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临床试验/NCT02498223
NCT02498223Unknown不适用

Adjusting the Load Carried by the Soldier According to Body Composition Measurements and Aerobic Capacity

Sheba Medical Center2 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2015年9月最近更新:
适应症
干预措施

试验速览

阶段
不适用
入组人数
50
试验地点
2
主要终点
oxygen consumption

研究概览

简要总结

In order to reduce the physiological and biomechanical loads that the soldiers are exposed to, the investigators want to examine new approaches for distributing the carried loads according to measurements that are specific for each soldier (body composition and aerobic capacity). A functional index (LCI=load carriage index) will provide the commander a tool for better decisions in distributing the same total load among the same number of soldiers, according to each soldier's ability.

详细描述

50 healthy, male and female combat soldiers will be recruited. Anthropometry and maximal aerobic capacity will be measured for each participant: Physiological evaluation: the participants will perform physical stress on a treadmill with changing slope and speed, once carrying 40% of their body weight (as the current instructions) and a second time with weight that is calculated by the examined body composition and aerobic capacity based index (LCI). The physiological response will be assessed based on heart rate, lactic acid in the blood and oxygen consumption.

Biomechanical evaluation: the biomechanical response will be measured in the biomechanical lab: pressure on the shoulder and waist from the load and straps, walk analysis and stress scatter in the foot.

By this experiment the investigators want to examine if the new index, the LCI, is physiologically and biomechanically better than the current load distribution instructions.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 25 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Aged 18-25 years.
  • Healthy soldiers volunteers.
  • Without heart, cardiovascular, metabolic or respiratory illnesses.
  • Without known medical illness or medication use that might endanger the participants.

排除标准

  • existence of any of undesired conditions detailed in the inclusion criteria.
  • the physician decision.

研究组 & 干预措施

research arm

Experimental

50 subjects (healthy soldiers, male and female) from combat units will undergo the experiment protocol.

干预措施: experiment protocol (Other)

结局指标

主要结局

oxygen consumption

时间窗: 3 experiment days

oxygen consumption will be monitored continuously through the experimental days by a metabolic system (ERGOTEST 680, ZAN, GERMANY )

次要结局

  • Heart rate(3 experiment days)
  • pressure at the shoulders and the waist(3 experiment days)
  • walk analysis (composite)(3 experiment days)

研究者

申办方类型
Other Gov
责任方
Sponsor

研究点 (2)

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