Background: A paradigm shift in health care from illness to wellbeing requires new assessment technologies and intervention strategies. Self-monitoring tools based on the Experience Sampling Method (ESM) might provide a solution. They enable patients to monitor both vulnerability and resilience in daily life. Although ESM solutions are extensively used in research, a translation from science into daily clinical practice is needed. Objective: To investigate the redesign process of an existing platform for ESM data collection for detailed functional analysis and disease management used by psychological assistants to the general practitioner (PAGPs) in family medicine. Methods: The experience-sampling platform was reconceptualized according to the design thinking framework in three phases. PAGPs were closely involved in co-creation sessions. In the ‘understand’ phase, knowledge about end-users’ characteristics and current eHealth use was collected (nominal group technique – 2 sessions with N = 15). In the ‘explore’ phase, the key needs concerning the platform content and functionalities were evaluated and prioritized (empathy mapping – 1 session with N = 5, moderated user testing – 1 session with N = 4). In the ‘materialize’ phase, the adjusted version of the platform was tested in daily clinical practice (4 months with N = 4). The whole process was extensively logged, analyzed using content analysis, and discussed with an interprofessional project group. Results: In the ‘understand’ phase, PAGPs emphasized the variability in symptoms reported by patients. Therefore, moment-to-moment assessment of mood and behavior in a daily life context could be valuable. In the ‘explore’ phase, (motivational) functionalities, technological performance and instructions turned out to be important user requirements and could be improved. In the ‘materialize’ phase, PAGPs encountered barriers to implement the experience-sampling platform. They were insufficiently facilitated by the regional primary care group and general practitioners. Conclusion: The redesign process in co-creation yielded meaningful insights into the needs, desires and daily routines in family medicine. Severe barriers were encountered related to the use and uptake of the experience-sampling platform in settings where health care professionals lack the time, knowledge and skills. Future research should focus on the applicability of this platform in family medicine and incorporate patient experiences.
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Background: This paper describes the Co-Care-KIT, a reflective toolkit designed to provide insights into the diverse experiences of home-based informal caregivers during the delivery of care to a relative or loved one.Objective: The aim of this study was to evaluate the toolkit, including a custom-designed journal, tools for photography-based experience sampling, and heart rate tracking, which enables caregivers to collect and reflect on their positive and negative daily experiences in situ.Methods: A 2-week field study with informal caregivers (N=7) was conducted to evaluate the Co-Care-KIT and to capture their daily personal emotional experiences. The collected data samples were analyzed and used for collaborative dialogue between theresearcher and caregiver.Results: The results suggest that the toolkit (1) increased caregivers’ awareness of their own well-being through in situ reflection on their experiences; (2) empowered caregivers to share their identities and experiences as a caregiver within their social networks; (3) enabled the capturing of particularly positive experiences; and (4) provided caregivers reassurance with regards to their ownmental health.Conclusion: By enabling capturing and collaborative reflection, the kit helped to gain a new understanding of caregivers’ day-to-day needs and emotional experiences.
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In dit project werkt het lectoraat ‘Bewegen, gezondheid en welzijn’ samen met de Hogeschool Arnhem Nijmegen, Hogeschool Zuyd, de Vrije Universiteit, de Universiteit van Maastricht, het UMC Groningen, drie GGZ instellingen (Universitair Centrum Psychiatrie Groningen (UCP), GGZ Friesland en GGZ Drenthe), de Nederlandse Vereniging voor Psychomotorische Therapie en het Landelijk Platform Geestelijke Gezondheidzorg (LPGGZ, nu ook MIND). De projectdoelstelling is: Het verwerven van nieuwe kennis over de ontwikkeling en implementatie van specifieke uitkomstmaten waarmee de impact van psychomotorische interventies binnen de GGZ gemonitord en geëvalueerd kan worden en de samenwerking met de betrokken patiënt wordt versterkt. Aanleiding voor dit project zijn praktijkvragen van psychomotorisch therapeuten werkzaam in de GGZ. Zij geven aan behoefte te hebben aan nieuwe kennis en meetinstrumenten waarmee ze: 1. het behandelresultaat en de toenemende vraag naar evidentie van psychomotorische therapie (PMT) )vast kunnen stellen; 2. het beloop van de behandeling kunnen monitoren en bespreekbaar kunnen maken met de betrokken patiënt. Op basis van de beschikbare literatuur over behandelevaluaties werd de volgende onderzoeksvraag geformuleerd: ‘Hoe kunnen Patient Reported Outcome Measures (PROMs) voor psychomotorische therapie ontwikkeld en ingezet worden om het specifieke resultaat van psychomotorische therapie bij volwassen patiënten in de GGZ gestandaardiseerd te evalueren en wat kan de bijdrage zijn van dagboekmetingen via Experience Sampling Methods (ESM)?’. Het project richt zich op: 1. Selectie, onderzoek en onderbouwing van PMT specifieke PROMS. 2. Onderzoeken van de haalbaarheid van de inzet van ESM als evaluatiemethode binnen de PMT. 3. De ontwikkeling van een digitale portal. Beoogde resultaten zijn: • Databank van Nederlandstalige meetinstrumenten die als PROMs kunnen dienen ter evaluatie van pychomotorische interventies en die zijn opgenomen in een portal dat beschikbaar komt voor de beroepsgroep. • Handboek over het inzetten van ESM binnen PMT. • Cursussen over het gebruik van de PROMs en het gebruik van ESM.