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临床试验/NCT03557736
NCT03557736已完成不适用

Effects of a 12-Week Home-Based High-Intensity Interval Training Programme in Obese Individuals With Elevated Cardiovascular Disease Risk: A Pilot Study

Liverpool John Moores University1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2015年3月9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
32
试验地点
1
主要终点
change in aerobic fitness

研究概览

简要总结

This study aims to investigate the efficacy of a novel home-based high-intensity interval training (Home-HIT) intervention in obese individuals, with elevated cardiovascular disease (CVD) risk. It was hypothesised that Home-HIT would 1) have high adherence to the prescribed exercise intensity (compliance), 2) improve markers of CVD risk, and 3) lead to favourable skeletal muscle adaptations.

详细描述

The applicability of current high intensity interval training (HIT) protocols to the sedentary obese population has been disputed by public health experts. Existing HIT interventions have been successful only under optimal conditions with high levels of supervision and specialised equipment, creating further barriers to exercise in those most in need. We aimed to eliminate many of these barriers by modifying existing HIT protocols to create a new home-based HIT (Home-HIT) intervention tailored to individuals with low fitness and mobility. It was hypothesised that Home-HIT would 1) have high adherence to the prescribed exercise intensity (compliance) and 2) improve markers of cardiovascular disease (CVD) risk. 32 Obese adults with at least 3 additional CVD risk factors (age 36±2 y; BMI 34.3±0.8 kg∙m-2; VO2peak 24.6±1.0 ml∙kg∙min-1), completed one of three 12-week training programmes 3x/week: Home-HIT (n=9); Laboratory-based supervised HIT (Lab-HIT; n=10) or home-based moderate intensity continuous training (Home-MICT; n=13). Adherence and compliance were monitored online in almost "real time" using a heart rate (HR) monitor and mobile app. The Home-HIT group completed 4 progressing to 8 1min intervals interspersed with 1min of rest in an unsupervised place of their choosing. The intervals were composed of simple bodyweight exercises that required no equipment. Changes in VO2peak, insulin sensitivity, body composition, flow-mediated dilation (FMD) and aortic pulse wave velocity (PWV) were assessed. Muscle biopsies were taken to assess changes in capillarisation, mitochondrial density, intramuscular triglyceride (IMTG) content and eNOS and GLUT4 protein expression using quantitative immunofluorescence microscopy.

研究设计

研究类型
Interventional
分配方式
Non 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 55 Years(Adult)
性别
All
接受健康志愿者
否

入选标准

  • •obesity (BMI >30 kg/m2)
  • •age 18-55

排除标准

  • •diagnosed CVD and other contraindications to participate in an exercise intervention
  • •BMI <30 kg/m2

研究组 & 干预措施

Home-HIT

Experimental

Home-based high-intensity interval training: participants performed 12 weeks of simple body weight exercises in a place of their own choosing 3x/week

干预措施: Training mode (Behavioral)

Home-MICT

Experimental

Home-based moderate-intensity interval training: participants performed 12 weeks of continuous exercise (running, swimming or cycling) in a place of their own choosing 3x/week

干预措施: Training mode (Behavioral)

Lab-HIT

Experimental

Laboratory-based high-intensity interval training: participants performed supervised cycle exercise under laboratory conditions 3x/week for 12 weeks

干预措施: Training mode (Behavioral)

结局指标

主要结局

change in aerobic fitness

时间窗: change in baseline aerobic fitness at 12 weeks

change in maximal aerobic capacity following the training

Adherence and compliance to the exercise training intervention

时间窗: adherance and compliance to the training over the 12 weeks

Session completion rate (adherence) and ability to meet target heart rates (compliance)

次要结局

  • change in body fat percentage(chage in baseline body fat percentage at 12 weeks)
  • change in baseline FMD(change in baseline FMD at 12 weeks)
  • change in vascular stiffness(change in baseline vascular stiffness at 12 weeks)

研究者

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

Sam Shepherd

Dr Sam Shepherd

Liverpool John Moores University

研究点 (1)

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