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新冠病毒感染康复后患者的运动康复:不同训练方式的随机对照试验

Exercise rehabilitation in post COVID-19 patients: a randomized controlled trial of different training modalities.

作者信息

Sick Johanna, Steinbacher Verena, Kotnik Daniel, König Florian, Recking Tim, Bengsch Dominik, König Daniel

机构信息

Department of Sport and Human Movement Science, Center for Sport Science and University Sports, University of Vienna, Vienna, Austria -

Vienna Doctoral School of Pharmaceutical, Nutritional and Sport Sciences, University of Vienna, Vienna, Austria -

出版信息

Eur J Phys Rehabil Med. 2025 Feb;61(1):130-140. doi: 10.23736/S1973-9087.24.08487-9. Epub 2024 Dec 12.

DOI:10.23736/S1973-9087.24.08487-9
PMID:39665835
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11922198/
Abstract

BACKGROUND

Long-lasting symptoms (>12 weeks) following a COVID-19 infection are defined as the post-COVID-19 syndrome (PCS), often manifesting as fatigue and reduced exercise capacity. Thus, exercise has been suggested as a non-pharmacological therapy.

AIM

To investigate the effects of endurance vs. concurrent exercise on physical function, symptoms and quality of life in individuals with PCS, that did not need hospital admission during acute COVID-19.

DESIGN

Parallel-group, single-center, randomized controlled trial.

SETTING

This study was conducted at the University of Vienna.

POPULATION

Adult individuals with a SARS-CoV-2 infection at least 12 weeks prior to enrollment who reported at least one symptom specific to PCS and did not experience post-exertional malaise.

METHODS

Participants were randomized to either 12 weeks of supervised endurance training (ED) or concurrent training (CT), or a non-exercising control group (C). As the primary outcome, VO2peak was assessed pre and post intervention. Secondary outcomes were handgrip and lower body strength, heart rate variability, symptoms, health-related quality of life (HRQoL) and concentration performance. The main effects for time and group as well as the time*group interaction were assessed via a 2x2 analysis of variance. Additionally, within-group pre-post testing was performed.

RESULTS

Taking the study protocol into account, 42 subjects could be included in the analysis (N.=14 in each group). A significant time*group interaction favoring both exercise conditions was found for VO2peak (partial Eta=0.267; ED: +3.9 mL/min/kg; CT: +3.2 mL/min/kg). The Fatigue Severity Score significantly decreased in ED (Hedges' g=0.63) and CT (Hedges' g=0.82) from pre to post, but not in C. Breathlessness and lower body strength improved most in CT. Significant within-group improvements in HRQoL and the number of PCS symptoms occurred in all groups.

CONCLUSIONS

Both exercise regimes led to increases in VO2peak and lower fatigue scores in subjects with PCS. Improvements in HRQoL occurred in all groups, however more pronounced after the exercise interventions. No definite conclusion about the superiority of either training modality can be drawn.

CLINICAL REHABILITATION IMPACT

The results show that in this population both exercise regimes are feasible and safe and lead to improvements in various health domains.

摘要

背景

新冠病毒感染后持续存在超过12周的症状被定义为新冠后综合征(PCS),常表现为疲劳和运动能力下降。因此,运动被建议作为一种非药物治疗方法。

目的

研究耐力运动与同时进行的运动对新冠后综合征患者身体功能、症状和生活质量的影响,这些患者在新冠急性期无需住院治疗。

设计

平行组、单中心、随机对照试验。

地点

本研究在维也纳大学进行。

研究对象

入组前至少12周感染过严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的成年人,他们报告至少有一项新冠后综合征的特定症状,且未出现运动后不适。

方法

参与者被随机分为三组,分别进行为期12周的有监督的耐力训练(ED)、同时进行的训练(CT)或不运动的对照组(C)。作为主要结局指标,在干预前后评估最大摄氧量(VO₂peak)。次要结局指标包括握力和下肢力量、心率变异性、症状、健康相关生活质量(HRQoL)和注意力表现。通过2×2方差分析评估时间和组别的主要效应以及时间*组别交互作用。此外,还进行了组内干预前后的测试。

结果

考虑到研究方案,42名受试者可纳入分析(每组N = 14)。在最大摄氧量方面发现了显著的时间*组别交互作用,表明两种运动条件均有优势(偏η² = 0.267;耐力训练组:增加3.9 mL/min/kg;同时进行的训练组:增加3.2 mL/min/kg)。从干预前到干预后,耐力训练组(Hedges' g = 0.63)和同时进行的训练组(Hedges' g = 0.82)的疲劳严重程度评分显著降低,而对照组未降低。呼吸困难和下肢力量在同时进行的训练组中改善最为明显。所有组在健康相关生活质量和新冠后综合征症状数量方面均有显著的组内改善。

结论

两种运动方案均使新冠后综合征患者的最大摄氧量增加,疲劳评分降低。所有组的健康相关生活质量均有改善,但运动干预后更为明显。无法得出关于哪种训练方式更具优势的确切结论。

临床康复影响

结果表明,在该人群中,两种运动方案都是可行且安全的,并能在多个健康领域带来改善。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8480/11922198/bbf5082befe8/8487-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8480/11922198/af584d9c0188/8487-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8480/11922198/3ef30867d38c/8487-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8480/11922198/5ffee166d712/8487-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8480/11922198/bbf5082befe8/8487-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8480/11922198/af584d9c0188/8487-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8480/11922198/3ef30867d38c/8487-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8480/11922198/5ffee166d712/8487-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8480/11922198/bbf5082befe8/8487-f4.jpg

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