CORDIS oferuje możliwość skorzystania z odnośników do publicznie dostępnych publikacji i rezultatów projektów realizowanych w ramach programów ramowych HORYZONT.
Odnośniki do rezultatów i publikacji związanych z poszczególnymi projektami 7PR, a także odnośniki do niektórych konkretnych kategorii wyników, takich jak zbiory danych i oprogramowanie, są dynamicznie pobierane z systemu OpenAIRE .
Rezultaty
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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)Guidelines and rules for the coordination, reporting and quality control of the project
Pilot study midterm recruitment report - Denmark-DTU-Children (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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 (odnośnik otworzy się w nowym oknie)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
Publikacje
Autorzy:
Poelarends, R.J.
Wydawca:
NA
Autorzy:
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
Opublikowane w:
BMJ Open, Numer 14, 2024, ISSN 2044-6055
Wydawca:
BMJ
DOI:
10.1136/bmjopen-2023-083558
Autorzy:
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
Opublikowane w:
BMJ Open, Numer 14, 2024, ISSN 2044-6055
Wydawca:
BMJ
DOI:
10.1136/bmjopen-2023-080644
Autorzy:
Jihan Halimiabc , Tiziana de-Magistris ab , Belinda López-Galánd
Wydawca:
NA
Autorzy:
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.
Wydawca:
PROSPERO
Autorzy:
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
Wydawca:
OSF
DOI:
10.17605/OSF.IO/M2KC4
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