• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

基于家庭的主动视频游戏方案对年轻囊性纤维化患者的疗效。

Effectiveness of a Home-Based Active Video Game Programme in Young Cystic Fibrosis Patients.

机构信息

Departamento de Fisioterapia, Motion in Brains Research Group, Centro Superior de Estudios Universitarios La Salle, Universidad Autónoma de Madrid, Madrid, Spain.

出版信息

Respiration. 2018;95(2):87-97. doi: 10.1159/000481264. Epub 2017 Oct 19.

DOI:10.1159/000481264
PMID:29045949
Abstract

BACKGROUND

Exercise-based rehabilitation is already a part of cystic fibrosis (CF) treatment; however, patient adherence is low.

OBJECTIVES

To assess the effectiveness of a home exercise programme using active video games (AVGs) as a training modality for children and adolescents with CF.

METHODS

Thirty-nine children with CF were randomised to a control group (CG, n = 20, age 11 ± 6 years; FEV1 86.2 ± 20.5% of predicted) or a training group (AVGG, n = 19, age 13 ± 3 years; FEV1 82.7 ± 21.7% of predicted). The home training protocol consisted of 30- to 60-min sessions, 5 days/week, for 6 weeks using a Nintendo Wii™ platform. Exercise capacity was measured by the 6-min walk test (6MWT) and modified shuttle walk test (MSWT); muscular strength was estimated using the horizontal jump test (HJT), medicine ball throw (MBT), and hand grip strength (right [RHG]; left [LHG]); and quality of life was rated using the Cystic Fibrosis Questionnaire-Revised (CFQ-R). All the children were measured at baseline, after rehabilitation, and at 12 months.

RESULTS

For the group × time interaction ANOVAs, the AVGG showed significant between-group differences in exercise capacity: 6MWT farthest walking distance, 38.4 m (p < 0.01); MSWT farthest walking distance, 78.4 m (p < 0.05); and muscular strength: HJT 9.8 cm, MBT 30.8 cm, RHG 7 kg, and LHG 6.5 kg (p < 0.01), before versus after intervention. The CFQ-R reported significantly higher scores on respiratory symptoms after the intervention and favoured the AVGG, and there was an improvement in other domains after 12 months. Adherence to the home exercise programme was 95% during the 6- week intervention period.

CONCLUSION

A home-based programme using AVGs can effectively improve exercise capacity, muscular strength and quality of life in the short-term in children and adolescents with CF. The effects of training on muscle performance and quality of life were sustained over 12 months.

摘要

背景

运动康复已经成为囊性纤维化(CF)治疗的一部分,但患者的依从性很低。

目的

评估使用主动视频游戏(AVG)作为培训模式对 CF 患儿和青少年进行家庭锻炼计划的效果。

方法

39 名 CF 患儿被随机分为对照组(CG,n = 20,年龄 11 ± 6 岁;FEV1 预测值的 86.2 ± 20.5%)或训练组(AVGG,n = 19,年龄 13 ± 3 岁;FEV1 预测值的 82.7 ± 21.7%)。家庭训练方案包括使用任天堂 Wii™平台进行 30 至 60 分钟/次,每周 5 天,共 6 周。运动能力通过 6 分钟步行测试(6MWT)和改良 shuttle 步行测试(MSWT)进行测量;肌肉力量使用水平跳跃测试(HJT)、药球投掷(MBT)和手握力(右手[RHG];左手[LHG])进行评估;生活质量使用囊性纤维化问卷修订版(CFQ-R)进行评估。所有患儿均在基线、康复后和 12 个月时进行测量。

结果

对于组×时间交互方差分析,AVGG 在运动能力方面显示出显著的组间差异:6MWT 最远步行距离,38.4m(p < 0.01);MSWT 最远步行距离,78.4m(p < 0.05);肌肉力量:HJT 9.8cm,MBT 30.8cm,RHG 7kg,LHG 6.5kg(p < 0.01),干预前与干预后。CFQ-R 在干预后报告呼吸症状的评分显著升高,并且有利于 AVGG,并且在 12 个月后其他领域也有所改善。家庭锻炼计划的依从性在 6 周干预期间为 95%。

