CORDIS fournit des liens vers les livrables publics et les publications des projets HORIZON.
Les liens vers les livrables et les publications des projets du 7e PC, ainsi que les liens vers certains types de résultats spécifiques tels que les jeux de données et les logiciels, sont récupérés dynamiquement sur OpenAIRE .
Livrables
This report is due when 50% of the study population is recruited. The report shall include an overview of the number of participants recruited/pilot, issues in recruitment and, if applicable, detailed description of applied and planned measures to compensate if any incurred delay.
Pilot study initiation package - Spain-CITA-Young Adults (s’ouvre dans une nouvelle fenêtre)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study midterm recruitment report - Bulgaria-Virtech-Elderly (s’ouvre dans une nouvelle fenêtre)This report is due when 50% of the study population is recruited. The report shall include an overview of the number of participants recruited/pilot, issues in recruitment and, if applicable, detailed description of applied and planned measures to compensate if any incurred delay.
Pilot study midterm recruitment report - Italy-USG-Young Adults (s’ouvre dans une nouvelle fenêtre)This report is due when 50% of the study population is recruited. The report shall include an overview of the number of participants recruited/pilot, issues in recruitment and, if applicable, detailed description of applied and planned measures to compensate if any incurred delay.
Project Management Guidelines (s’ouvre dans une nouvelle fenêtre)Guidelines and rules for the coordination, reporting and quality control of the project
Pilot study midterm recruitment report - Denmark-DTU-Children (s’ouvre dans une nouvelle fenêtre)This report is due when 50% of the study population is recruited. The report shall include an overview of the number of participants recruited/pilot, issues in recruitment and, if applicable, detailed description of applied and planned measures to compensate if any incurred delay.
Pilot study midterm recruitment report - Spain-CITA-Elderly (s’ouvre dans une nouvelle fenêtre)This report is due when 50% of the study population is recruited. The report shall include an overview of the number of participants recruited/pilot, issues in recruitment and, if applicable, detailed description of applied and planned measures to compensate if any incurred delay.
Pilot study midterm recruitment report - Spain-CREDA-Children (s’ouvre dans une nouvelle fenêtre)This report is due when 50% of the study population is recruited. The report shall include an overview of the number of participants recruited/pilot, issues in recruitment and, if applicable, detailed description of applied and planned measures to compensate if any incurred delay.
Pilot study initiation package - Italy-USG-Young Adults (s’ouvre dans une nouvelle fenêtre)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study midterm recruitment report - Spain-IDISBA-Young Adults (s’ouvre dans une nouvelle fenêtre)This report is due when 50% of the study population is recruited. The report shall include an overview of the number of participants recruited/pilot, issues in recruitment and, if applicable, detailed description of applied and planned measures to compensate if any incurred delay.
Pilot study midterm recruitment report - Spain-IDISBA-Elderly (s’ouvre dans une nouvelle fenêtre)This report is due when 50% of the study population is recruited. The report shall include an overview of the number of participants recruited/pilot, issues in recruitment and, if applicable, detailed description of applied and planned measures to compensate if any incurred delay.
Pilot study midterm recruitment report - Portugal-UC-Young Adults (s’ouvre dans une nouvelle fenêtre)This report is due when 50% of the study population is recruited. The report shall include an overview of the number of participants recruited/pilot, issues in recruitment and, if applicable, detailed description of applied and planned measures to compensate if any incurred delay.
Pilot study midterm recruitment report - Portugal-UEV-Young Adults (s’ouvre dans une nouvelle fenêtre)This report is due when 50% of the study population is recruited. The report shall include an overview of the number of participants recruited/pilot, issues in recruitment and, if applicable, detailed description of applied and planned measures to compensate if any incurred delay.
Pilot study initiation package - Portugal-UEV-Young Adults (s’ouvre dans une nouvelle fenêtre)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study initiation package - Portugal-UC-Young Adults (s’ouvre dans une nouvelle fenêtre)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study initiation package - Bulgaria-RCNE-Elderly (s’ouvre dans une nouvelle fenêtre)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study initiation package - Portugal-UEV-Children (s’ouvre dans une nouvelle fenêtre)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study initiation package - Denmark-DTU-Children (s’ouvre dans une nouvelle fenêtre)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study initition package - Bulgaria-RCNE-Young Adults (s’ouvre dans une nouvelle fenêtre)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study initiation package - The Netherlands-TU/e-Children & Young Adults (s’ouvre dans une nouvelle fenêtre)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study initiation package - Spain-IDISBA-Children (s’ouvre dans une nouvelle fenêtre)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study midterm recruitment report - Germany-DFKI/BIPS-Children & Young Adults (s’ouvre dans une nouvelle fenêtre)This report is due when 50% of the study population is recruited. The report shall include an overview of the number of participants recruited/pilot, issues in recruitment and, if applicable, detailed description of applied and planned measures to compensate if any incurred delay.
