Chronic Obstructive Pulmonary Disease and Pulmonary Rehabilitation
Conditions
Interventions
Intervention group:12-week standard pulmonary rehabilitation
contron Group:none
Sponsors
The University of Hong Kong-Shenzhen Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Before any assessment, the patient or his legal representative must sign an informed consent; 2. Patients with stable COPD diagnosis; 3. Patients diagnosed with OSA; 4. Aged 18-75 years, male or female.
Exclusion criteria
Exclusion criteria: 1. History of lung cancer, cystic fibrosis, bronchiectasis or alpha-1 antitrypsin deficiency or any other significant lung disease; 2. Diagnosed as bronchial asthma, restrictive lung disease; 3. Patients who currently have or have had uncontrolled heart failure, clinically significant coronary artery disease, recent myocardial infarction, or severe hypertension that is considered uncontrolled arrhythmia; 4. Suffering from clinically or functionally uncontrollable respiratory, hematological, immunological, renal, neurological, hepatic, endocrine or other diseases or any other possible conditions (such as major surgery), which, in the judgment of the investigator, may cause The patient is at undue risk or affects the study results or interpretation of the results; 5. Patients with chronic obstructive pulmonary disease who have undergone interventional therapy, such as tracheal valve volume reduction surgery; 6. Patients with mental illnesses such as depression and anxiety disorders that affect the judgment results; 7. Conditions that prevent patients from participating in exercise in patients who cannot tolerate pulmonary rehabilitation therapy (such as severe arthritis, musculoskeletal diseases, neurological impairment, cognitive or psychosocial disorders); 8. Patients who are still smoking; 9. Patients who cannot comply with study procedures.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 6-minute walk test; | — |
Countries
China
Contacts
Public ContactWang Hongxia
The University of Hong Kong-Shenzhen Hospital
Outcome results
None listed