Empowering healthy lifestyle behaviour through personalised intervention portfolios to prevent and control obesity during vulnerable stages of life

Leistungen

Pilot study midterm recruitment report - Bulgaria-Virtech-Children

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

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

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

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

Guidelines and rules for the coordination, reporting and quality control of the project

Pilot study midterm recruitment report - Denmark-DTU-Children

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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-Virtech-Children

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

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

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.

Data Management Plan (DMP)

Detailed DMP describing various data types, datasets, data quality & privacy issues, data management procedures, IT infrastructure and the data governance model

Launch of the OSP

Official release of fully functional OSP based on partner & user feedbacks

HealthyW8 public website

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

Veröffentlichungen

Multicomponent (bio)markers for obesity risk prediction: a scoping review protocol

Autoren: 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
Veröffentlicht in: BMJ Open, Ausgabe 14, 2024, ISSN 2044-6055
Herausgeber: BMJ
DOI: 10.1136/bmjopen-2023-083558

‘Let me recommend… ’: use of digital nudges or recommender systems for overweight and obesity prevention—a scoping review protocol

Autoren: 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
Veröffentlicht in: BMJ Open, Ausgabe 14, 2024, ISSN 2044-6055
Herausgeber: BMJ
DOI: 10.1136/bmjopen-2023-080644

Leistungen

Veröffentlichungen

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