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Effectiveness of pulmonary rehabilitation: The role of interval and continuous endurance exercise training, lower and upper extremity strengthening and other intervention modalities

Subjective and objective outcomes in patients with COPD after pulmonary rehabilitation - The impact of comorbidities

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN14648515
Enrollment
32
Registered
2018-02-15
Start date
2013-03-01
Completion date
Unknown
Last updated
2020-12-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Comorbidities in chronic obstructive pulmonary disease. Respiratory Chronic obstructive pulmonary disease

Interventions

Participants are allocated to one of two groups, according to the presence or the absence of comorbidities. Patients with none or only one comorbidity (n=11, Group 1) are compared to those who have tw

Sponsors

Exercise Physiology Laboratory
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. COPD diagnosis of any stage (A, B, C, D) 2. Aged 49-76 years 3. Stable condition 4. Optimal bronchodilation therapy 5. Optimal therapy of comorbidities 6. Reduced exercise capacity 7. Full compliance to the rehabilition program and recommendations

Exclusion criteria

Exclusion criteria: 1. Active or unstable cardiovascular disease (within three months: myocardial infarction, severe uncontrolled arrhythmia, symptomatic or unstable cardiovascular disease, severe heart valve disease or severe heart failure) 2. Pulmonary embolism in the last three months 3. Ischemic cardiovascular stroke or hemorrhagic stroke in the last three months 4. Non-controlled arterial hypertension 5. Large abdominal aortic aneurysm 6. Severe orthopaedic disorders 7. Severe osteoporosis 8. Any condition that does not allow the performance of aerobic exercise 9. Severe dementia 10. Severe untreated psychiatric conditions 11. Unwilling, undisciplined patient who does not comply with medical recommendations

Design outcomes

Primary

MeasureTime frame
1. Arterial blood gases are measured and analysed using the GEM premier 3500 blood gas analyser at baseline and after 13 weeks 2. Pulmonary function is measured using Pulmonary Function Tests (spirometry, diffusing capacity and static lung volume) at baseline and after 13 weeks 3. Dyspnea is assessed using the modified Medical research Council (MRC) scale and the COPD Assessment Test at baseline and after 13 weeks 4. Quality of Life is assessed by the St George Respiratory Questionnaire (SGRQ) at baseline and after 13 weeks

Secondary

MeasureTime frame
1. Expiratory oxygen and carbon dioxide fractions are measured using the six minute walking test (6MWT) and standard cardiopulmonary exercise test at baseline and after 13 weeks 2. Work rate is measured using the six minute walking test (6MWT) and standard cardiopulmonary exercise test at baseline and after 13 weeks 4. Airflow is measured using the six minute walking test (6MWT) and standard cardiopulmonary exercise test at baseline and after 13 weeks 5. Cardiac frequency is measured using the six minute walking test (6MWT) and standard cardiopulmonary exercise test at baseline and after 13 weeks 6. Oxygen saturation is measured using the six minute walking test (6MWT) and standard cardiopulmonary exercise test at baseline and after 13 weeks

Countries

Greece

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 21, 2026