Abstract

BackgroundPrevious attempts to implement electronic Personal Health Records (ePHRs) underline the importance of stakeholder involvement. We describe the development of an ePHR for people with severe and enduring mental health problems, and provide a model of involving stakeholders throughout.MethodsThere were three stages to the development of the ePHR. These were 1) identifying and responding to user and clinical needs; 2) preliminary testing; and 3) preliminary implementation. Stakeholder involvement was pervasive in all stages. We collaborated with 133 stakeholders in the first stage, 13 in the second, and 26 in the third. On the micro-level, a service user researcher conducted much of the data collection and analysis. On the macro-level, a service user advisory group guided decisions throughout the project, and a service user was an active member of the project executive board and the implementation team.ResultsService users and clinicians preferred an interactive ePHR with features such as access to care plans and care notes, a mood tracker, patient reported outcomes feeding into the clinical record, and social networking features. Many of the above were constructed following consultation with the relevant professionals, however further consultation is required before building a social networking function or providing access to full care notes. Service users positively rated the usability of the ePHR. Drop-in sessions helped service users access technology and learn how to use the ePHR.ConclusionsWe outline four considerations for future developers of ePHRs: appeal, construction, ease of use, and implementation. Success rests on implementation in routine practice, so ePHRs must be intuitive and useful for both service users and staff. Continued involvement of end users throughout the design and testing process can help to achieve this goal.Electronic supplementary materialThe online version of this article (doi:10.1186/s12888-014-0305-9) contains supplementary material, which is available to authorized users.

Highlights

  • Previous attempts to implement electronic Personal Health Records underline the importance of stakeholder involvement

  • The current paper offers 1) a description of our electronic Personal Health Records (ePHRs); and 2) a model of service user inclusion in technology design and development

  • Setting and participants This ePHR was developed as part of the National Institute for Health Research (NIHR) Biomedical Research Centre, a partnership between South London and Maudsley National Health Service (NHS) Foundation Trust (SLaM) and the Institute of Psychiatry at King’s College London

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Summary

Introduction

Previous attempts to implement electronic Personal Health Records (ePHRs) underline the importance of stakeholder involvement. We describe the development of an ePHR for people with severe and enduring mental health problems, and provide a model of involving stakeholders throughout. Anyone who has used the National Health Service (NHS) within the UK has a clinical record detailing their medical history [1]. The advent of electronic Personal Health Records (ePHRs) changes this [2]. An ePHR may contain some of the information held within the clinical record, but it is accessed and maintained by the patient [2]. Patients typically access ePHRs online, through a patient portal.

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