Hoel Kari-Anne, Lichtwarck Bjørn, Væringstad Anette, Feiring Ingvild Hjorth, Rokstad Anne Marie Mork, Selbæk Geir, Benth Jūratė Šaltytė, Bergh Sverre
The Research Centre for Age-Related Functional Decline and Disease, Innlandet Hospital Trust, Ottestad, Norway.
Faculty of Medicine, University of Oslo, Oslo, Norway.
BMC Health Serv Res. 2022 Mar 29;22(1):415. doi: 10.1186/s12913-022-07830-9.
Behavioral and psychological symptoms of dementia (BPSD) occur frequently in people with dementia and can contribute to an increased need for help and a reduced quality of life, but also predict early institutionalization. The Targeted Interdisciplinary Model for Evaluation and Treatment of Neuropsychiatric Symptoms (TIME) might be a useful personalized approach to BPSD in people with dementia. The main objective of this feasibility trial was to explore the trial design and methods along with the patients' and the home care staff's acceptance of the TIME intervention before developing a definitive trial. Additionally, we wanted to explore whether TIME could be appropriate for staff in home care services in their approach towards people with dementia with anxiety and depression.
This was a 18-month feasibility trial using a parallel cluster randomized controlled design. Nine municipalities from the eastern part of Norway (clusters) - 40 people with dementia and 37 of their next of kin- were randomized to the TIME intervention or to treatment as usual. In addition, qualitative data as field notes were collected and summarized.
The staff in home care services experienced TIME as an appropriate method; in particular, the systematic approach to the patient's BPSD was experienced as useful. However, the completion of the assessment phase was considered exhaustive and time-consuming, and some of the staff found it challenging to find time for the case conferences.
We consider that TIME, with some adjustments, could be useful for staff in home care services in cases where they face challenges in providing care and support to people with dementia. This feasibility trial indicates that we can move forward with a future definitive randomized controlled trial (RCT) to test the effect of TIME in people with dementia receiving home care services.
ClinicalTrial.gov identifier: SI0303150608.
痴呆的行为和心理症状(BPSD)在痴呆患者中频繁出现,会导致对帮助的需求增加和生活质量下降,还预示着会较早地入住机构。神经精神症状评估与治疗的靶向跨学科模型(TIME)可能是一种针对痴呆患者BPSD的有用的个性化方法。在开展确定性试验之前,这项可行性试验的主要目的是探索试验设计和方法以及患者和家庭护理人员对TIME干预的接受程度。此外,我们想探讨TIME是否适合家庭护理服务人员用于应对患有焦虑和抑郁的痴呆患者。
这是一项为期18个月的可行性试验,采用平行整群随机对照设计。挪威东部的9个自治市(整群)——40名痴呆患者及其37名近亲——被随机分配接受TIME干预或常规治疗。此外,还收集并汇总了作为现场记录的定性数据。
家庭护理服务人员认为TIME是一种合适的方法;特别是,针对患者BPSD的系统方法很有用。然而,评估阶段的完成被认为详尽且耗时,一些工作人员发现很难抽出时间参加病例讨论会。
我们认为,经过一些调整后,TIME对于家庭护理服务人员在为痴呆患者提供护理和支持面临挑战的情况下可能是有用的。这项可行性试验表明,我们可以推进未来的确定性随机对照试验(RCT),以测试TIME对接受家庭护理服务的痴呆患者的效果。
ClinicalTrial.gov标识符:SI0303150608。