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临床试验/NCT03940261
NCT03940261已完成不适用

Physiological Benefits of High-intensity Interval Training for Individuals With Parkinson's Disease

University of Guelph2 个研究点 分布在 1 个国家目标入组 28 人开始时间: 2019年6月12日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
28
试验地点
2
主要终点
Maximal exercise capacity

研究概览

简要总结

Aerobic exercise is recommended for individuals with Parkinson's disease (PD) and can improve quality of life, both physically and mentally. The most efficacious program to achieve these exercise benefits is unknown. Recently, high-intensity interval training (HIIT) has been shown to be safe and more effective in many high-risk populations with limited exercise tolerance. Shorter bouts of exercise are likely better tolerated in PD due to difficulty sustaining muscle contractions. The goal of this project is to determine whether HIIT produces superior cardiorespiratory, neuromuscular, biomechanical, and clinical adaptations than conventional continuous moderate intensity training (CMIT) in PD.

详细描述

The specific research aims are to compare, in PD, the effects of HIIT or CMIT on: 1) maximal exercise capacity; 2) neural and non-neural factors contributing to muscle strength, power and fatigability; 3) biomechanical measures of postural stability and gait; and 4) Clinical markers (Mini-BESTest and Unified Parkinson's Disease Rating Scale (UPDRS)). The investigators hypothesize that, HIIT will produce greater improvements in: 1) exercise capacity; 2) muscle strength, power and reduced fatigability; 3) stability and gait velocity; and 4) clinical markers.

Methods: This pilot project will involve a randomized trial of 30 individuals with PD comparing the effects of HIIT and CMIT. Training will be completed thrice weekly for 10 weeks. Participants will include men and women between 50-85 years of age, who are able to stand unsupported for 1 min, walk 18m without use of an aid, and mount a stationary bike. Participants will be randomized to either HIIT (10, 1-minute cycling intervals at 90% of peak power output, each separated by 1-min at 10% peak power output) or CMIT (30-50min cycling at 60% of peak power output). Participants will undergo the following pre- and post-training assessments: Cardiovascular testing will examine hemodynamic and efferent muscle sympathetic responses to static handgrip exercise and post-exercise circulatory occlusion; Neuromuscular testing will examine muscle activity (electromyography) during voluntary and electrically stimulated contractions of the knee extensors; Biomechanical testing will examine whole-body stability, gait, and balance patterns; and Clinical risk assessments (Mini-BESTest and UPDRS).

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

The collection of study outcomes will be completed by individuals blinded to group allocation.

入排标准

年龄范围
45 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Men and women between 45-85 years of age
  • Clinical diagnosis of Parkinson disease
  • Able to stand unsupported for 1 minute
  • Able to walk 18 metres without aid
  • Able to mount a stationary bike

排除标准

  • History of dementia
  • History of stroke
  • Type 1 diabetes
  • Autonomic neuropathy
  • Currently involved in formal exercise training (>3 day per week).

结局指标

主要结局

Maximal exercise capacity

时间窗: Change from baseline following 10 weeks of aerobic exercise training

VO2 max

次要结局

  • Handgrip strength(Change from baseline following 10 weeks of aerobic exercise training)
  • Blood Pressure(Change from baseline following 10 weeks of aerobic exercise training)
  • Mini-Balance Evaluation Systems Test (Mini-BESTest)(Change from baseline following 10 weeks of aerobic exercise training)
  • Unified Parkinson's Disease Rating Scale (UPDRS)(Change from baseline following 10 weeks of aerobic exercise training)
  • Heart Rate(Change from baseline following 10 weeks of aerobic exercise training)

研究者

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

Philip Millar

Assistant Professor

University of Guelph

研究点 (2)

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