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临床试验/NCT03094689
NCT03094689Unknown不适用

Cold Water Immersion in the Recovery of Clinical, Biochemical, Functional and Neuromuscular Markers of Muscle Damage of 10km Street Runners: Clinical, Randomized and Blinded Trial

Universidade Federal do Rio Grande do Norte0 个研究点目标入组 30 人开始时间: 2017年1月最近更新:
适应症

试验速览

阶段
不适用
入组人数
30
主要终点
Subjective perception of pain.

研究概览

简要总结

Objective: To analyze the effect of cold water immersion (CWI) on the recovery of clinical, biochemical, functional and neuromuscular markers of muscle damage in 10 km street runners.

Materials and Methods: This is a randomized, blinded trial in which 30 subjects, 10 km street runners, were randomly divided into three groups: control (gC), immersion (gI) and CWI (gCWI). The runners will be evaluated for clinical (subjective perception of exertion), biochemical (serum CK), functional (unipodal triple hop distance and shuttle test time) and neuromuscular variables by means of isokinetic variables (peak torque, total work and fatigue index). Volunteers will perform pre-assessment, immediately post-race and post-intervention, and 24-hour post-intervention. The data will be expressed by mean and standard deviation, analyzed in the statistical package SPSS 20.0. A significance level of 5% and a 95% confidence interval will be considered for all measures.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Investigator)

入排标准

年龄范围
20 Years 至 40 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Body Mass Index between 18.5 and 30 kg/m2;
  • Street runners for at least 6 months;
  • Week frequency of at least 3 times;
  • Do not present cardiopathies, muscles and neurological diseases;

排除标准

  • Hypersensitivity or allergies to cryotherapy;
  • Unable to complete the 10 km event on the day of the evaluation;
  • Do not complete or perform any of the study procedures for any reason (phobias, do not withstand the exposure time).

结局指标

主要结局

Subjective perception of pain.

时间窗: Up to 10 weeks

The subjective perception of pain will be measured by means of the visual analogic scale based on the self-report of the level of pain.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Wouber Hérickson de Brito Vieira

Principal Investigator, Clinical Professor

Universidade Federal do Rio Grande do Norte

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