Evaluation of an online intervention for improving stroke survivors’ health-related quality of life: A randomised controlled trial

IF 10.5 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL PLoS Medicine Pub Date : 2022-04-01 DOI:10.1371/journal.pmed.1003966
Ashleigh Guillaumier, N. Spratt, M. Pollack, A. Baker, P. Magin, A. Turner, C. Oldmeadow, Clare E Collins, R. Callister, Christopher Levi, A. Searles, S. Deeming, Brigid Clancy, B. Bonevski
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引用次数: 6

Abstract

Background The aim of this trial was to evaluate the effectiveness of an online health behaviour change intervention—Prevent 2nd Stroke (P2S)—at improving health-related quality of life (HRQoL) amongst stroke survivors at 6 months of follow-up. Methods and findings A prospective, blinded-endpoint randomised controlled trial, with stroke survivors as the unit of randomisation, was conducted between March 2018 and November 2019. Adult stroke survivors between 6 and 36 months post-stroke with capacity to use the intervention (determined by a score of ≥4 on the Modified Rankin Scale) and who had access and willingness to use the internet were recruited via mail-out invitations from 1 national and 1 regional stroke registry. Participants completed baseline (n = 399) and 6-month follow-up (n = 356; 89%) outcome assessments via computer-assisted telephone interviewing (CATI). At baseline the sample had an average age of 66 years (SD 12), and 65% were male. Randomisation occurred at the end of the baseline survey; CATI assessors and independent statisticians were blind to group allocation. The intervention group received remote access for a 12-week period to the online-only P2S program (n = 199; n = 28 lost at follow-up). The control group were emailed and posted a list of internet addresses of generic health websites (n = 200; n = 15 lost at follow-up). The primary outcome was HRQoL as measured by the EuroQol Visual Analogue Scale (EQ-VAS; self-rated global health); the outcome was assessed for differences between treatment groups at follow-up, adjusting for baseline measures. Secondary outcomes were HRQoL as measured by the EQ-5D (descriptive health state), diet quality, physical activity, alcohol consumption, smoking status, mood, physical functioning, and independent living. All outcomes included the variable ‘stroke event (stroke/transient ischaemic attack/other)’ as a covariate, and analysis was intention-to-treat. At 6 months, median EQ-VAS HRQoL score was significantly higher in the intervention group than the control group (85 vs 80, difference 5, 95% CI 0.79–9.21, p = 0.020). The results were robust to the assumption the data were missing at random; however, the results were not robust to the assumption that the difference in HRQoL between those with complete versus missing data was at least 3 points. Significantly higher proportions of people in the intervention group reported no problems with personal care (OR 2.17, 95% CI 1.05–4.48, p = 0.0359) and usual activities (OR 1.66, 95% CI 1.06–2.60, p = 0.0256) than in the control group. There were no significant differences between groups on all other secondary outcomes. The main limitation of the study is that the sample comprises mostly ‘well’ stroke survivors with limited to no disability. Conclusions The P2S online healthy lifestyle program improved stroke survivors’ self-reported global ratings of HRQoL (as measured by EQ-VAS) at 6-month follow-up. Online platforms represent a promising tool to engage and support some stroke survivors. Trial registration Australian New Zealand Clinical Trials Registry ACTRN12617001205325.
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在线干预对改善中风幸存者健康相关生活质量的评价:一项随机对照试验
本试验的目的是评估在线健康行为改变干预-预防第二次卒中(P2S) -在改善中风幸存者6个月随访时与健康相关的生活质量(HRQoL)方面的有效性。方法和发现2018年3月至2019年11月进行了一项前瞻性、盲终点随机对照试验,以中风幸存者为随机化单位。中风后6至36个月有能力使用干预措施的成年中风幸存者(由修正兰金量表得分≥4分确定),并有机会和意愿使用互联网,通过邮寄邀请从1个国家和1个地区中风登记处招募。参与者完成了基线(n = 399)和6个月的随访(n = 356;89%)通过计算机辅助电话访谈(CATI)进行结果评估。在基线时,样本的平均年龄为66岁(标准差12),65%为男性。随机化发生在基线调查结束时;CATI评估人员和独立统计人员对分组分配不知情。干预组接受为期12周的远程访问在线P2S计划(n = 199;随访时N = 28)。对照组通过电子邮件发送并张贴一份通用健康网站的地址列表(n = 200;随访时丢失15例)。主要终点是HRQoL,由EuroQol视觉模拟量表(EQ-VAS;自评全球健康);在随访中评估治疗组之间的差异,并根据基线测量进行调整。次要结局为HRQoL,以EQ-5D(描述性健康状态)、饮食质量、身体活动、饮酒、吸烟状况、情绪、身体功能和独立生活来衡量。所有结果包括变量“卒中事件(卒中/短暂性缺血性发作/其他)”作为协变量,分析是意向治疗。6个月时,干预组EQ-VAS HRQoL中位数评分显著高于对照组(85 vs 80,差异5,95% CI 0.79 ~ 9.21, p = 0.020)。对于数据随机丢失的假设,结果是稳健的;然而,结果并不足以证明数据完整者与缺失者的HRQoL差异至少为3分。干预组患者在个人护理(OR 2.17, 95% CI 1.05-4.48, p = 0.0359)和日常活动(OR 1.66, 95% CI 1.06-2.60, p = 0.0256)方面没有出现问题的比例明显高于对照组。各组间其他次要结果无显著差异。该研究的主要局限性在于,样本大多是“健康”的中风幸存者,只有有限的残疾或没有残疾。结论P2S在线健康生活方式项目改善了脑卒中幸存者在6个月随访时自我报告的HRQoL总体评分(以EQ-VAS测量)。在线平台是吸引和支持一些中风幸存者的一个很有前途的工具。澳大利亚新西兰临床试验注册中心ACTRN12617001205325。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
PLoS Medicine
PLoS Medicine 医学-医学:内科
CiteScore
21.60
自引率
0.60%
发文量
227
审稿时长
3 months
期刊介绍: PLOS Medicine aims to be a leading platform for research and analysis on the global health challenges faced by humanity. The journal covers a wide range of topics, including biomedicine, the environment, society, and politics, that affect the well-being of individuals worldwide. It particularly highlights studies that contribute to clinical practice, health policy, or our understanding of disease mechanisms, with the ultimate goal of improving health outcomes in diverse settings. Unwavering in its commitment to ethical standards, PLOS Medicine ensures integrity in medical publishing. This includes actively managing and transparently disclosing any conflicts of interest during the reporting, peer review, and publication processes. The journal promotes transparency by providing visibility into the review and publication procedures. It also encourages data sharing and the reuse of published work. Author rights are upheld, allowing them to retain copyright. Furthermore, PLOS Medicine strongly supports Open Access publishing, making research articles freely available to all without restrictions, facilitating widespread dissemination of knowledge. The journal does not endorse drug or medical device advertising and refrains from exclusive sales of reprints to avoid conflicts of interest.
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