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dc.contributor.authorTorrado Vidal, Juan Carlos
dc.contributor.authorHusebø, Bettina Elisabeth Franziska
dc.contributor.authorAllore, Heather G.
dc.contributor.authorErdal, Ane
dc.contributor.authorFæø, Stein Erik
dc.contributor.authorReithe, Haakon
dc.contributor.authorFørsund, Elise
dc.contributor.authorTzoulis, Charalampos
dc.contributor.authorPatrascu, Monica
dc.date.accessioned2023-01-31T12:55:13Z
dc.date.available2023-01-31T12:55:13Z
dc.date.created2022-10-27T12:12:04Z
dc.date.issued2022
dc.identifier.citationPLOS ONE. 2022, 17:e0275747 (10), 1-19.en_US
dc.identifier.issn1932-6203
dc.identifier.urihttps://hdl.handle.net/11250/3047434
dc.descriptionThis is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.en_US
dc.description.abstractBackground: Active ageing is described as the process of optimizing health, empowerment, and security to enhance the quality of life in the rapidly growing population of older adults. Meanwhile, multimorbidity and neurological disorders, such as Parkinson’s disease (PD), lead to global public health and resource limitations. We introduce a novel user-centered paradigm of ageing based on wearable-driven artificial intelligence (AI) that may harness the autonomy and independence that accompany functional limitation or disability, and possibly elevate life expectancy in older adults and people with PD. Methods: ActiveAgeing is a 4-year, multicentre, mixed method, cyclic study that combines digital phenotyping via commercial devices (Empatica E4, Fitbit Sense, and Oura Ring) with traditional evaluation (clinical assessment scales, in-depth interviews, and clinical consultations) and includes four types of participants: (1) people with PD and (2) their informal caregiver; (3) healthy older adults from the Helgetun living environment in Norway, and (4) people on the Helgetun waiting list. For the first study, each group will be represented by N = 15 participants to test the data acquisition and to determine the sample size for the second study. To suggest lifestyle changes, modules for human expert-based advice, machine-generated advice, and self-generated advice from accessible data visualization will be designed. Quantitative analysis of physiological data will rely on digital signal processing (DSP) and AI techniques. The clinical assessment scales are the Unified Parkinson’s Disease Rating Scale (UPDRS), Montreal Cognitive Assessment (MoCA), Geriatric Depression Scale (GDS), Geriatric Anxiety Inventory (GAI), Apathy Evaluation Scale (AES), and the REM Sleep Behaviour Disorder Screening Questionnaire (RBDSQ). A qualitative inquiry will be carried out with individual and focus group interviews and analysed using a hermeneutic approach including narrative and thematic analysis techniques. Discussion: We hypothesise that digital phenotyping is feasible to explore the ageing process from clinical and lifestyle perspectives including older adults and people with PD. Data is used for clinical decision-making by symptom tracking, predicting symptom evolution, and discovering new outcome measures for clinical trials.en_US
dc.language.isoengen_US
dc.publisherPublic Library of Science (PLOS)en_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectParkinson diseaseen_US
dc.subjectelderlyen_US
dc.subjectagingen_US
dc.subjectartificial Intelligenceen_US
dc.subjectsleepen_US
dc.subjectcaregiversen_US
dc.subjectgeriatric depressionen_US
dc.subjectheart rateen_US
dc.titleDigital phenotyping by wearable-driven artificial intelligence in older adults and people with Parkinson's disease: Protocol of the mixed method, cyclic ActiveAgeing studyen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright: © 2022 Torrado et alen_US
dc.source.pagenumber1-19en_US
dc.source.volume17en_US
dc.source.journalPLOS ONEen_US
dc.source.issue10en_US
dc.identifier.doi10.1371/journal.pone.0275747
dc.identifier.cristin2065586
dc.relation.projectNorges forskningsråd: 288164en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Navngivelse 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse 4.0 Internasjonal