RecruitingNot ApplicableNCT07090200

Rehabilitation Intervention for COPD Combined With Cardiovascular and Cerebrovascular Diseases


Sponsor

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

Enrollment

50,000 participants

Start Date

Sep 1, 2025

Study Type

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

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This trial is studying a rehabilitation program for people living with both a chronic lung disease (COPD) and heart or brain blood vessel disease, to see if it helps improve their health and daily functioning. You may be eligible if: you are 18 years or older (any gender); and you are committed to following the study program and attending all required visits. You may NOT be eligible if: you have a severe mental illness; you have a life-threatening condition requiring immediate hospitalization; you are pregnant, breastfeeding, or not using proper birth control; you refuse to complete follow-up questionnaires or provide samples; or you are currently in another drug intervention trial. Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

COMBINATION_PRODUCTPulmonary Rehabilitation Care Group

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.

OTHERThe Routine Care (Non-Pharmacological and Pharmacological Treatments ) Group

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)

Union hospital, Tongji Medical college, Huazhong University of Science and Technology

Wuhan, Hubei, China

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07090200


Related Trials