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囊性纤维化患儿的力量训练与有氧运动训练:一项随机对照试验

Strength vs aerobic training in children with cystic fibrosis: a randomized controlled trial.

作者信息

Orenstein David M, Hovell Melbourne F, Mulvihill Mary, Keating Kristen K, Hofstetter C Richard, Kelsey Sheryl, Morris Kimberly, Nixon Patricia A

机构信息

Center for Behavioral Epidemiology and Community Health, 9245 Sky Park Court, Suite 230, San Diego, CA 92123, USA.

出版信息

Chest. 2004 Oct;126(4):1204-14. doi: 10.1378/chest.126.4.1204.

DOI:10.1378/chest.126.4.1204
PMID:15486384
Abstract

STUDY OBJECTIVE

Exercise has the potential to improve the ability of a patient with cystic fibrosis (CF) to cope with the physical demands of everyday life, and may improve prognosis. The purpose of this study was to compare the effects of a home-based, semi-supervised, upper-body strength-training regimen with a similarly structured aerobic training regimen.

DESIGN

Data were collected during a 1-year randomized clinical trial.

SETTING

Counselors conducted in-home visits with the participants once per week for the first 8 weeks followed by monthly visits for the remainder of the study.

PATIENTS

Sixty-seven patients with CF, aged 8 to 18 years, participated in the trial.

INTERVENTION

Participants in both exercise conditions were encouraged to exercise at least three times per week for 1 year. Each child in the aerobic group was given a stair-stepping machine, and each child in the upper-body strength training group was given an upper-body-only weight-resistance machine.

MEASURES AND RESULTS

Aerobic fitness, pulmonary function, quality of life, and strength were measured at baseline, at 6 months, and at 12 months. Strength training increased the maximum weight lifted for biceps curls significantly more than aerobic training (p < 0.02). However, this differential did not remain significant after control for increase in height. Both training procedures were associated with increased strength (p < 0.002) and physical work capacity (PWC) [p < 0.033].

CONCLUSIONS

We concluded that strength and aerobic training may increase upper-body strength, and that both types of training may increase PWC for children with CF. Future trials should be conducted with no-training control subjects and larger samples to increase statistical power.

摘要

研究目的

运动有可能提高囊性纤维化(CF)患者应对日常生活体力需求的能力,并可能改善预后。本研究的目的是比较家庭式、半监督的上肢力量训练方案与结构类似的有氧训练方案的效果。

设计

在一项为期1年的随机临床试验中收集数据。

设置

在研究的前8周,咨询师每周对参与者进行一次家访,之后在研究剩余时间每月进行一次家访。

患者

67名8至18岁的CF患者参与了试验。

干预

两种运动条件下的参与者都被鼓励每周至少锻炼3次,持续1年。有氧训练组的每个孩子都得到一台楼梯踏步机,上肢力量训练组的每个孩子都得到一台仅锻炼上肢的抗阻器械。

测量指标与结果

在基线、6个月和12个月时测量有氧适能、肺功能、生活质量和力量。力量训练使二头肌弯举的最大举重量增加,显著多于有氧训练(p < 0.02)。然而,在控制身高增加后,这种差异不再显著。两种训练方法都与力量增加(p < 0.002)和体力工作能力(PWC)增加(p < 0.033)相关。

结论

我们得出结论,力量训练和有氧训练可能会增加CF儿童的上肢力量,且两种训练都可能增加其PWC。未来的试验应以无训练对照组和更大样本进行,以提高统计效力。

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