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针对匈牙利老年人群体 COVID-19 疫情健康损害的个性化健康教育(PROACTIVE-19):一项适应性随机对照临床试验方案。

Personalised health education against health damage of COVID-19 epidemic in the elderly Hungarian population (PROACTIVE-19): protocol of an adaptive randomised controlled clinical trial.

机构信息

Institute for Translational Medicine, Medical School, University of Pécs, Szigeti út 12, Pécs, H-7624, Hungary.

Translational Medicine Foundation, Szeged, Hungary.

出版信息

Trials. 2020 Sep 29;21(1):809. doi: 10.1186/s13063-020-04733-0.

Abstract

BACKGROUND

Early reports indicate that COVID-19 may require intensive care unit (ICU) admission in 5-26% and overall mortality can rise to 11% of the recognised cases, particularly affecting the elderly. There is a lack of evidence-based targeted pharmacological therapy for its prevention and treatment. We aim to compare the effects of a World Health Organization recommendation-based education and a personalised complex preventive lifestyle intervention package (based on the same WHO recommendation) on the outcomes of the COVID-19.

METHODS

PROACTIVE-19 is a pragmatic, randomised controlled clinical trial with adaptive "sample size re-estimation" design. Hungarian population over the age of 60 years without confirmed COVID-19 will be approached to participate in a telephone health assessment and lifestyle counselling voluntarily. Volunteers will be randomised into two groups: (A) general health education and (B) personalised health education. Participants will go through questioning and recommendation in 5 fields: (1) mental health, (2) smoking habits, (3) physical activity, (4) dietary habits, and (5) alcohol consumption. Both groups A and B will receive the same line of questioning to assess habits concerning these topics. Assessment will be done weekly during the first month, every second week in the second month, then monthly. The composite primary endpoint will include the rate of ICU admission, hospital admission (longer than 48 h), and mortality in COVID-19-positive cases. The estimated sample size is 3788 subjects per study arm. The planned duration of the follow-up is a minimum of 1 year.

DISCUSSION

These interventions may boost the body's cardiovascular and pulmonary reserve capacities, leading to improved resistance against the damage caused by COVID-19. Consequently, lifestyle changes can reduce the incidence of life-threatening conditions and attenuate the detrimental effects of the pandemic seriously affecting the older population.

TRIAL REGISTRATION

The study has been approved by the Scientific and Research Ethics Committee of the Hungarian Medical Research Council (IV/2428- 2 /2020/EKU) and has been registered at clinicaltrials.gov ( NCT04321928 ) on 25 March 2020.

摘要

背景

早期报告表明,COVID-19 可能需要在 5-26%的情况下入住重症监护病房(ICU),总体死亡率可能上升至已确诊病例的 11%,特别是影响老年人。目前缺乏针对 COVID-19 的预防和治疗的循证靶向药物治疗。我们旨在比较世界卫生组织(WHO)推荐的基于教育和个性化综合预防生活方式干预方案(基于相同的 WHO 建议)对 COVID-19 结局的影响。

方法

PROACTIVE-19 是一项实用、随机对照临床试验,采用自适应“样本量重新估计”设计。将对年龄在 60 岁以上且未确诊 COVID-19 的匈牙利人群进行调查,以自愿参加电话健康评估和生活方式咨询。志愿者将被随机分为两组:(A)一般健康教育组和(B)个性化健康教育组。参与者将经历 5 个领域的提问和建议:(1)心理健康,(2)吸烟习惯,(3)身体活动,(4)饮食习惯和(5)饮酒习惯。A 组和 B 组都将接受关于这些主题的习惯的相同问题询问。在第一个月每周评估一次,第二个月每两周评估一次,然后每月评估一次。主要复合终点包括 COVID-19 阳性病例的 ICU 入住率、住院时间(超过 48 小时)和死亡率。估计的样本量为每个研究臂 3788 例。预计随访时间至少为 1 年。

讨论

这些干预措施可以增强身体的心血管和肺储备能力,从而提高对 COVID-19 造成的损害的抵抗力。因此,生活方式的改变可以降低危及生命的疾病的发病率,并减轻严重影响老年人群的大流行的不利影响。

试验注册

该研究已获得匈牙利医学研究委员会科学和研究伦理委员会的批准(IV/2428-2 /2020/EKU),并于 2020 年 3 月 25 日在 clinicaltrials.gov 注册(NCT04321928)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/19bb/7523055/cf7be59f7905/13063_2020_4733_Fig1_HTML.jpg

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