2021 of the ISO 82304?2 Technical Specification (TS) and its health app quality label. Work is now needed to turn this globally endorsed quality assessment and health app quality label into the EU assessment and EU mHealth label, embed it within the approval and reimbursement processes of European countries and foster cross-country alignment of these approval processes. The objective of Label2Enable is threefold: achieve trust, use and adoption. We will pursue: 1. trust with an EU certification scheme that results in consistent compliant inclusive app assessments 2. use with: - a more detailed health app quality report that enables health professionals to recommend apps and insurers to speed up decisions on reimbursements - supporting communication that enables all patients, citizens and carers to use the label in considering health apps - social experimentation to promote app stores, app libraries and other routinely used trusted sources that (seek to) offer health apps to effectively publish the label alongside them 3. adoption of the TS and cross-country recognition with pilots, use stories, advocacy, mass communication and targeted multi-stakeholder engagement, affordable app assessments and a sustainable non-profit entity that will maintain the scheme, accredit app assessors and promote the TS after the project.
more_vert assignment_turned_in ProjectPartners:BCU, SIHTASUTUS TARTU UELIKOOLI KLIINIKUM, LSMU, The Czech Nurses Association, Osrodek Ksztalcenia Podyplomowego Pielegniarek i Poloznych +3 partnersBCU,SIHTASUTUS TARTU UELIKOOLI KLIINIKUM,LSMU,The Czech Nurses Association,Osrodek Ksztalcenia Podyplomowego Pielegniarek i Poloznych,PTK,LSMU,LINET spol. s r.o.Funder: European Commission Project Code: 2015-1-CZ01-KA202-014029Funder Contribution: 168,506 EURProject Goal: The project responded to the current situation in nursing staff training, specifically the situation in the field of Moving & Handling. Although there are many VET programs in this area, their impact on the incidence of musculoskeletal injuries / disorders in nursing staff is relatively low. There is a gap in the educational and training approaches, which would bring a shift in the training and change the moving and handling stereotypes brought by the old training methodologies. The aim of the project was therefore to transfer the innovative M&H training program developed by Birmingham City University from Great Britain to 4 European countries (to the Czech Republic, Poland, Estonia and Lithuania).Partnership: The main coordinator of the project was LINET, the leading European manufacturer of hospital and nursing beds, which is also very active in the VET of nurses worldwide. Other partners were Birmingham City University as a university that developed an innovative M&H programme, two nursing associations (Czech Association of Nurses, Polskie Towarzystwo Pielegniarskie), 1 nurse education centre (Osrodek Ksztalcenia Podyplomowego Pielegniarek i Poloznych) and 2 hospitals (Hospital of Lithuanian University of Health Sciences, Kaunas Clinics, SIHTASUTUS TARTU ULIKOOLI KLIINIKUM).Project activities: The project analysed the current state of education in the above mentioned areas and transferred an innovative VET program to 4 countries. Seminars for trainers were carried out and the innovative M&H educational program was then pilot tested. Afterwards, dissemination events took place mainly through the implementation of local workshops and small scale meetings. Within the project, several transnational project meetings were held. At the end of the project the impacts of the program on the target group were evaluated. In general, the target group stated that the use of these new manipulation techniques with patients greatly facilitates their current work, and the transfer and enforcement of these techniques in the educational processes are seen as entirely breakthrough. The nurses evaluated the training course as very beneficial and the target group agreed that the implementation of the project will increase the effectiveness of the education, the education process will be significantly upgraded and the implementation of these techniques among the medical personnel will reduce the number of injuries of the musculoskeletal system at the nursing staff. Outputs of the project: As a result of the implementation of the project a detailed analysis of the state of the art of the above-mentioned issues was carried out in individual countries. There was also carried out a research of the impact of the educational program, which served as input for the final creation of 4 local versions of the training course.The project ran in line with the scheduled timetable and was successfully completed in September 2017.
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