Support, Monitoring and Reminder Technology for Mild Dementia

External independent evaluator will deliver a report, evaluating the project's progress against provided indicators.

The 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 8

Half-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 9

Half-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 7

External independent evaluator will deliver a report, evaluating the project's progress against provided indicators.

Customisation guidance document

This 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 report

The 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 1

Half-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 report

This 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 2

The 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 8

External independent evaluator will deliver a report, evaluating the project's progress against provided indicators

Management Report 3

Halfyearly 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 6

Half-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 5

Half-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 report

This report will collate the feedback from 15 early adopter patients regarding the use of the application.

Pilot SOP

The 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 4

Half-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 7

Half-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 reports

A 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 Report

Living 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 9

External independent evaluator will deliver a report, evaluating the project's progress against provided indicators

Management Report 2

Half-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.

SMART4MD enabled tablets

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.

Case studies

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 website

The core project website. used for dissemination of project results and all other public deliverables.

Scientific publications

6 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.

Ethics approval

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.

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