Pilot study initiation package - Spain-CITA-Elderly (s’ouvre dans une nouvelle fenêtre)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study midterm recruitment report - Spain-IDISBA-Children (s’ouvre dans une nouvelle fenêtre)This report is due when 50% of the study population is recruited. The report shall include an overview of the number of participants recruited/pilot, issues in recruitment and, if applicable, detailed description of applied and planned measures to compensate if any incurred delay.
Pilot study initiation package - Bulgaria-RCNE-Children (s’ouvre dans une nouvelle fenêtre)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study initiation package - Germany-DFKI/BIPS-Children & Young adults (s’ouvre dans une nouvelle fenêtre)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study midterm recruitment report - Spain-CITA-Young Adults (s’ouvre dans une nouvelle fenêtre)This report is due when 50% of the study population is recruited. The report shall include an overview of the number of participants recruited/pilot, issues in recruitment and, if applicable, detailed description of applied and planned measures to compensate if any incurred delay.
Pilot study initiation package - Spain-CREDA-Children (s’ouvre dans une nouvelle fenêtre)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study inititation package - Italy-AOUBO-Liver and Kidney Transplant Recipients (s’ouvre dans une nouvelle fenêtre)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study midterm recruitment report - Portugal-UEV-Children (s’ouvre dans une nouvelle fenêtre)This report is due when 50% of the study population is recruited. The report shall include an overview of the number of participants recruited/pilot, issues in recruitment and, if applicable, detailed description of applied and planned measures to compensate if any incurred delay.
Pilot study initiation package - Spain-IDISBA-Elderly (s’ouvre dans une nouvelle fenêtre)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study initiation package - Bulgaria-Virtech-Children (s’ouvre dans une nouvelle fenêtre)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
CDTEC - plan (s’ouvre dans une nouvelle fenêtre)Comprehensive CDTEC plan with elements of the project identity, targeted events and actions including a mapping of actors to be targeted and a set of KPIs to monitor activities
Pilot study initiation package - Bulgaria-Virtech-Elderly (s’ouvre dans une nouvelle fenêtre)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Pilot study initiation package - Spain-IDISBA-Young Adults (s’ouvre dans une nouvelle fenêtre)A Submission package, prior to enrolment of first study participant, containing:- the final version of the study protocol as submitted to regulators / ethics committee(s);- a registration number of the clinical trial in a WHO or ICMJE-approved registry;- regulatory and ethics (if applicable institutional) approvals required for the enrolment of the first study participant from ethics committees and national competent authorities if applicable.
Detailed DMP describing various data types, datasets, data quality & privacy issues, data management procedures, IT infrastructure and the data governance model
Official release of fully functional OSP based on partner & user feedbacks
HealthyW8 public website (s’ouvre dans une nouvelle fenêtre)A public project website to disseminate non-confidential project content (reports, publications as part of our open access strategy, etc.) and training & education tools to the target audiences and to house a restricted access area for partners to share information
Publications
Auteurs:
Poelarends, R.J.
Éditeur:
NA
Auteurs:
Farhad Vahid, Coralie Dessenne, Josep A Tur, Cristina Bouzas, Yvan Devaux, Laurent Malisoux, Margalida Monserrat-Mesquida, Antoni Sureda, Mahesh S Desai, Jonathan D Turner, Elsa Lamy, Maria Perez-Jimenez, Gitte Ravn-Haren, Rikke Andersen, Sarah Forberger, Rajini Nagrani, Yacine Ouzzahra, Michele Filippo Fontefrancesco, Maria Giovanna Onorati, Gino Gabriel Bonetti, Tiziana de-Magistris, Torsten Bohn
Publié dans:
BMJ Open, Numéro 14, 2024, ISSN 2044-6055
Éditeur:
BMJ
DOI:
10.1136/bmjopen-2023-083558
Auteurs:
Sarah Forberger, Lucia A Reisch, Pieter van Gorp, Christoph Stahl, Lara Christianson, Jihan Halimi, Karina Karolina De Santis, Laurent Malisoux, Tiziana de-Magistris, Torsten Bohn
Publié dans:
BMJ Open, Numéro 14, 2024, ISSN 2044-6055
Éditeur:
BMJ
DOI:
10.1136/bmjopen-2023-080644
Auteurs:
Jihan Halimiabc , Tiziana de-Magistris ab , Belinda López-Galánd
Éditeur:
NA
Auteurs:
Dr Tiziana de Magistris. Ms Jihan Halimi. Belinda Lopez-Galán. Dr Krizia Ferrini. Professor Zein Kallas. Ms Suzan Evers. Dr Torsten Bohn. Dr Sarah Forberger.
Éditeur:
PROSPERO
Auteurs:
Sarah Forberger, Lucia A Reisch, P van Gorp, Ch Stahl, Lara Christianson, J Halimi, Karina Karolina De Santis, Laurent Malisoux, T De Magistris, Torsten Bohn
Éditeur:
OSF
DOI:
10.17605/OSF.IO/M2KC4
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