结论

在家中使用 AVG 进行的计划可以在短期内有效提高 CF 患儿和青少年的运动能力、肌肉力量和生活质量。训练对肌肉性能和生活质量的影响在 12 个月后仍能持续。

相似文献

1
Effectiveness of a Home-Based Active Video Game Programme in Young Cystic Fibrosis Patients.基于家庭的主动视频游戏方案对年轻囊性纤维化患者的疗效。
Respiration. 2018;95(2):87-97. doi: 10.1159/000481264. Epub 2017 Oct 19.
2
Physiological response during activity programs using Wii-based video games in patients with cystic fibrosis (CF).使用基于 Wii 的视频游戏进行活动项目时囊性纤维化 (CF) 患者的生理反应。
J Cyst Fibros. 2014 Dec;13(6):706-11. doi: 10.1016/j.jcf.2014.05.004. Epub 2014 Jun 13.
3
Six minute walk test versus incremental shuttle walk test in cystic fibrosis.囊性纤维化患者的6分钟步行试验与递增往返步行试验对比
Pediatr Int. 2016 Sep;58(9):887-93. doi: 10.1111/ped.12919. Epub 2016 Apr 28.
4
The 1-Minute Sit-to-Stand Test in Adults With Cystic Fibrosis: Correlations With Cardiopulmonary Exercise Test, 6-Minute Walk Test, and Quadriceps Strength.成年囊性纤维化患者的1分钟坐立试验:与心肺运动试验、6分钟步行试验及股四头肌力量的相关性
Respir Care. 2016 Dec;61(12):1620-1628. doi: 10.4187/respcare.04821. Epub 2016 Nov 15.
5
A comparison of respiratory and peripheral muscle strength, functional exercise capacity, activities of daily living and physical fitness in patients with cystic fibrosis and healthy subjects.囊性纤维化患者与健康受试者的呼吸和外周肌肉力量、功能运动能力、日常生活活动及身体素质比较。
Res Dev Disabil. 2015 Oct-Nov;45-46:147-56. doi: 10.1016/j.ridd.2015.07.020. Epub 2015 Aug 1.
6
Active video gaming in primary ciliary dyskinesia: a randomized controlled trial.原发性纤毛运动障碍的主动视频游戏治疗:一项随机对照试验。
Eur J Pediatr. 2022 Aug;181(8):2891-2900. doi: 10.1007/s00431-022-04490-z. Epub 2022 May 10.
7
Effects of an educational intervention of physical activity for children and adolescents with cystic fibrosis: a randomized controlled trial.针对患有囊性纤维化的儿童和青少年进行体育活动教育干预的效果:一项随机对照试验。
Respir Care. 2015 Jan;60(1):81-7. doi: 10.4187/respcare.02578. Epub 2014 Aug 19.
8
Test-retest reliability, minimal detectable change and minimal clinically important differences in modified shuttle walk test in children and adolescents with cystic fibrosis.改良 shuttle 步行试验在儿童和青少年囊性纤维化中的重测信度、最小可检测变化和最小临床重要差异。
J Cyst Fibros. 2020 May;19(3):442-448. doi: 10.1016/j.jcf.2019.10.007. Epub 2019 Oct 31.
9
Minimal detectable change in six-minute walk test in children and adolescents with cystic fibrosis.六分钟步行试验在囊性纤维化患儿和青少年中的最小可检测变化。
Disabil Rehabil. 2021 Jun;43(11):1594-1599. doi: 10.1080/09638288.2019.1663947. Epub 2019 Sep 19.
10
Exercise programme in patients with cystic fibrosis: a randomized controlled trial.囊性纤维化患者的运动计划:一项随机对照试验。
Respir Med. 2014 Aug;108(8):1134-40. doi: 10.1016/j.rmed.2014.04.022. Epub 2014 Jun 26.

引用本文的文献

1
Effects of eHealth exercise on paediatric suppurative lung diseases: a systematic review and meta-analysis.电子健康运动对小儿化脓性肺部疾病的影响:一项系统评价和荟萃分析。
ERJ Open Res. 2025 Aug 26;11(4). doi: 10.1183/23120541.00977-2024. eCollection 2025 Jul.
2
Physical Training and Pulmonary Rehabilitation in Patients with Cystic Fibrosis: A Systematic Review and Meta-Analysis of Clinical Trials.囊性纤维化患者的体育锻炼与肺康复:一项临床试验的系统评价和荟萃分析
Healthcare (Basel). 2025 Aug 15;13(16):2017. doi: 10.3390/healthcare13162017.
3
Effects of a Tailored Home-Based Exercise Program, "KidMove", on Children with Cystic Fibrosis: A Quasi-Experimental Study.
一项针对囊性纤维化儿童的量身定制的居家锻炼计划“儿童运动”的效果:一项准实验研究。
Healthcare (Basel). 2024 Dec 24;13(1):4. doi: 10.3390/healthcare13010004.
4
Clinimetric properties of field exercise tests in cystic fibrosis: a systematic review.囊性纤维化现场运动测试的临床测量特性:一项系统综述。
Eur Respir Rev. 2024 Dec 18;33(174). doi: 10.1183/16000617.0142-2024. Print 2024 Oct.
5
Game-Based eHealth Interventions for the Reduction of Fatigue in People With Chronic Diseases: Systematic Review and Meta-Analysis.基于游戏的电子健康干预措施对慢性病患者疲劳的缓解作用:系统评价与荟萃分析
JMIR Serious Games. 2024 Oct 17;12:e55034. doi: 10.2196/55034.
6
Telerehabilitation in Children and Adolescents with Cystic Fibrosis: A Scoping Review.患有囊性纤维化的儿童和青少年的远程康复:一项范围综述。
Healthcare (Basel). 2024 May 8;12(10):971. doi: 10.3390/healthcare12100971.
7
Attitude Toward Virtual Rehabilitation and Active Video Games Among Therapists in Korea: A Nationwide Survey.韩国治疗师对虚拟康复和主动式电子游戏的态度:一项全国性调查。
Brain Neurorehabil. 2024 Jan 19;17(1):e4. doi: 10.12786/bn.2024.17.e4. eCollection 2024 Mar.
8
Telemedicine and Its Application in Cystic Fibrosis.远程医疗及其在囊性纤维化中的应用。
J Pers Med. 2023 Jun 25;13(7):1041. doi: 10.3390/jpm13071041.
9
Interventions for improving adherence to airway clearance treatment and exercise in people with cystic fibrosis.改善囊性纤维化患者气道清除治疗和运动依从性的干预措施。
Cochrane Database Syst Rev. 2023 Jul 18;7(7):CD013610. doi: 10.1002/14651858.CD013610.pub2.
10
Telehealth for children and adolescents with chronic pulmonary disease: systematic review.儿童和青少年慢性肺部疾病的远程医疗:系统评价。
Rev Paul Pediatr. 2023 May 15;42:e2024111. doi: 10.1590/1984-0462/2024/42/2022111. eCollection 2023.