Can rehab at home beat the clinic for COPD patients?
NCT ID NCT03453606
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether doing breathing and exercise training at home works as well as doing it at a rehab center for people with chronic obstructive pulmonary disease (COPD). The goal was to see if home rehab could improve exercise tolerance just as much, while also being cheaper and more convenient. The study planned to include 188 adults with moderate to severe COPD, but it was stopped early, so the full results are not available.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- respiratory rehabilitation (home-based or center-based)
- What this could lead to
- If successful, this could show that home-based rehabilitation is as effective as center-based care, offering a more convenient and cost-effective option for COPD patients.
- What could go wrong
- The trial was terminated early, so results may be incomplete. Home-based rehab may not provide the same supervision or equipment as center-based programs, potentially affecting outcomes.
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
-
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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188 people
The number who actually took part.
- Started
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Oct 2018
- Finished
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Sep 2022
- 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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18 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:According to HAS recommendations, SPLF, ERS / ATS (3) (18) (19) can be included any patient, over 18 years old, with stage II - III - IV COPD presenting disabling dyspnoea in activities of daily living, and / or in the course of acute exacerbation of COPD (EABPCO), with no other respiratory pathology diagnosed. Exclusion Criteria: According to the recommendations, HAS, SPLF, ERS / ATS will not be included any patient having : * co-morbidities including unstabilized cardiovascular disease, * significant cognitive disorders: patients with a history of pathologies neurodegenerative with loss of mental faculties (example: Alzheimer) * psychiatric disorders: patients with impaired judgment and perception * neurological or orthopedic disorders that do not allow the realization of physical activities Also, will not be included, the patient (s): * waiting for lung transplantation, * pregnant or nursing, * in an emergency situation * unable to receive enlightened information, * unable to participate in the entire study, * not covered by the social security scheme, * refusing to sign the consent,
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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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CH Victor Provot, Roubaix
Roubaix, France
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CH de Béthune
Béthune, France
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CH de Loos
Loos, France
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CH de Tourcoing
Tourcoing, France
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CH de Wattrelos
Wattrelos, France
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Centre hospitalier de béthune
Béthune, France
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Hôpital Calmette, CHU
Lille, France
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