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对一项针对居住在养老院的老年人的数字音乐和运动干预的随机对照试验的可行性进行的实际评估。

A realist evaluation of the feasibility of a randomised controlled trial of a digital music and movement intervention for older people living in care homes.

机构信息

Faculty of Health Sciences and Sport, University of Stirling, Stirling, FK4 9LA, Scotland, UK.

School of Cardiovascular and Metabolic Health, University of Glasgow, Glasgow, Scotland, UK.

出版信息

BMC Geriatr. 2023 Mar 6;23(1):125. doi: 10.1186/s12877-023-03794-5.

Abstract

BACKGROUND

Low physical activity in care home residents brings about negative mental health consequences, such as higher levels of depression and loneliness. With advancements in communication technology, particularly during the COVID-19 pandemic, the feasibility and effectiveness of a randomised controlled trial (RCT) of a digital Physical Activity (PA) resource in care homes deserve more research attention. A realist evaluation was used to uncover influencing factors of a feasibility study implementation to inform how a digital music and movement programme would work and under what circumstances this would be most effective.

METHODS

Participants were 49 older adults (aged 65 years +) recruited across ten care homes in Scotland. Surveys were administered at baseline and post-intervention comprising psychometric questionnaires on multidimensional health markers validated in older adults with possible cognitive impairment. The intervention comprised 12 weeks of four prescribed digitally delivered movement (n = 3) and music-only (n = 1) sessions per week. An activity coordinator delivered these online resources in the care home. Post-intervention focus groups with staff and interviews with a sub-sample of participants were conducted to gain qualitative data on the acceptability of the intervention.

RESULTS

Thirty three care home residents started the intervention, but only 18 residents (84% female) completed both pre- and post-intervention assessments. Activity coordinators (AC) offered 57% of the prescribed sessions, with an average residents' adherence of 60%. Delivery of the intervention did not go as planned due to Covid restrictions in care homes and delivery challenges, including (1) motivation and engagement, (2) changes in cognitive impairment and disabilities of the participants, (3) death or hospitalisation of the participants and (4) limited staffing and technology resources to deliver the programme as intended. Despite this, group participation and encouragement of residents supported the delivery and acceptance of the intervention, with ACs and residents reporting improved mood, physical health, job satisfaction and social support. Improvements with large effect sizes were found for anxiety, depression, loneliness, perceived stress and sleep satisfaction, but no changes in fear of falling, domains of general health or appetite.

CONCLUSION

This realist evaluation suggested that this digitally delivered movement and music intervention is feasible. From the findings, the initial programme theory was refined for future implementation of an RCT in other care homes but future research exploring how to tailor the intervention to those with cognitive impairment and/or lacking capacity to consent is needed.

TRIAL REGISTRATION

Retrospectively registered at ClinicalTrials.gov NCT05559203.

摘要

背景

养老院居民身体活动水平低会带来负面的心理健康后果,例如抑郁和孤独感水平升高。随着通信技术的进步,尤其是在 COVID-19 大流行期间,对养老院数字身体活动(PA)资源的随机对照试验(RCT)的可行性和有效性值得进行更多研究。本研究采用实际评估方法,以揭示实施可行性研究的影响因素,为数字音乐和运动计划的实施方式以及在何种情况下最有效提供信息。

方法

参与者为来自苏格兰 10 家养老院的 49 名年龄在 65 岁及以上的老年人。在基线和干预后进行了调查,调查内容包括针对可能有认知障碍的老年人进行多维健康标志物的心理测量问卷。干预措施包括每周进行 4 次数字交付的运动(n=3)和仅音乐(n=1),共 12 周。活动协调员在养老院提供这些在线资源。干预后,对工作人员进行焦点小组讨论,并对部分参与者进行访谈,以获取干预措施可接受性的定性数据。

结果

33 名养老院居民开始了干预,但只有 18 名居民(84%为女性)完成了干预前后的评估。活动协调员(AC)提供了 57%的预定课程,居民的平均参与率为 60%。由于养老院的新冠限制和交付挑战,干预措施的交付并不顺利,包括(1)动机和参与度,(2)参与者认知障碍和残疾的变化,(3)参与者死亡或住院,以及(4)有限的员工和技术资源来按计划交付该计划。尽管如此,小组参与和对居民的鼓励还是支持了干预措施的交付和接受,AC 和居民报告情绪、身体健康、工作满意度和社会支持得到改善。在焦虑、抑郁、孤独、压力感知和睡眠满意度方面发现了具有大效应量的改善,但在跌倒恐惧、一般健康领域和食欲方面没有变化。

结论

这项实际评估表明,这种数字交付的运动和音乐干预措施是可行的。根据研究结果,对初始方案理论进行了精炼,以便在其他养老院实施 RCT,但需要进一步研究如何针对认知障碍和/或缺乏同意能力的人调整干预措施。

试验注册

在 ClinicalTrials.gov 上进行了回顾性注册,编号为 NCT05559203。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/febe/9990241/9b19360e6253/12877_2023_3794_Fig1_HTML.jpg

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