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In order to promote sound management of research data the European Commission, under the Horizon 2020 framework program, is promoting the adoption of a Data Management Plan (DMP) in research projects. Despite the value of a DMP to make data findable, accessible, interoperable and reusable (FAIR) through time, the development and implementation of DMPs is not yet a common practice in health research. Raising the awareness of researchers in small projects to the benefits of early adoption of a DMP is, therefore, a motivator for others to follow suit. In this paper we describe an approach to engage researchers in the writing of a DMP, in an ongoing project, FrailSurvey, in which researchers are collecting data through a mobile application for self-assessment of fragility. The case study is supported by interviews, a metadata creation session, as well as the validation of recommendations by researchers. With the outline of our process we also outline tools and services that supported the development of the DMP in this small project, particularly since there were no institutional services available to researchers

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Background The small sample sizes available within many very preterm (VPT) longitudinal birth cohort studies mean that it is often necessary to combine and harmonise data from individual studies to increase statistical power, especially for studying rare outcomes. Curating and mapping data is a vital first step in the process of data harmonisation. To facilitate data mapping and harmonisation across VPT birth cohort studies, we developed a custom classification system as part of the Research on European Children and Adults born Preterm (RECAP Preterm) project in order to increase the scope and generalisability of research and the evaluation of outcomes across the lifespan for individuals born VPT. Methods The multidisciplinary consortium of expert clinicians and researchers who made up the RECAP Preterm project participated in a four-phase consultation process via email questionnaire to develop a topic-specific classification system. Descriptive analyses were calculated after each questionnaire round to provide pre- and post- ratings to assess levels of agreement with the classification system as it developed. Amendments and refinements were made to the classification system after each round. Results Expert input from 23 clinicians and researchers from the RECAP Preterm project aided development of the classification system's topic content, refining it from 10 modules, 48 themes and 197 domains to 14 modules, 93 themes and 345 domains. Supplementary classifications for target, source, mode and instrument were also developed to capture additional variable-level information. Over 22,000 individual data variables relating to VPT birth outcomes have been mapped to the classification system to date to facilitate data harmonisation. This will continue to increase as retrospective data items are mapped and harmonised variables are created. Conclusions This bespoke preterm birth classification system is a fundamental component of the RECAP Preterm project's web-based interactive platform. It is freely available for use worldwide by those interested in research into the long term impact of VPT birth. It can also be used to inform the development of future cohort studies.

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Experimental field campaigns for collecting wind data, essential for academic research and the wind energy industry, are non-trivial due to the complex equipment and infrastructure required. This paper reports the latest developments of the WindsPT e-Science platform for planning, executing, and disseminating wind measurement campaign data. Existing e-Science platforms have been developed for more generic domains, preventing them from capturing the details and requirements of the field. Additionally, we propose a protocol for transferring large volumes of data from the in-site devices to our platform, ensuring data replication. With an easy-to-use Web interface, WindsPT promotes collaboration between participants, disseminates results among the stakeholders, publishes metadata, uses DOI, and includes metadata that enables machine-to-machine communication. The platform has multiple sections, with maps, images, and documents, where there is information about the location of the stations, positioning of the sensors, operating dates, photos, technical sheets, calibration documents, among others. The WindsPT platform has been used to host the Perdigão 2017 experimental campaign and proved to be a valuable tool during all the phases of this large field experiment. A new version of WindsPT, designed to be FAIR, host multiple campaigns, and include multiple cross-campaign shared features, as full-text search capabilities, is now developed and tested.

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One of the most critical ICT application domains is healthcare, where a single failure can lead a patient into a hazardous situation. Due to this, there's a great necessity to ensure that the developed solutions are safe and secure and perform as expected. Smart-Health-4-All (SH4ALL) is a project aiming at accelerating the research, development, commercialization, and dissemination of trustworthy smart health solutions in Portugal. One of the key components of the project is a web platform that supports the generation of integration and system tests for smart health solutions (comprising medical devices, applications, etc.), following a software product line approach. At the domain engineering level, the platform supports the creation of feature models and related test patterns for families of smart health products. At the product engineering level, the platform supports the instantiation of test patterns and the generation of corresponding test scripts ready for execution on specific products under test. This paper presents the aforementioned test platform and test process, and the discovery of test patterns.