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临床试验/NCT03743610
NCT03743610已完成不适用

Investigation of Physiological Adaptations to Simulated Intermittent Altitude on Human Health and Performance

Mayo Clinic1 个研究点 分布在 1 个国家目标入组 71 人开始时间: 2019年1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
发起方
Mayo Clinic
入组人数
71
试验地点
1
主要终点
Change in hemoglobin

研究概览

简要总结

The investigators expect to find that different intensity and altitude exposure levels will show what kind of intermittent exposure protocol is more beneficial to athletes and healthy individuals that experience acute exposure to altitude during exercise. This may furthermore be related to acute altitude exposure for recreational exercise use as well.

研究设计

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

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •18-70 years of age,
  • •history of good health,
  • •generally active to competitive athletes.

排除标准

  • •History of cardiac or pulmonary disease,
  • •not currently active,
  • •unable to exercise or meet study requirements (e.g., number of sessions),
  • •live at altitude (>2,100m or 7,000ft).

研究组 & 干预措施

Effect of heart rate training in simulated altitude

Experimental

Participants will exercise in simulated altitude start at a minimum of 2,000ft and will increase to no greater than 16,400ft with each visit. The increase will be in accordance to maintaining >65% max heart rate during room air based maximal peak work.

干预措施: Simulated altitude (Other)

Effect of saturation of oxygen training in simulated altitude

Experimental

Participants will exercise in simulated altitude start at a minimum of 2,000ft and will increase to no greater than 16,400ft with each visit. The increase will be in accordance to maintaining 40-60% of max work rate during room air work rate and based upon saturation of oxygen of between 70-80%.

干预措施: Simulated altitude (Other)

Effect of optimized training in simulated altitude

Active Comparator

Participants will perform the more beneficial intervention (heart rate or saturation of oxygen training) to evaluate whether it improves elite athlete's training status at altitude.

干预措施: Simulated altitude (Other)

Effect of placebo training in non-simulated altitude

Placebo Comparator

Participants will perform placebo beneficial intervention (heart rate or saturation of oxygen training) to evaluate whether the optimized protocol truely improves elite athlete's training status at altitude.

干预措施: Placebo simulated altitude (Other)

结局指标

主要结局

Change in hemoglobin

时间窗: Baseline, 2-week, 4-week, 6-week, and 8-week

Change in hematocrit

时间窗: Baseline, 2-week, 4-week, 6-week, and 8-week

Change in erythropoietin

时间窗: Baseline, 2-week, 4-week, 6-week, and 8-week

次要结局

  • Change in peak VO2(Baseline and 6- and 8-week)
  • Change in cycling performance at altitude(Baseline and 6- and 8-week)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Courtney M. Wheatley

Principal Investigator

Mayo Clinic

研究点 (1)

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