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临床试验/NCT05863039
NCT05863039已完成不适用

Resistance Training With Blood Flow Restriction for the Lower Extremity Muscles

University of Oklahoma2 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2022年11月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
8
试验地点
2
主要终点
Force

研究概览

简要总结

Blood flow restriction associated with resistance training is suggested to potentiate increases in muscular strength and hypertrophy. This study will compare the effects of resistance training associated with blood flow restriction with a regular resistance training program. Findings of this project will provide important information regarding a promising intervention to potentiate muscle performance.

详细描述

The purpose of this study is to determine alterations in motor unit behavior of the tibialis anterior muscles after a resistance exercise program associated with blood flow restriction. Our working hypothesis is that blood flow restriction to working muscles will induce greater changes in muscle activation, lean mass and muscle size compared with a training at same intensity without blood flow restriction.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Basic Science
盲法
None

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Exclusion Criteria:
  • presence of neurological diseases,
  • presence of metal implants or joint replacement
  • any restriction to perform physical activity
  • pregnancy

排除标准

  • presence of neurological diseases,
  • presence of metal implants or joint replacement
  • any restriction to perform physical activity
  • pregnancy

研究组 & 干预措施

Group 1

Experimental

Strength training associated with blood flow restriction

干预措施: Blood flow restriction (Other)

Group 2

Experimental

Conventional strength training using high loads

干预措施: Regular training type 1 (Other)

Group 3

Experimental

Conventional strength training using low loads

干预措施: Regular training type 2 (Other)

结局指标

主要结局

Force

时间窗: 10 sessions (up to 6 weeks)

Force of the lower leg muscles using a custom made ergometer

次要结局

  • Body composition(Start and end of the protocol)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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