Systematic review report and updates V2 (D2.3)
This report outlines progress in developing a state-of-the-art Knowledge Warehouse on the use of Patient Generated Health Data (PGHD) across multiple disease areas and stages of the patient journey. It presents updates to the initial umbrella review, enhancements to literature screening tools, including the use of Large Language Models, and systematic additions of recent reviews published between April 2024 and April 2025. The updated evidence base supports ongoing IMPROVE work packages, gap analysis, and next steps toward value-based, patient-centered healthcare.
Practices report and updates V2 (D2.7)
This second version of the Practices Report provides an updated overview of progress in identifying, analysing, and structuring real-world practices related to the collection and use of patient-generated health data within the IMPROVE project. It documents the expansion and methodological refinement of the practice tracker, strengthened links with European initiatives, and the inclusion of additional relevant IHI projects. The update enhances comparative analysis, stakeholder engagement, and explores AI-supported automation, supporting patient-centred, data-driven healthcare implementation across Europe.
Systematic review report and updates V1
In this report we elaborate on the protocol, which has been pre-registered at Prospero (https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=546427), for the extensive literature review we conducted together with the IMPROVE partners. This literature review is focused on the existing state-of-the-art scientific evidence about the use of Patient Generated Health Data PGHD in healthcare delivery, conceptual relations concerning PGHD in several disease areas throughout the patient's journey.
Practices report and updates V1
In this report we will provide the existing practices identification, monitoring and assessment. Within this task we will identify and analyse important practices across countries and regions, in order to develop a knowledge base of the existing practices that are conducted to develop methods or frameworks for collecting and using patient-generated health data. Data gathering will be done in existing repositories of good practices in different fields and with direct contacts with a wide range of leading regional and national ecosystems.
