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临床试验/NCT04065191
NCT04065191Unknown不适用

High-intensity Interval Training for Workplace Health Promotion: Evaluation of Feasibility and Preventive Effects in a Real-World Setting

University of Erlangen-Nürnberg Medical School2 个研究点 分布在 1 个国家目标入组 300 人开始时间: 2019年5月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
发起方
入组人数
300
试验地点
2
主要终点
Cardiorespiratory Fitness (CRF)

研究概览

简要总结

The aim of this study is to investigate the effects of an extremely time-efficient high-intensity interval training program, performed over a period of six months in a real-world (workplace) setting, on cardiorespiratory fitness, cardiometabolic risk profile, and self-reported outcomes including perceived stress and subjective work ability in previously sedentary employees.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Sedentary Lifestyle over at least 1 year prior to the study

排除标准

  • Pregnancy, Lactation
  • Psychological disorders, epilepsy, sever neurological disorders
  • Participation in other exercise- or nutrition studies within the last 6 months
  • coronary heart disease, heart failure
  • malignant disease
  • severe rheumatic or neurological disease
  • severe/unstable hypertension (resting RR: >180/>110 mmHg)
  • severely restricted lung function (FEV1 <60%)
  • unstable Diabetes mellitus
  • severe orthopedic disease/restriction
  • acute / chronic infectious diseases
  • Electronic implants (defibrillator, pacemaker)
  • Persons in mental hospitals by order of authorities or jurisdiction

研究组 & 干预措施

High-intensity interval training

Experimental

High-intensity interval training

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

结局指标

主要结局

Cardiorespiratory Fitness (CRF)

时间窗: 12 months [Change from Baseline to 6 months and Change from Baseline to 6 months after the end of the intervention]

CRF will be assessed by measuring maximum oxygen uptake (VO2max)

次要结局

  • Muscle mass(12 months [Change from Baseline to 6 months and Change from baseline to 6 months after the end of the intervention])
  • Insulin sensitivity(12 months [Change from Baseline to 6 months and Change from Baseline to 6 months after the end of the intervention])
  • Inflammation status(12 months [Change from Baseline to 6 months and Change from Baseline to 6 months after the end of the intervention])
  • Total body water(12 months [Change from baseline to 6 months and change from baseline to 6 months after the end of the intervention])
  • Metabolic Syndrome Z-Score (MetS-Z-Score)(12 months [Change from Baseline to 6 months and Change from Baseline to 6 months after the end of the intervention])
  • Fat mass(12 months [Change from baseline to 6 months and change from baseline to 6 months after the end of the intervention])
  • Pain scores(12 months [Change from Baseline to 6 months and Change from Baseline to 6 months after the end of the intervention])
  • Perceived stress(12 months [Change from Baseline to 6 months and Change from Baseline to 6 months after the end of the intervention])
  • Subjective work ability(12 months [Change from Baseline to 6 months and Change from Baseline to 6 months after the end of the intervention])
  • Health-related quality of life(12 months [Change from Baseline to 6 months and Change from Baseline to 6 months after the end of the intervention])

研究者

发起方
University of Erlangen-Nürnberg Medical School
申办方类型
Other
责任方
Sponsor

研究点 (2)

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