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首页> 外文期刊>Trials >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
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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

机译:live@home.path-用痴呆症及其护理人员的家居居民人员的临床途径:用于混合方法,步进楔,随机对照试验的研究方案

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BACKGROUND: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.TRIAL REGISTRATION:ClinicalTrials.gov: NCT04043364. Registered on 15 March 2019.
机译:背景:痴呆症的全球健康挑战均为规模,成本和影响特殊。这是无法预防,治愈或大幅放缓,使疾病管理,护理人员支持和服务创新作为减少疾病负担的主要目标的唯一前十名死亡原因。尽管患者在家里兴奋地生活在家里,但患有患者的痴呆症人员的制度化是常见的。这种复杂的健康挑战是在日常临床实践中彻底实施的多组分干预措施。本文介绍了live@home.path试用的理由,开发,可行性测试和实现过程。方法:live@home.path试验是一个2年,多中心,混合方法,阶梯式楔形对照试验,旨在包括315个家居住宅人和他们的护理人员,从挪威的3个市内招募了痴呆症及其护理人员。阶梯式楔形随机化意味着所有Dyads都会收到干预,但是通过随机化确定时序。对照组构成等待干预的二元。与用户代表,研究人员和利益相关者合作制定了多组分干预,以满足2020年的国家痴呆计划计划的要求。在6个月的干预期间,参与者将分配给市政协调员,这是干预的核心特征,负责定期接触二元,以方便L:学习,我:创新,v:志愿者和e:赋予权力(Live)。主要结果是资源利用率。这是通过痴呆症(RUD)仪器和相对应力刻度(RSS)的资源利用来衡量的,反映了资源利用率超过关怀所需的实际时间,而且还有如何由Caregiver.discussion经历的任务经历的繁重:我们预计Live的实施导致痴呆治疗和护理的途径,与惯常的治疗相比,与治疗相比,并将支持高质量的独立生活,在家.Tirial注册:ClinicalTrials.gov:NCT04043364。 2019年3月15日注册。

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