Home-Based Pulmonary Rehabilitation for COPD Post-Hospitalization
This study aims to evaluate how effective and helpful a home-based pulmonary rehabilitation program is for individuals with chronic obstructive pulmonary disease who have recently been hospitalized, focusing on their adherence and improvements in quality of life.
Intervention- Home-based Pulmonary Rehabilitation
Treatment Study
Summary
Study start date: November 30, 2020
Actual date on which the first participant was enrolled.This clinical trial focuses on improving the management of Chronic Obstructive Pulmonary Disease (COPD) by increasing participation in Pulmonary Rehabilitation (PR). Many people with COPD do not receive PR, even though it has proven benefits. The traditional approach of center-based rehabilitation does not meet the needs of all patients, especially after hospitalizations due to COPD-related issues like exacerbations or pneumonia. With the rise of telehealth following the COVID epidemic, this study explores a home-based, unsupervised PR program as an alternative. This method aims to be both safe and effective, potentially offering a more accessible option for patients to improve their health after leaving the hospital. Participants in the study are randomly assigned to either a home-based PR program or given a choice between home-based and traditional center-based PR after being discharged from the hospital. The study will track how many participants complete the PR program over three months, evaluating adherence as a primary measure. Additionally, the research measures changes in health-related quality of life using tools like the EuroQol (EQ-5D) and the Chronic Respiratory Questionnaire (CRQ). These tools assess various aspects of health, such as mobility, pain, and emotional well-being, providing a comprehensive picture of the participants' progress and the effectiveness of the rehabilitation approach.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.296 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Treatment Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.Over 40 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 2 locations
Mayo Clinic in Rochester
Rochester, United States