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临床试验/NCT03840330
NCT03840330已完成不适用

Effects of High-intensity Interval Circuit Training (HIICT) on the Cardiovascular and Functional Parameters of Aged Women

Universidad de Almeria0 个研究点目标入组 54 人开始时间: 2015年12月20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
54
主要终点
Analyses changes in maximum oxygen consumption (VO2max).

研究概览

简要总结

This study evaluates the adaptations on the functional capacity and cardiovascular in elderly after a physical activity program circuit training. The participants were divided into three groups: Circuit training based on high-intensity interval training group (HIICT), Circuit training at moderate intensity group (MICT) and Control group (CG).

详细描述

Three groups of participants (circuit training based on high-intensity interval training, circuit training at moderate intensity and not training group) will enter the study. The intervention will consist of a physical exercise program in day centers.

Intensity progression will be encouraged according to the rate of perceived exertion. Progression of exertion will be "very hard", "extremely hard" and "maximal exertion" for HIT group, and "light", "somewhat hard" and "hard" for group. Assessment will be undertaken at two-time points: baseline and after 16 weeks of exercise training.

Assessment will include VO2 peak, functional capacity, health-related quality of life, cognitive state and daily physical activity.

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
50 Years 至 90 Years(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Having 50 - 90 years old.
  • Not suffering chronic heart, respiratory or joint disease, taking medication or having a deteriorated level of mental health that could interfere in carrying out exercise programs.
  • Having 0 or 1 responses positive in the Physical Activity Readiness Questionnaire (ParQ). Only item 6, related to mild vascular diseases.
  • Being physically independent according to the scales Lawton and Brody, and Katz.

排除标准

  • Having uncontrolled arterial hypertension.
  • Having practiced during the previous 3 months or practicing at present a similar exercise to the one proposed in the study.
  • Attending sessions less than 80%.

研究组 & 干预措施

High-intensity interval training group

Experimental

Frequency: 2 days/weeks; Intensity: 16-18 Börg/85-100%VO2max; Recovery: Active; Duration: 1 hour.

干预措施: Experimental: High-intensity interval training group (Other)

Moderate-intensity interval training group

Experimental

Frequency: 2 days/weeks; Intensity: 12-14 Börg/60-70% VO2max; Recovery: Active; Duration: 1 hour.

干预措施: Experimental: Moderate-intensity interval training group (Other)

Control group

No Intervention

Maintain their normal daily activities throughout the sixteen-week experimental period.

结局指标

主要结局

Analyses changes in maximum oxygen consumption (VO2max).

时间窗: Pre and post after sixteen weeks of intervention

A modified Balke treadmill protocol will be used to estimate aerobic capacity (VO2max).

次要结局

  • Analyses changes in gait.(Pre and post after sixteen weeks of intervention.)
  • Analyses changes in blood pressure reached in ergometry.(Pre and post after sixteen weeks of intervention)
  • Analyses changes in maximum speed reached in ergometry.(Pre and post after sixteen weeks of intervention)
  • Analyses changes in body mass index (BMI).(Pre and post after sixteen weeks of intervention.)
  • Analyses changes in lower body strength.(Pre and post after sixteen weeks of intervention.)
  • Analyses changes in upper body strength.(Pre and post after sixteen weeks of intervention.)
  • Analyses changes in heart rate reached in ergometry.(Pre and post after sixteen weeks of intervention)
  • Analyses changes in duration test reached in ergometry.(Pre and post after sixteen weeks of intervention)
  • Analyses changes in fat percentage.(Pre and post after sixteen weeks of intervention.)
  • Analyses changes in balance.(Pre and post after sixteen weeks of intervention.)
  • Analyses changes in maximal handgrip strength.(Pre and post after sixteen weeks of intervention.)

研究者

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

María Carrasco Poyatos

Principal Investigator

Universidad de Almeria

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