e-PUREDigital Pulmonary Rehabilitation for COPD Patients
Exercise
Behavior+7
+ Chronic Disease
+ Lung Diseases
Treatment Study
Summary
Study start date: March 31, 2025
Actual date on which the first participant was enrolled.This study is exploring a new digital rehabilitation program designed for people with Chronic Obstructive Pulmonary Disease (COPD) in Southwest Finland. COPD is a common condition that mostly affects older adults and can significantly reduce life quality and life expectancy. Pulmonary rehabilitation is known to improve symptoms and quality of life for these patients, but traditional programs are often hard to access. The COVID-19 pandemic made it even harder, leading to increased interest in virtual programs. This study aims to see if a digital approach is feasible and effective, potentially offering a more accessible option for COPD patients. Participants in the study will follow a 12-week personalized rehabilitation plan that includes exercises, nutritional guidance, and support to stop smoking. The plan is monitored through online questionnaires and physical tests like the 6-minute walk test. The main goal is to see if participants can walk further after the program compared to before. Other measures include patient satisfaction and changes in respiratory health as assessed by the St. George Respiratory Questionnaire. The study will also see how the program affects healthcare usage, such as hospital visits, and will help determine if a larger study should be conducted in the future.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.50 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 18 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.Conditions
Pathology
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
Study Objectives
Primary 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
Turku University Hospital
Turku, Finland