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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01380639
Other study ID # BGL-Ga-6MGT-0810
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 2010
Est. completion date April 2011

Study information

Verified date April 2019
Source Klinikum Berchtesgadener Land der Schön-Kliniken
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to investigate the exercise capacity in COPD-patients performing a vibration training additional to a standard three-week rehabilitation program in comparison to patients performing merely a rehabilitation program.


Recruitment information / eligibility

Status Completed
Enrollment 72
Est. completion date April 2011
Est. primary completion date April 2011
Accepts healthy volunteers No
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Chronic obstructive pulmonary disease III/IV

Exclusion Criteria:

- Severe exacerbations in the last 4 weeks prior to begin of study (definition of exacerbation: symptoms on more than 3 days with a relevant change in drug therapy (cortisone, antibiotics))

- Severe disease other than COPD, that could influence the results of the study

- Abuse of alcohol or drugs

- Simultaneously participation in another study

- Tachypnea (>30/min)

- Severe exacerbation during rehabilitation

- Cardiac insufficiency (NYHA IV)

- Myocardial infarction during the last 6 weeks

- Mental-health problem

- Pregnancy

- Known HIV-infection

- Slipped disk

- Acute discopathy

- Acute thrombosis

- Implants in trained regions of the body (lower extremities)

- Acute inflammation of the locomotor system, active arthrosis or rheumatoid arthritis

- Acute tendinopathy in trained regions of the body

- Acute hernia

- Fresh fractures, wounds or scars in trained regions of the body

- Gallstones or stones in the urinary tract collection system

Study Design


Related Conditions & MeSH terms


Intervention

Other:
whole body vibration training
performing squats for 3x3 minutes while using vibration platform three times a week

Locations

Country Name City State
Germany Schön Klinikum Berchtesgadener Land Schönau am Königssee

Sponsors (1)

Lead Sponsor Collaborator
Klinikum Berchtesgadener Land der Schön-Kliniken

Country where clinical trial is conducted

Germany, 

Outcome

Type Measure Description Time frame Safety issue
Primary 6-Minute-Walking-Distance Change in 6-minute-walking-distance from baseline to day 19 day 1, day 19
Secondary Body Composition Change in body composition from baseline to day 19 day 1 and 19
Secondary Isometric Maximum Handgrip Force change in isometric max. handgrip force from baseline to day 19 day 1, day 19
Secondary BODE-Score Change in Bode-Score from baseline to day 19 day 1, day 19
Secondary Lung Function day 1
Secondary Arterial Blood Gas day 1
Secondary Brain Natruretic Peptide (BNP) change in BNP from baseline to day 19 day 1, day 19
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