Rehabilitation Intervention for COPD Combined With Cardiovascular and Cerebrovascular Diseases
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
50,000 participants
Sep 1, 2025
INTERVENTIONAL
Conditions
Summary
Firstly, to screen out the high-risk population of COPD combined with cardiovascular and cerebrovascular diseases, COPD with cardiovascular and make a diagnosis. Then, to evaluate the therapeutic effect of Pulmonary rehabilitation exercise and usual care for three months. And finally, to build a trinity model of rehabilitation management of COPD patients. The objective of this project is to establish and promote the application of diagnostic and treatment norms.
Eligibility
Inclusion Criteria3
- Committed to adhering to the study protocol and cooperating with the implementation of the entire research process.
- Aged 18 years or older, regardless of gender.
- Signed informed consent form.
Exclusion Criteria5
- Individuals with severe mental illness.
- Individuals assessed by medical personnel as having a disease that requires immediate hospitalization or a severe, uncontrollable condition that is life-threatening in the short term.
- Women who are pregnant, breastfeeding, or using inappropriate contraception methods.
- Individuals who refuse to cooperate with follow-up questionnaires or specimen collection.
- Patients currently participating in other interventional clinical drug trials.
Interventions
participants were randomized (1:1) to either the optimized or routine group via a computer-generated random number table. The Routine Care Group received treatment for three months and follow-up with medications prescribed according to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) 2025 Report. The Pulmonary Rehabilitation Care Group received the Pulmonary rehabilitation exercise and usual care for three months. Next, Observe the changes in the improvement of acute exacerbation frequency (times/year/person)，CAT Scoring and St. George's Respiratory Questionnaire (SGRQ), as well as lung ventilation and diffusion function of the two groups of patients one year after the intervention.
participants were randomized (1:1) to either the optimized or routine group via a computer-generated random number table. The Routine Care Group received treatment for three months and follow-up with medications prescribed according to the Global Initiative for Chronic Obstructive Lung Disease (GOLD) 2025 Report. Next, Observe the changes in the improvement of acute exacerbation frequency (times/year/person)，CAT Scoring and St. George's Respiratory Questionnaire (SGRQ), as well as lung ventilation and diffusion function one year after the intervention.
Locations(1)
View Full Details on ClinicalTrials.gov
For the most up-to-date information, visit the official listing.
NCT07090200