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使用商业活动监测器在 COPD 肺康复中坚持步行运动处方:一项可行性试验。

Adherence to walking exercise prescription during pulmonary rehabilitation in COPD with a commercial activity monitor: a feasibility trial.

机构信息

CERS, University Hospitals of Leicester NHS Trust, Leicester, UK.

Pulmonary Rehabilitation Department, Glenfield Hospital, Groby Road, Leicester, LE3 9QP, UK.

出版信息

BMC Pulm Med. 2021 Jan 18;21(1):30. doi: 10.1186/s12890-021-01406-9.

Abstract

BACKGROUND

Regular exercise is important in the management of COPD. Pulmonary rehabilitation (PR) facilitates a more physically active lifestyle through exercise participation, ideally without compromising non-exercise physical activity (PA). During PR patients are advised to perform exercise defined by duration and intensity. The extent to which PR attendees participate in unsupervised exercise bouts and their adherence to the exercise prescription provided during PR is unclear. Commercially available devices have the potential to support patients to exercise at their individually prescribed intensity. Study aims were to (1) assess how adherent patients are to their prescribed walking intensity; (2) examine the pattern of overall PA and walking exercise during the course of PR; (3) determine the feasibility of prescribing exercise to PR attendees using an activity monitor; and (4) explore the relationship between exercise and non-exercise PA with routine PR outcome measures.

METHODS

19 patients wore an activity monitor during routine walking tests and 6 weeks of PR, recording in a diary when they exercised. Exercise intensity (cadence) was prescribed from the Endurance Shuttle Walk Test. Patients completed questionnaires, walking tests and a lower limb strength test before and after PR. Repeated ANOVA compared changes in outcomes between weeks 1-6.

RESULTS

Patients wore the monitor every day during PR (median 42 days). Exercise steps increased by 56% (Δ332 [95% CI 54-611] steps/day, p = 0.009) between weeks 1 and 6, with no significant change in non-exercise steps (Δ79 [95% CI - 22 to - 179] steps/day, p = 0.13). Patients reported exercising on 70% of days. Adherence to prescribed cadence was achieved 55% of time spent exercising, and did not change across the 6 weeks (p = 0.907). Change in total daily steps was associated with improved dyspnea (p = 0.027), Chronic Respiratory Questionnaire (CRQ) Dyspnea domain (p = 0.019), CRQ Emotional Functioning domain (p = 0.001) and CRQ Mastery domain scores (p = 0.001) but not with exercise capacity or lower limb muscle strength.

CONCLUSIONS

Improvements in exercise participation, not at the expense of non-exercise PA, throughout a PR course was observed in attendees provided with a commercially available activity monitor. Wearable technology may be able to support effective remote walking exercise prescription and participation during PR. Trial registration (retrospectively registered): http://www.isrctn.com/ISRCTN15892972 .

摘要

背景

规律运动对于 COPD 的管理非常重要。肺康复(PR)通过运动参与促进更积极的生活方式,理想情况下不会影响非运动体力活动(PA)。在 PR 期间,患者被建议按照持续时间和强度进行运动。PR 参与者参与无监督运动的程度以及他们对 PR 期间提供的运动处方的依从性尚不清楚。市售设备具有支持患者按照个人规定强度进行运动的潜力。研究目的是:(1)评估患者对规定步行强度的依从性;(2)检查 PR 期间整体 PA 和步行运动的模式;(3)确定使用活动监测器为 PR 参与者规定运动的可行性;(4)探索运动与非运动 PA 与常规 PR 结果测量之间的关系。

方法

19 名患者在常规步行测试和 6 周的 PR 期间佩戴活动监测器,并在日记中记录锻炼时间。运动强度(步频)是根据耐力穿梭步行测试规定的。患者在 PR 前后完成问卷调查、步行测试和下肢力量测试。重复方差分析比较第 1 周到第 6 周的结果变化。

结果

患者在 PR 期间每天佩戴监测器(中位数 42 天)。运动步数增加了 56%(Δ332 [95% CI 54-611] 步/天,p=0.009),第 1 周到第 6 周之间,非运动步数没有明显变化(Δ79 [95% CI -22 至-179] 步/天,p=0.13)。患者报告在 70%的日子里进行了锻炼。在锻炼期间,按照规定的步频进行运动的时间占 55%,并且在 6 周内没有变化(p=0.907)。总步数的变化与呼吸困难的改善相关(p=0.027)、慢性呼吸问卷(CRQ)呼吸困难域(p=0.019)、CRQ 情绪功能域(p=0.001)和 CRQ 掌握域评分(p=0.001),但与运动能力或下肢肌肉力量无关。

结论

为参与者提供市售活动监测器后,在 PR 课程中观察到参与者的运动参与度增加,而不会影响非运动 PA。可穿戴技术可以支持 PR 期间有效的远程步行运动处方和参与。试验注册(回顾性注册):http://www.isrctn.com/ISRCTN15892972

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0836/7812648/65c71d83082b/12890_2021_1406_Fig1_HTML.jpg

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