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萨尔茨堡10/7高强度间歇训练冲击周期研究:一项针对耐力训练运动员的随机对照试验的研究方案,该研究探讨了为期7天的高强度间歇训练冲击微周期(有无额外低强度训练)对耐力表现、幸福感、压力和恢复的影响。

The Salzburg 10/7 HIIT shock cycle study: the effects of a 7-day high-intensity interval training shock microcycle with or without additional low-intensity training on endurance performance, well-being, stress and recovery in endurance trained athletes-study protocol of a randomized controlled trial.

作者信息

Stöggl Thomas Leonhard, Blumkaitis Julia C, Strepp Tilmann, Sareban Mahdi, Simon Perikles, Neuberger Elmo W I, Finkenzeller Thomas, Nunes Natalia, Aglas Lorenz, Haller Nils

机构信息

Department of Sport and Exercise Science, University of Salzburg, Salzburg, Austria.

Red Bull Athlete Performance Center, Salzburg, Austria.

出版信息

BMC Sports Sci Med Rehabil. 2022 May 7;14(1):84. doi: 10.1186/s13102-022-00456-8.

Abstract

BACKGROUND

Performing multiple high-intensity interval training (HIIT) sessions in a compressed period of time (approximately 7-14 days) is called a HIIT shock microcycle (SM) and promises a rapid increase in endurance performance. However, the efficacy of HIIT-SM, as well as knowledge about optimal training volumes during a SM in the endurance-trained population have not been adequately investigated. This study aims to examine the effects of two different types of HIIT-SM (with or without additional low-intensity training (LIT)) compared to a control group (CG) on key endurance performance variables. Moreover, participants are closely monitored for stress, fatigue, recovery, and sleep before, during and after the intervention using innovative biomarkers, questionnaires, and wearable devices.

METHODS

This is a study protocol of a randomized controlled trial that includes the results of a pilot participant. Thirty-six endurance trained athletes will be recruited and randomly assigned to either a HIIT-SM (HSM) group, HIIT-SM with additional LIT (HSM + LIT) group or a CG. All participants will be monitored before (9 days), during (7 days), and after (14 days) a 7-day intervention, for a total of 30 days. Participants in both intervention groups will complete 10 HIIT sessions over 7 consecutive days, with an additional 30 min of LIT in the HSM + LIT group. HIIT sessions consist of aerobic HIIT, i.e., 5 × 4 min at 90-95% of maximal heart rate interspersed by recovery periods of 2.5 min. To determine the effects of the intervention, physiological exercise testing, and a 5 km time trial will be conducted before and after the intervention.

RESULTS

The feasibility study indicates good adherence and performance improvement of the pilot participant. Load monitoring tools, i.e., biomarkers and questionnaires showed increased values during the intervention period, indicating sensitive variables.

CONCLUSION

This study will be the first to examine the effects of different total training volumes of HIIT-SM, especially the combination of LIT and HIIT in the HSM + LIT group. In addition, different assessments to monitor the athletes' load during such an exhaustive training period will allow the identification of load monitoring tools such as innovative biomarkers, questionnaires, and wearable technology.

TRIAL REGISTRATION

clinicaltrials.gov, NCT05067426. Registered 05 October 2021-Retrospectively registered, https://clinicaltrials.gov/ct2/show/NCT05067426 . Protocol Version Issue date: 1 Dec 2021. Original protocol. Authors: TLS, NH.

摘要

背景

在一段较短的时间内(约7 - 14天)进行多次高强度间歇训练(HIIT)被称为HIIT冲击微周期(SM),有望使耐力表现迅速提高。然而,HIIT - SM的效果以及耐力训练人群在一个SM期间的最佳训练量相关知识尚未得到充分研究。本研究旨在考察两种不同类型的HIIT - SM(有或无额外低强度训练(LIT))与对照组(CG)相比,对关键耐力表现变量的影响。此外,在干预前、干预期间和干预后,使用创新生物标志物、问卷和可穿戴设备对参与者的压力、疲劳、恢复和睡眠进行密切监测。

方法

这是一项随机对照试验的研究方案,其中包括一名试点参与者的结果。将招募36名耐力训练运动员,并随机分配到HIIT - SM(HSM)组、有额外LIT的HIIT - SM(HSM + LIT)组或CG组。所有参与者将在为期7天的干预前(9天)、干预期间(7天)和干预后(14天)接受监测,共30天。两个干预组的参与者将在连续7天内完成10次HIIT训练,HSM + LIT组还将额外进行30分钟的LIT。HIIT训练包括有氧HIIT,即5次×4分钟,心率达到最大心率的90 - 95%,中间穿插2.5分钟的恢复期。为了确定干预效果,将在干预前后进行生理运动测试和5公里计时赛。

结果

可行性研究表明试点参与者的依从性良好且表现有所改善。负荷监测工具,即生物标志物和问卷显示在干预期内数值增加,表明这些变量具有敏感性。

结论

本研究将首次考察不同总训练量的HIIT - SM的效果,特别是HSM + LIT组中LIT和HIIT的组合。此外,在如此高强度的训练期间,通过不同的评估来监测运动员的负荷,将有助于识别负荷监测工具,如创新生物标志物、问卷和可穿戴技术。

试验注册

clinicaltrials.gov,NCT05067426。2021年10月5日注册 - 追溯注册,https://clinicaltrials.gov/ct2/show/NCT05067426 。方案版本发布日期:2021年12月1日。原始方案。作者:TLS,NH。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/092d/9077880/26226ea7ad93/13102_2022_456_Fig1_HTML.jpg

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