Long Term Physical Training in Asthma

This study has been completed.
Sponsor:
Information provided by:
Universitätsklinikum Hamburg-Eppendorf
ClinicalTrials.gov Identifier:
NCT01097473
First received: March 31, 2010
Last updated: NA
Last verified: March 2010
History: No changes posted

March 31, 2010
March 31, 2010
April 1996
January 1998   (final data collection date for primary outcome measure)
Maximum oxygen uptake [ Time Frame: One year ] [ Designated as safety issue: No ]
Maximum oxygen uptake measured during unsteady state cycle ergometer test with work increments of 10 watts each minute until exhaustion.
Same as current
No Changes Posted
  • General quality of life [ Time Frame: One year ] [ Designated as safety issue: No ]
    Assessment of general quality of life using the german version of the SF-36 questionaire.
  • Disease-specific quality of life [ Time Frame: One year ] [ Designated as safety issue: No ]
    Assessment of the disease-specific quality of life using the Asthma Quality of Life Questionnaire (AQLQ)
Same as current
Not Provided
Not Provided
 
Long Term Physical Training in Asthma
Effects of Long Term Physical Training Once a Week on Fitness and Quality of Life in Elderly Asthmatics

This controlled study is undertaken to investigate the effects of a long term outpatient training program on physical fitness and quality of life in elderly asthmatics.

Physical training is well known to support a healthy lifestyle. Patients with asthma are often unnecessarily restricted of physical activities or avoid exercise due to the unpleasant experience of exercise-induced dyspnea. As a consequence both children and adults with asthma are less fit than their peers. Like in healthy individuals, regular training supports health in asthmatics. In short-term training programs improvements of physical capabilities have been achieved in children and young adults with asthma. Programs of longer durations than 3 months have not been published in controlled trials. Effects of exercise training on quality of life in adult asthmatics are lacking.

Interventional
Not Provided
Allocation: Non-Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Single Blind (Outcomes Assessor)
Primary Purpose: Treatment
Asthma
Procedure: Exercise training
Exercise training in outpatient sport groups once weekly with a duration of 60 min each
  • Active Comparator: Exercise training
    Subjects participate in a once weekly supervised exercise training group, duration of 60 min.
    Intervention: Procedure: Exercise training
  • No Intervention: Control
    Control group receives no intervention
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
24
March 1998
January 1998   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • physician diagnosed asthma
  • non-smoker
  • stable condition
  • informed consent

Exclusion Criteria:

  • participation in pulmonary rehabilitation in the past 12 months prior to study inclusion
  • unability to attend training sessions on a regular basis for one year
  • symptomatic coronary heart disease
  • uncontrolled heart failure
  • hemodynamically relevant cardiac rhythm disorders
  • hemodynamically relevant cardiac valvular disorders
  • uncontrolled arterial hypertension
  • hypercapnic respiratory failure
  • severe hypoxemia (i.e. PaO2 <50 mm Hg resp. SaO2 <80% at rest)
  • history of decompensated right heart failure
  • pulmonary arterial hypertension (PA mean pressure at rest >20 mm Hg)
  • severe osteoporosis
  • severe airway obstruction (FEV1 <50% predicted, FEV1 <60% predicted following bronchodilatation)
  • maximum work rate of less than 50 watt during ergometer testing
  • uncontrolled asthma
  • COPD exacerbation
  • severe adipositas (BMI >35 kg/m2)
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
Germany
 
NCT01097473
AM-001
No
Andreas Meyer, Krankenhaus St. Kamillus, Mönchengladbach, Germany
Universitätsklinikum Hamburg-Eppendorf
Not Provided
Principal Investigator: Andreas Meyer, M.D. Kliniken Mariahilf GmbH, Mönchengladbach, Germany
Universitätsklinikum Hamburg-Eppendorf
March 2010

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP