在血压管理中使用exergames的对照试验中辍学率:一项系统回顾和荟萃分析方案

C. L. Lourenço, A. Barbosa, Vandrize Meneghini, A. Gerage
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引用次数: 0

摘要

Exergame是一种将体力消耗和游戏相结合的令人愉快的主动视频游戏,是一项技术创新,为健康领域带来了重要信息。在心血管领域,exergames已被用于控制成人血压,并取得了一些积极的结果。尽管如此,在初步研究中,有可能确定参与者退出了游戏干预,但迄今为止尚未产生综合证据来探索这一点。本综述的目的是:1)评估基于exerga的干预措施对成人和老年人静息血压的影响的对照试验的总退出率;Ii)比较实验组和对照组之间的辍学率,iii)调查与辍学率相关的干预特征。纳入标准:随机对照试验(rct)或准rct(≥4周)评估基于exerga的干预措施对≥18岁成人静息血压的影响。不受语言、出版日期和干预设置的限制。文献检索将使用PubMed、Scopus、SPORTDiscus、护理及相关健康文献累积索引、Web of Science、Cochrane Central Register of Controlled Trials和Science Electronic Library Online进行。随机对照试验的质量将使用Cochrane的偏倚风险工具进行评估。将提供汇总事件发生率(患病率)的描述性叙事综合和随机效应模型元分析(p < 0.05)。该协议的注册号为PROSPERO: CRD42020199547。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dropout rates in controlled trials with exergames for blood pressure management: a systematic review and meta-analysis protocol
Exergame, a type of enjoyable active video game that combines physical exertion and game is a technological innovation that has generated important information for the health field. In the cardiovascular area, exergames have been used to manage blood pressure in adults with some positive results. Despite this, in primary studies, it is possible to identify that participants dropout of the exergames interventions, but no synthesis of evidence has been produced so far to explore that. The aims of this review are i) to estimate the pooled rate of dropouts in controlled trials assessing the effects of exergame-based interventions on resting blood pressure in adults and older people; ii) to compare dropout rates between exergame and controls groups, and iii) to investigate the intervention characteristics associate with dropout rates. Inclusion criteria: Randomized controlled trials (RCTs) or quasi-RCTs (≥ 4 weeks) assessing the effects of exergame-based interventions on resting blood pressure in adults aged ≥ 18 years old. Without restriction to language, date of the publication, and intervention setting. Literature searches will be conducted using PubMed, Scopus, SPORTDiscus, Cumulative Index of Nursing and Allied Health Literature, Web of Science, Cochrane Central Register of Controlled Trials, and Scientific Electronic Library Online. The quality of the RCTs will be assessed using Cochrane’s risk of bias tool. A descriptive narrative synthesis and a random-effects model meta-analysis of the pooled event rate (prevalence) will be provided (p < 0.05). This protocol is registered with PROSPERO: CRD42020199547.
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