Risultati finali
External independent evaluator will deliver a report, evaluating the project's progress against provided indicators.
Preliminary report 1The report will release preliminary data about the use and benefits of SMARAT4MD, with trend analysis and tentative findings. The report will be disseminated widely to encourage external researchers to analyse the data in collaboration with the consortium partners.
Management Report 8Half-yearly report, summarising the project's progress, difficulties experienced, mitigation measures taken and lessons learned. This report will include an ethics report from the independent Ethics Advisor.
Management Report 9Half-yearly report, summarising the project's progress, difficulties experienced, mitigation measures taken and lessons learned. The report will include a short overview of expected tasks in the forthcoming half year.
Project Evaluation Report 7External independent evaluator will deliver a report, evaluating the project's progress against provided indicators.
Customisation guidance documentThis will be a practical document that explains how the SMART4MD platform can be adapted to the individual user's needs. This adaptation can be done by patients, carers or healthcare professionals, at any time during the lifetime of the platform. The document will include frequently asked questions, solutions for troubleshooting and contacts for further support by product specialists.
Final reportThe report will release final data about the use and benefits of SMART4MD, with full statistical analysis and policy recommendations. The report willl also highlight outstanding research questions from incidential findings during the project. The report will be disseminated widely to encourage external researchers to analyse the data in collaboration with the consortium partners.
Management Report 1Half-yearly report, summarising the project's progress, difficulties experienced, mitigation measures taken and lessons learned. The report will include a short overview of expected tasks in the forthcoming half year.
User acceptance reportThis report will collate the results of in-depth interviews with users, carers and healthcare professionals to explore their satisfaction with and perception of the SMART4MD platform and the study as a whole.
Preliminary report 2The report will release preliminary data about the use and benefits of SMART4MD, with trend analysis and tentative findings. The report will be disseminated widely to encourage external researchers to analyse the data in collaboration with the consortium partners.
Project Evaluation Report 8External independent evaluator will deliver a report, evaluating the project's progress against provided indicators
Management Report 3Halfyearly report summarising the projects progress difficulties experienced mitigation measures taken and lessons learned The report will include a short overview of expected tasks in the forthcoming half year This report will include an ethics report from the independent Ethics Advisor
Management Report 6Half-yearly report, summarising the project's progress, difficulties experienced, mitigation measures taken and lessons learned. The report will include a short overview of expected tasks in the forthcoming half year. This report will include an ethics report from the independent Ethics Advisor.
Management Report 5Half-yearly report, summarising the project's progress, difficulties experienced, mitigation measures taken and lessons learned. The report will include a short overview of expected tasks in the forthcoming half year.
Feasibility study reportThis report will collate the feedback from 15 early adopter patients regarding the use of the application.
Pilot SOPThe pilot Standard Operating Protocol will comprise: 1) Information sheet describing the nature of the pilot, in language and terms understandable to patients, carers and healthcare professionals. 2) Templates for informed consent, in language and terms understandable to patients, carers and healthcare professionals. 3) Inclusions and exclusion criteria for recruitment 4) Exit for participating patients. 5) Clinician handbook with: a) Best practice for patient recruitment b) Summary of data required for the pilot 6) Schedule for data collection. 7) Schedule for data analysis and feedback to healthcare professionals. The pilot SOP will be made public on our website and will be lodged with national clinical trial repositories to ensure full transparency of our pilot.
Management Report 4Half-yearly report, summarising the project's progress, difficulties experienced, mitigation measures taken and lessons learned. The report will include a short overview of expected tasks in the forthcoming half year.
Management Report 7Half-yearly report, summarising the project's progress, difficulties experienced, mitigation measures taken and lessons learned. The report will include a short overview of expected tasks in the forthcoming half year.
Focus group reportsA summary of all end-users (patient, carers and healthcare professionals), collating the focus groups' feedback on the phases of platform development and presenting a user-informed specification for the platform.
Accessibility ReportLiving documents compiling impact of users' medical condition on their ease of using SMART4MD, together with adaptation measures to improve accessibility for users.
Project Evaluation Report 9External independent evaluator will deliver a report, evaluating the project's progress against provided indicators
Management Report 2Half-yearly report, summarising the project's progress, difficulties experienced, mitigation measures taken and lessons learned. The report will include a short overview of expected tasks in the forthcoming half year.
600 tablets will be loaded with SMART4MD and locked to avoid improper use. The tablet will be delivered to the clinical partners, each partner receiving enough tablets to distribute to 50% of the local volunteers.
These will be easily accessible documents, presenting the pilot and results in each country to non-experts (e.g. policy makers, general public). Each case study will be written in the national language of the country of the pilot (English, Flemish, French, Spanish, Czech and Swedish) and will avoid using expert terminology or jargon. Each case study will refer to a scientific publication where additional details are presented; each case study will also offer local contact details for any enquiries.
SMART4MD project websiteThe core project website. used for dissemination of project results and all other public deliverables.
Scientific publications6 papers will be published to describe the results of the pilots on a national and European levels. Target journals include: Actas Españolas de Psiquiatria (Spanish pilot), British Medical Journal (UK pilot), Lékař a Technika (Czech pilot), Acta Clinica Belgica (Belgian pilot), Scandinavian Journal of Public Health (Swedish pilot) and Lancet (combined data from all pilots). For the benefit of project management, this deliverable will be considered complete when all manuscripts have been submitted to peer review in the relevant journals.
We will secure formal ethics approval in each country where we will run a pilot, viz. UK, Spain, Belgium, Sweden and Czech Republic. The deliverable will comprise: - Copies of the offical ethical approval letters from the Competent Authority in each country; - Copies of ethical approvals for the collection of personal data by the competent University Data Protection Officer or National Data Protection authority in each country.
Pubblicazioni
Autori:
Peter Anderberg, Pilar Barnestein-Fonseca, Jose Guzman-Parra, Maite Garolera, María Quintana, Fermin Mayoral-Cleries, Evi Lemmens, Johan Sanmartin Berglund
Pubblicato in:
JMIR Research Protocols, Numero 8/6, 2019, Pagina/e e13711, ISSN 1929-0748
Editore:
JMIR Res
DOI:
10.2196/13711
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