ArticleJMIR mHealth and uHealth2020
Human-Centered Design Strategies for Device Selection in mHealth Programs: Development of a Novel Framework and Case Study.
Article in JMIR mHealth and uHealth, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 2 of them syntheses that pooled it.
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Who cites it
20 citing papers in PubMed, 2 syntheses or guidelines pooled it.
- Implementation of Machine Learning Applications in Health Care Organizations: Systematic Review of Empirical Studies.Journal of medical Internet research · 2024Pooled it
- Digitalized transcranial electrical stimulation: A consensus statement.Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology · 2022Pooled it
- Patient-centered gastrointestinal function assessment technologies: a paradigm shift from traditional approaches to non-invasive innovations.Frontiers in physiology · 2026Review
- Real-time biopsychosocial antecedents and correlates of functional neurological symptoms in daily life: A pilot remote monitoring technology study.Psychiatry research · 2024Article
- "Notification! You May Have Cancer." Could Smartphones and Wearables Help Detect Cancer Early?JMIR cancer · 2024Article
- Pre- and post-COVID 19 outbreak relationship between physical activity and depressive symptoms in Spanish adults with major depressive disorder: a secondary analysis of the RADAR-MDD cohort study.Frontiers in psychology · 2024Article
- The Role of a Smart Health Ecosystem in Transforming the Management of Chronic Health Conditions.Journal of medical Internet research · 2023Article
- Charting a Course for Smartphones and Wearables to Transform Population Health Research.Journal of medical Internet research · 2023Article
- Charting a course for smartphones and wearables to transform population health research.Journal of medical Internet research · 2023Article
- Non-equivalent, but still valid: Establishing the construct validity of a consumer fitness tracker in persons with multiple sclerosis.PLOS digital health · 2023Article
- Biopsychosocial Response to the COVID-19 Lockdown in People with Major Depressive Disorder and Multiple Sclerosis.Journal of clinical medicine · 2022Article
- Characteristics of Smart Health Ecosystems That Support Self-care Among People With Heart Failure: Scoping Review.JMIR cardio · 2022Article
- Developing an Unstructured Supplementary Service Data-based mobile phone app to provide adolescents with sexual reproductive health information: a human-centered design approach.BMC medical research methodology · 2022Article
- Data Visualization for Chronic Neurological and Mental Health Condition Self-management: Systematic Review of User Perspectives.JMIR mental health · 2022Review
- Exploring the Effects of In-App Components on Engagement With a Symptom-Tracking Platform Among Participants With Major Depressive Disorder (RADAR-Engage): Protocol for a 2-Armed Randomized Controlled Trial.JMIR research protocols · 2021Article
- Article
- Usability of a Mobile App for Real-Time Assessment of Fatigue and Related Symptoms in Patients With Multiple Sclerosis: Observational Study.JMIR mHealth and uHealth · 2021Observational
- Selecting Remote Measurement Technologies to Optimize Assessment of Function in Early Alzheimer's Disease: A Case Study.Frontiers in psychiatry · 2020Review
- The Role of Heart Rate Variability in the Future of Remote Digital Biomarkers.Frontiers in neuroscience · 2020Review
- Article
Corrections and comments
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Authors and funding
21 authors.
Funding
Abstract
backgroundDespite the increasing use of remote measurement technologies (RMT) such as wearables or biosensors in health care programs, challenges associated with selecting and implementing these technologies persist. Many health care programs that use RMT rely on commercially available, "off-the-shelf" devices to collect patient data. However, validation of these devices is sparse, the technology landscape is constantly changing, relative benefits between device options are often unclear, and research on patient and health care provider preferences is often lacking.
objectiveTo address these common challenges, we propose a novel device selection framework extrapolated from human-centered design principles, which are commonly used in de novo digital health product design. We then present a case study in which we used the framework to identify, test, select, and implement off-the-shelf devices for the Remote Assessment of Disease and Relapse-Central Nervous System (RADAR-CNS) consortium, a research program using RMT to study central nervous system disease progression.
methodsThe RADAR-CNS device selection framework describes a human-centered approach to device selection for mobile health programs. The framework guides study designers through stakeholder engagement, technology landscaping, rapid proof of concept testing, and creative problem solving to develop device selection criteria and a robust implementation strategy. It also describes a method for considering compromises when tensions between stakeholder needs occur.
resultsThe framework successfully guided device selection for the RADAR-CNS study on relapse in multiple sclerosis. In the initial stage, we engaged a multidisciplinary team of patients, health care professionals, researchers, and technologists to identify our primary device-related goals. We desired regular home-based measurements of gait, balance, fatigue, heart rate, and sleep over the course of the study. However, devices and measurement methods had to be user friendly, secure, and able to produce high quality data. In the second stage, we iteratively refined our strategy and selected devices based on technological and regulatory constraints, user feedback, and research goals. At several points, we used this method to devise compromises that addressed conflicting stakeholder needs. We then implemented a feedback mechanism into the study to gather lessons about devices to improve future versions of the RADAR-CNS program.
conclusionsThe RADAR device selection framework provides a structured yet flexible approach to device selection for health care programs and can be used to systematically approach complex decisions that require teams to consider patient experiences alongside scientific priorities and logistical, technical, or regulatory constraints.
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