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Swiss Study On Pulmonary Rehabilitation after Exacerbation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN84612310
Enrollment
280
Registered
2006-10-30
Start date
2006-09-11
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Chronic obstructive pulmonary disease Respiratory Chronic obstructive pulmonary disease

Interventions

Respiratory rehabilitation with supervised physical exercise for 12 weeks and patient education program "Living well with COPD" (identical for both treatment arms).

Sponsors

University Hospital of Zurich (Switzerland)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients after in- or outpatient treatment of acute exacerbation of COPD defined as a sustained worsening over days to weeks of the patient?s symptoms from his or her usual stable state that is beyond normal day-to-day variations and the presence of at least two of the following symptoms: 1.1. Breathlessness 1.2. Cough 1.3. Increased sputum production, and 1.4. Change in sputum colour 2. At least two exacerbations in previous two years requiring in- or outpatient care 3. Within last three years, during stable phase, documented COPD with Gold stage II to IV 4. The patient is after in- or outpatient treatment in a medical condition that allows an immediate respiratory rehabilitation or recovery at home 5. More than 40 years of age

Exclusion criteria

Exclusion criteria: 1. Hospitalisation for other reasons than acute exacerbation of COPD 2. Long term non-invasive ventilation (all but continuous positive airway pressure [CPAP], which is allowed) 3. Other lung diseases: Doctor diagnosed asthma and/or more than 20% reversibility of airflow obstruction after beta-2-mimetika during stable phase of COPD 4. Patients who cannot be randomised to usual care for medical reasons: 4.1. Impaired level of consciousness 4.2. Acute confusion 4.3. Acute changes on the radiograph or electrocardiogram 4.4. Arterial pH less than 7.35, or 4.5. Concomitant medical conditions 5. Orthopaedic, rheumatologic, cardiovascular or neurological disorders that inhibit exercise training, gymnastic or guided walking tours 6. Inability to follow patient education due to language (no German, French or Italian as communication language) or mental disorders (e.g. substance abuse, psychosis, dementia)

Design outcomes

Primary

MeasureTime frame
Exacerbations requiring medical care (in- or outpatient).

Secondary

MeasureTime frame
1. Health-related quality of life (Chronic Respiratory Questionnaire and Feeling Thermometer) 2. Dyspnea (Medical Research Council scale) 3. Mortality 4. Costs

Countries

Switzerland

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Apr 3, 2026