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Construction and empirical study of a graded pulmonary rehabilitation program for AECOPD based on the Triangle model

Construction and empirical study of a graded pulmonary rehabilitation program for AECOPD based on the Triangle model

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300072409
Enrollment
Unknown
Registered
2023-06-13
Start date
2023-07-01
Completion date
Unknown
Last updated
2023-06-18

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

Conditions

Chronic Obstructive Pulmonary Disease

Interventions

Control group :Conventional Pulmonary Rehabilitation
Research Group :Implementation of graded pulmonary rehabilitation

Sponsors

The Second Affiliated Hospital of Zunyi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: ?Clear diagnosis of AECOPD according to the diagnostic criteria of the 2022 edition of the GOLD guidelines ?Age between 18 and 75 years old ?Conscious, with no impairment in verbal communication and able to cooperate in completing pulmonary rehabilitation exercises. ? not having received any other form of pulmonary rehabilitation instruction and exercise prior to enrollment. ? Voluntarily participate in pulmonary rehabilitation treatment and cooperate in completing the examination of related items.

Exclusion criteria

Exclusion criteria: ? serious cardiovascular disease: unstable angina, severe arrhythmia, recent myocardial infarction, congestive heart failure, severe heart failure (cardiac function graded as grade IV). ? the combination of pulmonary encephalopathy, acute attacks of bronchial asthma, active tuberculosis, pulmonary embolism, giant pulmonary blister, pneumothorax and other respiratory diseases affecting pulmonary rehabilitation therapy. ? the presence of motor neuromuscular diseases, bone and joint lesions, limb disorders, deep vein thrombosis, etc. affecting ? The need for invasive mechanical ventilation. ? Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
Pulmonary function; 6-minute walk experiment;Borg dyspnea scale;Total length of stay;Incidence of complications; Inflammatory indicators;

Secondary

MeasureTime frame
Inflammatory indicators;Chronic Obstructive Lung Self-Assessment Test;Anxiety Depression Inventory;Barthel Index;

Countries

China

Contacts

Public ContactNaNa YANG

Zunyi Medical University

265541747@qq.com+86 182 7551 3804

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 18, 2026