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dc.contributor.authorHusebø, Bettina
dc.contributor.authorAllore, Heather
dc.contributor.authorAchterberg, Wilco
dc.contributor.authorAngeles, Renira Corinne
dc.contributor.authorBallard, Clive
dc.contributor.authorBruvik, Frøydis Kristine
dc.contributor.authorFæø, Stein Erik
dc.contributor.authorGedde, Marie H.
dc.contributor.authorHillestad, Eirin
dc.contributor.authorJacobsen, Frode F.
dc.contributor.authorKirkevold, Øyvind
dc.contributor.authorKjerstad, Egil
dc.contributor.authorKjome, Reidun Lisbet Skeide
dc.contributor.authorMannseth, Janne
dc.contributor.authorNaik, Mala
dc.contributor.authorNouchi, Rui
dc.contributor.authorPuaschitz, Nathalie
dc.contributor.authorSamdal, Rune
dc.contributor.authorTranvåg, Oscar
dc.contributor.authorTzoulis, Charalampos
dc.contributor.authorVahia, Ipsit Vihang
dc.contributor.authorVislapuu, Maarja
dc.contributor.authorBerge, Line Iden
dc.date.accessioned2021-03-16T08:48:23Z
dc.date.available2021-03-16T08:48:23Z
dc.date.created2021-02-21T20:06:25Z
dc.date.issued2020
dc.identifier.citationHusebo, B. S., Allore, H., Achterberg, W., Angeles, R. C., Ballard, C., Bruvik, F. K., . . . Berge, L. I. (2020). LIVE@Home.Path—innovating the clinical pathway for home-dwelling people with dementia and their caregivers: study protocol for a mixed-method, stepped-wedge, randomized controlled trial. Trials, 21(1).en_US
dc.identifier.issn1745-6215
dc.identifier.urihttps://hdl.handle.net/11250/2733528
dc.description.abstractBackground The global health challenge of dementia is exceptional in size, cost and impact. It is the only top ten cause of death that cannot be prevented, cured or substantially slowed, leaving disease management, caregiver support and service innovation as the main targets for reduction of disease burden. Institutionalization of persons with dementia is common in western countries, despite patients preferring to live longer at home, supported by caregivers. Such complex health challenges warrant multicomponent interventions thoroughly implemented in daily clinical practice. This article describes the rationale, development, feasibility testing and implementation process of the LIVE@Home.Path trial. Methods The LIVE@Home.Path trial is a 2-year, multicenter, mixed-method, stepped-wedge randomized controlled trial, aiming to include 315 dyads of home-dwelling people with dementia and their caregivers, recruited from 3 municipalities in Norway. The stepped-wedge randomization implies that all dyads receive the intervention, but the timing is determined by randomization. The control group constitutes the dyads waiting for the intervention. The multicomponent intervention was developed in collaboration with user-representatives, researchers and stakeholders to meet the requirements from the national Dementia Plan 2020. During the 6-month intervention period, the participants will be allocated to a municipal coordinator, the core feature of the intervention, responsible for regular contact with the dyads to facilitate L: Learning, I: Innovation, V: Volunteering and E: Empowerment (LIVE). The primary outcome is resource utilization. This is measured by the Resource Utilization in Dementia (RUD) instrument and the Relative Stress Scale (RSS), reflecting that resource utilization is more than the actual time required for caring but also how burdensome the task is experienced by the caregiver. Discussion We expect the implementation of LIVE to lead to a pathway for dementia treatment and care which is cost-effective, compared to treatment as usual, and will support high-quality independent living, at home.en_US
dc.language.isoengen_US
dc.publisherBMCen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleLIVE@Home.Path--innovating the clinical pathway for home-dwelling people with dementia and their caregivers: Study protocol for a mixed-method, stepped-wedge, randomized controlled trialen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holder© The Author(s). 2020en_US
dc.source.volume21en_US
dc.source.journalTrialsen_US
dc.identifier.doi10.1186/s13063-020-04414-y
dc.identifier.cristin1892137
dc.source.articlenumber510en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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