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Effectiveness of a digitally supported care management programme to reduce unmet needs of family caregivers of people with dementia: study protocol for a cluster randomised controlled trial (GAIN)

机译:数字支持的护理管理计划的有效性,减少痴呆症人民家庭照顾者的未满足需求:群体随机对照试验的研究议定书(GAIN)

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Up to two-thirds of dementia care is provided by family caregivers who often experience high burden, little support and adverse health outcomes. Enabling and supporting family caregivers to provide care at home prevents early institutionalisation of the person with dementia and alleviates the economic burden of dementia in the long term. General practitioners (GPs), as the first point of contact, have a key role in identifying and managing burden and care needs of family caregivers. However, in routine care, this opportunity is often limited by time constraints and even if caregiver needs are recognised, detailed information about regionally available support and advice on healthcare services is often lacking. This is a cluster randomised, controlled trial investigating the clinical use and cost-effectiveness of a digitally supported care management programme for caregivers of people with dementia (PwD). Five hundred family caregivers will be randomised at GP offices, specialist practices and memory clinics, with about n=250 participants per arm. Participants are eligible if they are the primary family caregiver of a PwD, are at least 18 years of age and provide informed consent. Participants in the intervention group will receive an individualised care management plan, which will be carried out by qualified study nurses in collaboration with the treating GP. All participants will receive a baseline assessment and a 6-months follow-up assessment. Participants in the wait-list control group will receive usual care. Starting at the 6 months’ follow-up, the former controls will also receive an individualised management plan. Primary outcomes are the number of unmet needs (incl. the Camberwell Assessment of Need for the Elderly, CANE) and health-related quality of life (EQ-5D-5L) at 6 months. Secondary outcomes include caregiver burden (Zarit Burden Interview, ZBI), social support (Lubben Social Network Scale, LSNS), the use of medical and non-medical services (Questionnaire for the Use of Medical and Non-Medical Services, FIMA) and resource utilisation (Resource Utilisation in Dementia, RUD). The primary analysis will be based on intention-to-treat. Between- and within-group analyses and a cost-effectiveness analysis will be conducted to estimate the effect of the tablet PC-based care management programme. This trial is funded by the German Federal Joint Committee (G-BA) Innovation Fund. The findings of this trial will be useful in informing and improving current healthcare system structures and processes to support family dementia caregivers within routine care practices. ClinicalTrials.gov NCT04037501 . Registered on 30 July 2019.
机译:家庭护理人员提供高达三分之二的痴呆症护理,他们经常经历高负担,小的支持和不良健康结果。支持和支持家庭照顾者在家提供护理可以防止人员早期制度化痴呆症,并在长期缓解痴呆症的经济负担。作为第一个联系人的全科医生(GPS)在识别和管理家庭照顾者的负担和照顾需求方面具有关键作用。然而,在常规护理中,这个机会通常受到时间限制的限制,即使认可护理人员需要,也往往缺乏关于区域可用支持和关于医疗服务的建议的详细信息。这是一组随机,受控试验调查患有痴呆症(PWD)的人的照顾者的临床使用和成本效益。五百家庭护理人员将在GP办公室,专业实践和记忆诊所随机分配,每只手臂大约n = 250名参与者。如果他们是PWD的主要家庭照顾者,参与者符合条件,年满18岁并提供知情同意。干预组的参与者将获得个性化护理计划,该计划将由合格的研究护士与治疗GP合作进行。所有参与者将获得基线评估和6个月的后续评估。等待列表控制组的参与者将获得通常的关怀。从6个月后续开始,前控制也将获得个性化管理计划。主要结果是未满足的需求(包括老年人,甘蔗)和与健康相关的生活质量(EQ-5D-5L)的数量有关的需求的数量。二次结果包括护理人员负担(Zarit负担访谈,ZBI),社会支持(Lubben社交网络规模,LSN),使用医疗和非医疗服务(用于使用医疗和非医疗服务,FIMA)和资源的问卷利用(痴呆症,RUD中的资源利用)。主要分析将基于意向治疗。将进行 - 内部分析与内部分析和成本效益分析,以估算基于平板电脑的护理管理计划的效果。该试验由德国联邦联合委员会(G-BA)创新基金资助。该试验的调查结果将有助于通知和改进当前的医疗保健系统结构和流程,以支持常规护理实践中的家庭痴呆护理人员。 ClinicalTrials.gov NCT04037501。 2019年7月30日注册。

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