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Clinical Trials/NCT02209207
NCT02209207
Completed
Not Applicable

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

Schön Klinik Berchtesgadener Land1 site in 1 country20 target enrollmentJuly 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Obstructive Airway Disease
Sponsor
Schön Klinik Berchtesgadener Land
Enrollment
20
Locations
1
Primary Endpoint
perceived exertion for dyspnea during walking training
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

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.

Registry
clinicaltrials.gov
Start Date
July 2014
End Date
November 2015
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Klaus Kenn

Head physican (department of pneumology)

Schön Klinik Berchtesgadener Land

Eligibility Criteria

Inclusion Criteria

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

Exclusion Criteria

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

Outcomes

Primary Outcomes

perceived exertion for dyspnea during walking training

Time Frame: day 1 to 21

measured via modified Borg scale (0 to 10)

Secondary Outcomes

  • 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)

Study Sites (1)

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