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运动干预可改善乳腺癌幸存者的身体疲劳感:一项随机临床试验。

Perceived physical fatigability improves after an exercise intervention among breast cancer survivors: a randomized clinical trial.

机构信息

Department of Epidemiology, University of Pittsburgh, Pittsburgh, PA, USA.

Department of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.

出版信息

Breast Cancer. 2022 Jan;29(1):30-37. doi: 10.1007/s12282-021-01278-1. Epub 2021 Jul 30.

Abstract

BACKGROUND

Among breast cancer populations, exercise interventions resulted in positive but relatively small improvements on fatigue, which may be due to insensitive measures of global fatigue. Perceived fatigability-whole-body tiredness anchored to standardized tasks/activities of a specific intensity and duration-may help to detect effective exercise interventions reducing fatigue in oncology. We examined whether perceived physical fatigability improved after an exercise intervention.

METHODS

This single center randomized clinical trial of 49 breast cancer survivors was conducted from 2015 to 2017, among which 41 participants (22 = exercise, 19 = control) completed the trial and reported their perceived physical fatigability at the first (Visit 1) and the last visit (Visit 3) over 6-14 weeks. Perceived physical fatigability was measured using the 10-item, self-administered Pittsburgh Fatigability Scale (PFS) scored 0-50. The mean differences of perceived physical fatigability between Visit 3 and Visit 1 were computed and compared by intervention groups using two sample t test.

RESULTS

Among the 41 women in the study (mean age 54.9 ± 9.8 years; 80% white), sociodemographic, clinical characteristics and baseline fatigue level were similar by intervention groups, except for antiestrogen use. Post-intervention changes (mean ∆ ± SE) of PFS Physical scores were greater in the exercise group (- 4.4 ± 1.4; - 22.5%) than the control group (0.2 ± 1.4; + 1.0%) (p = .022).

CONCLUSION

The PFS captured a reduction in fatigue after the exercise intervention among breast cancer survivors. These findings aid mounting efforts to reduce fatigue in oncology by introducing a more sensitive instrument to measure perceived physical fatigability to better evaluate patient-reported outcomes in future cancer trials.

TRIAL REGISTRATION

Clinicaltrials.gov identifier: NCT02770781.

摘要

背景

在乳腺癌患者群体中,运动干预措施可导致疲劳的改善,但改善效果较小,这可能是因为疲劳的整体测量指标不够敏感。感知疲劳能力——针对特定强度和持续时间的标准化任务/活动的全身性疲劳感——可能有助于检测出有效的运动干预措施,从而减轻肿瘤患者的疲劳感。我们研究了运动干预后感知身体疲劳能力是否会得到改善。

方法

这是一项在 2015 年至 2017 年间开展的单中心随机临床试验,共纳入 49 例乳腺癌幸存者,其中 41 例(22 例接受运动干预,19 例接受对照)完成了试验,并在 6-14 周内分别于首次(第 1 次就诊,Visit 1)和最后一次就诊(第 3 次就诊,Visit 3)报告其感知身体疲劳能力。感知身体疲劳能力使用自评的匹兹堡疲劳量表(PFS)的 10 项条目进行测量,评分为 0-50 分。采用两样本 t 检验比较干预组间第 3 次就诊与第 1 次就诊时感知身体疲劳能力的均值差异。

结果

在这项研究的 41 例女性(平均年龄 54.9±9.8 岁;80%为白人)中,按干预组划分,社会人口统计学、临床特征和基线疲劳水平相似,除使用抗雌激素药物外。运动干预组 PFS 躯体评分的干预后变化(平均 ∆±SE)为-4.4±1.4 分(-22.5%),对照组为 0.2±1.4 分(+1.0%)(p=0.022)。

结论

PFS 捕捉到了乳腺癌幸存者运动干预后疲劳的减轻。这些发现有助于通过引入更敏感的测量感知身体疲劳能力的工具来减轻肿瘤患者的疲劳感,从而为未来癌症试验中更好地评估患者报告的结局提供支持。

试验注册

Clinicaltrials.gov 标识符:NCT02770781。

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