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临床试验/NCT02209207
NCT02209207已完成不适用

Continuous Versus Interval Walking Training in Patients With Severe Chronic Obstructive Pulmonary Disease - a Pilot Study

Schön Klinik Berchtesgadener Land2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2014年7月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
20
试验地点
2
主要终点
perceived exertion for dyspnea during walking training

研究概览

简要总结

This study will investigate the effects of interval walking training versus continuous walking training in patients with chronic obstructive pulmonary disease. Patients will be recruited during a 3-week inpatient pulmonary rehabilitation program and will be randomized to one of the two intervention groups. All walking training sessions will be performed on the same treadmill. Walking intensity in the continuous walking group will be 60 percent of the average speed of the 6-minute walking test. Patients in the interval training group will perform high intensity intervals at 120% of the 6-minute walking test speed for 60 seconds alternating with 60 seconds of rest. The total exercise duration will be progressively increased from 10 to 32 minutes.

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)

入排标准

性别
All
接受健康志愿者

入选标准

  • COPD stage III or IV according to the Global Initiative for chronic obstructive lung disease [GOLD]
  • stationary patient in the Schön Klinik Berchtesgadener Land

排除标准

  • acute, severe exacerbation of COPD
  • failure to comply with study process

结局指标

主要结局

perceived exertion for dyspnea during walking training

时间窗: day 1 to 21

measured via modified Borg scale (0 to 10)

次要结局

  • 6-minute walking test(day 1 to 21)
  • heart rate during walking training(day 1 to 21)
  • Oxygen saturation during walking training(day 1 to 21)
  • perceived exertion for leg fatigue (Borg-scale)(during three weeks of rehabilitation)
  • Sit-to-stand-test(day 1 to 21)
  • fat free mass in kilogram(day 1 to 21)
  • forced expiratory volume in 1 second (FEV1) in liter(day 1 to 21)
  • 36 item short-form health Survey (SF-36)(day 1 to 21)
  • chronic respiratory questionnaire (CRQ)(day 1 to 21)
  • hospital anxiety and depression scale (HADS)(day 1 to 21)

研究者

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

Klaus Kenn

Head physican (department of pneumology)

Schön Klinik Berchtesgadener Land

研究点 (2)

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