Home video workouts may cut hospital stays for lung disease patients
NCT ID NCT05119556
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests whether a 13-week home exercise program, done via live video calls, can reduce hospital readmissions in people with COPD. 301 patients who were recently hospitalized for a COPD flare-up will either get the video rehab or standard care. The goal is to see if this approach improves breathing, quality of life, and saves money.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- video telehealth pulmonary rehabilitation (exercise sessions via videoconferencing)
- What this could lead to
- If successful, this could offer a convenient home-based program to help COPD patients avoid repeat hospital stays and improve their quality of life.
- What could go wrong
- This is a single study with 301 participants, and the intervention is behavioral, so results may vary. It may not work for everyone, and home exercise carries a small risk of injury or falls.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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301 people
The number who actually took part.
- Started
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Jun 2022
- Expected to finish
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Feb 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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40 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Age 40 or greater 2. Clinical diagnosis of COPD 3. Hospitalized for acute exacerbation of COPD. 4. Be willing to adhere to trial and follow-up procedures and give informed consent Exclusion Criteria: 1. Secondary diagnosis of congestive heart failure that is severe as documented by active symptoms, New York Heart Association (NYHA) functional classification IV or left ventricular ejection fraction \<25% on echocardiography 2. Other respiratory conditions that could confound the diagnosis such as asthma, pulmonary fibrosis, bronchiectasis, and lung cancer. Participants with pneumonic exacerbations of COPD will be included. 3. Primary diagnosis of COVID pneumonia. Individuals with incidentally detected COVID or persistently positive for COVID but deemed to be convalescent will not be excluded. 4. Active cancers on chemotherapy or radiation therapy 5. Immunosuppressed states predisposing to frequent hospitalizations including uncontrolled HIV/AIDS 6. Active or recent (within 1 month) myocardial infarction 7. Angina not well-controlled by medication 8. Unstable cardiac arrhythmias, atrial or ventricular 9. Supplemental oxygen requirement greater than 5 liters per minute at either rest or with exertion 10. Significant cognitive dysfunction, including dementia, that in opinion of investigator would impair ability to safely or effectively engage in study protocol 11. Participants with any terminal medical illnesses as diagnosed by a physician, and/or on hospice 12. Currently enrolled in and participating in pulmonary rehabilitation 13. Treatment with chronic or newly initiated home ventilatory support. Those on in-patient short-term non-invasive ventilation will not be excluded. 14. Special patient groups such as prisoners and institutionalized patients 15. Participants with musculoskeletal comorbidities or physical infirmities that preclude participation in an exercise program 16. Current participation in any other interventional clinical trial 17. Inability to understand and speak English during exercise sessions 18. Inability or unwillingness to comply with study and/or follow-up procedures outlined in the protocol
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Baylor College of Medicine
Houston, Texas, 77030, United States
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Boston VA Hospital
Boston, Massachusetts, 02130, United States
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Cincinnati VA Hospital
Cincinnati, Ohio, 45220, United States
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Cleveland Clinic
Cleveland, Ohio, 44195, United States
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HealthPartners Institute
Bloomington, Minnesota, 55440, United States
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Johns Hopkins University
Baltimore, Maryland, 21287, United States
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Minnesota VA HealthCare System
Minneapolis, Minnesota, 55455, United States
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Northern Westchester Hospital/Northwell Health
Chappaqua, New York, 10514, United States
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Northwestern Memorial Hospital
Chicago, Illinois, 60611, United States
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Temple University Hospital
Philadelphia, Pennsylvania, 19122, United States
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University of Alabama at Birmingham
Birmingham, Alabama, 35233, United States
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University of Iowa
Iowa City, Iowa, 52242, United States
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University of Maryland
College Park, Maryland, 20742, United States
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University of Pittsburgh
Pittsburgh, Pennsylvania, 15260, United States
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Wake Forest University
Winston-Salem, North Carolina, 27109, United States
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