Abstract

BackgroundTo understand user needs, system requirements and organizational conditions towards successful design and adoption of Clinical Decision Support Systems for Type 2 Diabetes (T2D) care built on top of computerized risk models.MethodsThe holistic and evidence-based CEHRES Roadmap, used to create eHealth solutions through participatory development approach, persuasive design techniques and business modelling, was adopted in the MOSAIC project to define the sequence of multidisciplinary methods organized in three phases, user needs, implementation and evaluation. The research was qualitative, the total number of participants was ninety, about five-seventeen involved in each round of experiment.ResultsPrediction models for the onset of T2D are built on clinical studies, while for T2D care are derived from healthcare registries. Accordingly, two set of DSSs were defined: the first, T2D Screening, introduces a novel routine; in the second case, T2D Care, DSSs can support managers at population level, and daily practitioners at individual level. In the user needs phase, T2D Screening and solution T2D Care at population level share similar priorities, as both deal with risk-stratification. End-users of T2D Screening and solution T2D Care at individual level prioritize easiness of use and satisfaction, while managers prefer the tools to be available every time and everywhere. In the implementation phase, three Use Cases were defined for T2D Screening, adapting the tool to different settings and granularity of information. Two Use Cases were defined around solutions T2D Care at population and T2D Care at individual, to be used in primary or secondary care. Suitable filtering options were equipped with “attractive” visual analytics to focus the attention of end-users on specific parameters and events. In the evaluation phase, good levels of user experience versus bad level of usability suggest that end-users of T2D Screening perceived the potential, but they are worried about complexity. Usability and user experience were above acceptable thresholds for T2D Care at population and T2D Care at individual.ConclusionsBy using a holistic approach, we have been able to understand user needs, behaviours and interactions and give new insights in the definition of effective Decision Support Systems to deal with the complexity of T2D care.

Highlights

  • To understand user needs, system requirements and organizational conditions towards successful design and adoption of Clinical Decision Support Systems for Type 2 Diabetes (T2D) care built on top of computerized risk models

  • By using a holistic approach, we have been able to understand user needs, behaviours and interactions and give new insights in the definition of effective Decision Support Systems to deal with the complexity of T2D care

  • A Decision Support Systems (DSS) for T2D Screening, hereinafter referred as Solution 1, for detection and prediction of the onset of the disease: a system to be built on top of intelligent risk-scores based on probabilistic models derived from dataset that, at present, are almost available from clinical studies;

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Summary

Introduction

System requirements and organizational conditions towards successful design and adoption of Clinical Decision Support Systems for Type 2 Diabetes (T2D) care built on top of computerized risk models. Most of the problems related to older age are linked to chronic diseases [1]. Healthcare systems are challenging the burden of chronic diseases by putting more emphasis on prevention, and by looking for new ways to reorient the provision of care in the light of the day-byday collected data. Individuals should be followed throughout the whole care process; their self-management role and capabilities must be clearly identified, together with the resources and services delivered by the healthcare system in relation to the stage of the disease. Diabetes represents one of the greatest health threats worldwide, with 425 million people affected. The disease can be asymptomatic, slowly evolving in a first phase but appearing with complications even before its diagnosis [3, 4]

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