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临床试验/NCT03306069
NCT03306069已完成不适用

Low-volume Aerobic Interval Training in Overweight Individuals at Increased Cardiometabolic Risk: Impact of Training Intensity on Cardiorespiratory Fitness, Cardiometabolic Risk Profile and Exercise Adherence

University of Erlangen-Nürnberg Medical School2 个研究点 分布在 1 个国家目标入组 154 人开始时间: 2017年11月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
154
试验地点
2
主要终点
Cardiorespiratory Fitness (CRF)

研究概览

简要总结

The main purpose of this study is to compare the impact of aerobic interval training intensity on exercise adherence and changes in cardiorespiratory fitness, cardiometabolic risk profile, body composition, inflammatory markers and subjective health outcomes after a 12-week intervention trial in overweight individuals at increased cardiometabolic risk.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

盲法说明

Outcome Assessors involved in data analysis will not be aware of the arm to which the participants were allocated (single-blinded masking).

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

  • Body Mass Index >/=30
  • presence of at least 2 cardiometabolic risk factors

排除标准

  • Healthy persons or patients under age
  • Overweight persons without any additional cardiometabolic risk factors
  • Pregnancy, Lactation
  • Psychological disorders, epilepsy, sever neurological disorders
  • Participation in other exercise- or nutrition studies within the last 6 months
  • acute cardiovascular disease
  • malignant disease
  • Electronic implants (defibrillator, pacemaker)
  • Persons in mental hospitals by order of authorities or jurisdiction

结局指标

主要结局

Cardiorespiratory Fitness (CRF)

时间窗: 12 weeks (baseline to 12 week follow-up assessment)

CRF will be assessed by measuring Maximum Oxygen uptake (VO2max)

次要结局

  • Metabolic Syndrome Z-Score (MetS-Z-Score)(12 weeks (baseline to 12 week follow-up assessment))
  • Body Composition(12 weeks (baseline to 12 week follow-up assessment))
  • Insulin sensitivity(12 weeks (baseline to 12 week follow-up assessment))
  • Inflammation(12 weeks (baseline to 12 week follow-up assessment))
  • Health-related quality of life(12 weeks (baseline to 12 week follow-up assessment))
  • Pain scores(12 weeks (baseline to 12 week follow-up assessment))
  • Perceived stress(12 weeks (baseline to 12 week follow-up assessment))
  • Subjective work ability(12 weeks (baseline to 12 week follow-up assessment))

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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