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痴呆症歌唱试验性随机评估(PRESIDE):一项双臂、平行组随机对照可行性研究的方案,采用等待名单对照。

Pilot Randomised Evaluation of Singing in Dementia (PRESIDE): protocol for a two-arm, parallel-group randomised controlled feasibility study with waiting-list control.

作者信息

Dowson Becky, Schneider Justine, Guo Boliang, Bath Philip M, McDermott Orii, Haywood Lee J, Orrell Martin

机构信息

Institute of Mental Health, University of Nottingham, Jubilee Campus, Triumph Road, Nottingham, NG7 2TU, UK.

Stroke Trials Unit, Division of Clinical Neuroscience, University of Nottingham, Clinical Sciences Building, Nottingham, PB, NG5 1, UK.

出版信息

Pilot Feasibility Stud. 2021 Jan 7;7(1):15. doi: 10.1186/s40814-020-00759-y.

Abstract

BACKGROUND

As the number of people living with dementia grows, so does the need to provide them with adequate psychosocial support. Many people with dementia live at home with family carers, who also require social and emotional support to cope with their role. Community group singing has received attention for its potential to support people with dementia and their carers. It is postulated that singing can improve cognitive function, strengthen the bonds between care partners and help to establish social support networks. However, there is a lack of rigorous evidence of singing's benefits for this population. This study aims to test the feasibility of a randomised controlled trial of community singing in dementia, to pave the way for a larger, conclusive study.

METHODS

The PRESIDE study is designed as a two-arm, parallel-group randomised trial with a waiting list control. Dyads consisting of a person with dementia (n = 80) and their carer (n = 80) will be recruited. Each dyad will be randomised either to attend 10 weeks of community group singing sessions straight away or to wait for 3 months before attending the sessions. The singing sessions will be led by experienced professional musicians and will last about 90 min, including time for socialising. The primary outcome of this study is the attainment of feasibility criteria around recruitment, retention and the acceptability of the waiting list control. Secondary outcomes include the quality of life, mood, cognition, and musical engagement of the person with dementia, and quality of life, mood, and experiences/challenges of the carer. These data will be collected during home visits at baseline, and 3 and 6 months post-baseline.

DISCUSSION

Despite growing public interest in the positive effects of singing, and encouraging findings from qualitative and non-randomised quantitative studies, there is a lack of rigorous evidence. This is the first randomised controlled trial of community group singing for people with dementia in Europe, to our knowledge. If the results favour a full trial, conclusively demonstrating the effectiveness of group singing could positively affect the opportunities available to community-dwelling people with dementia and their carers.

TRIAL REGISTRATION

Unique identification number in ISRCTN registry: ISRCTN10201482 . Date registered: 12 May 2020.

摘要

背景

随着痴呆症患者数量的增加,为他们提供足够的心理社会支持的需求也在增长。许多痴呆症患者与家庭照顾者一起生活在家中,家庭照顾者也需要社会和情感支持来应对他们的角色。社区集体歌唱因其对痴呆症患者及其照顾者的支持潜力而受到关注。据推测,唱歌可以改善认知功能,加强照顾伙伴之间的联系,并有助于建立社会支持网络。然而,缺乏关于唱歌对这一人群益处的严格证据。本研究旨在测试针对痴呆症患者进行社区歌唱随机对照试验的可行性,为更大规模的确定性研究铺平道路。

方法

PRESIDE研究设计为双臂平行组随机试验,设有等待名单对照。将招募由痴呆症患者(n = 80)及其照顾者(n = 80)组成的二元组。每个二元组将被随机分配,要么立即参加为期10周的社区集体歌唱课程,要么等待3个月后再参加课程。歌唱课程将由经验丰富的专业音乐家带领,持续约90分钟,包括社交时间。本研究的主要结果是围绕招募、保留和等待名单对照的可接受性达到可行性标准。次要结果包括痴呆症患者的生活质量、情绪、认知和音乐参与度,以及照顾者的生活质量、情绪和经历/挑战。这些数据将在基线、基线后3个月和6个月的家访期间收集。

讨论

尽管公众对唱歌的积极影响兴趣日益浓厚,定性和非随机定量研究也有令人鼓舞的结果,但仍缺乏严格证据。据我们所知,这是欧洲首个针对痴呆症患者进行社区集体歌唱的随机对照试验。如果结果有利于全面试验,最终证明集体歌唱的有效性可能会对社区痴呆症患者及其照顾者可获得的机会产生积极影响。

试验注册

ISRCTN注册中心的唯一识别号:ISRCTN10201482。注册日期:2020年5月12日。

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