此页面是自动翻译的,不保证翻译的准确性。请参阅 英文版 对于源文本。

Effects of Combined Interventions to Optimize Recovery During High-intensity Exercises in Healthy Adults

2021年6月30日 更新者:Swiss Federal Institute of Technology
The objective of the study is to evaluate the effects a complex recovery intervention during the breaks of a repeated sprint test on exercise performance compared to placebo and control conditions. The enhanced recovery package (ERP) includes neck cooling with an iced gel pad, drinking a 6% CHO solution, mouth-rinsing with a 10% CHO, 6 mg・kg -1 caffeine solution, performing submaximal squats and hyperventilating a hyperoxic mixture; all applied in each 3-min break in-between the six 30-s sprints. This intervention will be compared to a placebo and a control condition.

研究概览

地位

完全的

条件

研究类型

介入性

注册 (实际的)

16

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

    • ZH
      • Zürich、ZH、瑞士、8057
        • ETH Zürich, Exercise Physiology Lab

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 40年 (成人)

接受健康志愿者

是的

有资格学习的性别

男性

描述

Inclusion Criteria:

  • Informed Consent as documented by signature (Appendix Informed Consent Form)
  • Healthy
  • Male
  • Age: 18-40 years
  • Body-Mass-Index (BMI): 18.5-24.9 kg・m-2
  • Trained individuals: max. Power output ≥ 4.0 Watts・kg-1
  • Non-smoking
  • Willingness to adhere to the study rules

Exclusion Criteria:

  • Known or suspected non-compliance, drug or alcohol abuse
  • Inability to follow the procedures of the study, e.g. due to language problems, psychological disorders, dementia, etc. of the participants
  • Previous enrolment into the current study
  • Intake of medications affecting performance or the respiratory, cardiovascular or neuromuscular system
  • Acute or chronic illness affecting performance or the respiratory, cardiovascular or neuromuscular system

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:其他
  • 分配:随机化
  • 介入模型:交叉作业
  • 屏蔽:单身的

武器和干预

参与者组/臂
干预/治疗
实验性的:ERP Intervention
Combination of different methods to improve recovery.

The ERP intervention is applied in a randomized and counter-balanced order across visits 2-4 in each 3-min break in-between the six 30-s sprints, with one intervention per visit. The order and timing of the constituents of the interventions will be strictly constant within and between participants.

ERP: 1) neck cooling with an iced gel pad, 2) drinking a ∼ 6% CHO solution, 3) mouth-rinsing with a ∼10% CHO, ∼6 mg ・ kg -1 caffeine solution, 4) performing submaximal squats and 5) hyperventilating a hyperoxic mixture

无干预:Control
Passive recovery by sitting on a chair
安慰剂比较:Placebo
A combination of methods similar to the ERP intervention but at an intensity / mixture supposed to be ineffective at improving recovery.

The control intervention is applied in a randomized and counter-balanced order across visits 2-4 in each 3-min break in-between the six 30-s sprints, with one intervention per visit. The order and timing of the constituents of the interventions will be strictly constant within and between participants.

1) neck "cooling" with room temperature gel pack, 2) drinking an artificially sweetened solution, 3) mouth-rinsing with artificially sweetened solution (containing no caffeine), 4) performing unloaded squat manoeuvres, 5) deep breaths with room air

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Change in mean power output
大体时间:through study completion, an expected average of 3 weeks per participant
Measured over the six 30s high-intensity cycling sprints in each of the three conditions. Mean power mirrors the body's ability to generate muscle power and physical energy. Any meaningful effects of the recovery interventions will eventually translate into a higher power output.
through study completion, an expected average of 3 weeks per participant
Change in fatigue index
大体时间:through study completion, an expected average of 3 weeks per participant
Fatigue index = drop in power output from the beginning to the end a 30s sprint test. The change in this index will be calculated from the 1st to the 6th sprint test in each condition.
through study completion, an expected average of 3 weeks per participant

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 首席研究员:Christina M. Spengler, Prof.、Christina M. Spengler, Prof. Study Principal Investigator Exercise Physiology Lab, Institute of Human Movement Sciences and Sport, ETH Zurich

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2020年9月10日

初级完成 (实际的)

2021年6月30日

研究完成 (实际的)

2021年6月30日

研究注册日期

首次提交

2020年8月4日

首先提交符合 QC 标准的

2020年8月7日

首次发布 (实际的)

2020年8月11日

研究记录更新

最后更新发布 (实际的)

2021年7月2日

上次提交的符合 QC 标准的更新

2021年6月30日

最后验证

2020年10月1日

更多信息

与本研究相关的术语

其他研究编号

  • ERP_2020

药物和器械信息、研究文件

研究美国 FDA 监管的药品

研究美国 FDA 监管的设备产品

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

ERP的临床试验

3
订阅