Can special breathing exercises help COPD patients breathe easier? new study aims to find out.
NCT ID NCT07415746
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study will test whether a pulmonary rehabilitation program that includes inspiratory muscle training (using a device called Powerbreathe) can improve diaphragm function in people with COPD. Researchers will use ultrasound to measure diaphragm movement and thickness before and after the program. The goal is to see if these exercises help reduce symptoms like shortness of breath and fatigue. The study plans to enroll 46 adults aged 40 and older with stable COPD.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Pulmonary rehabilitation with inspiratory muscle training (Powerbreathe device) and resistance/aerobic exercise
- What this could lead to
- If successful, this could show that combining inspiratory muscle training with standard rehab improves diaphragm function and reduces symptoms like shortness of breath in COPD patients.
- What could go wrong
- This is a small, early-stage study (46 participants) that is not yet recruiting. It focuses on measuring changes, not on proving a new treatment works, so results may not lead to a new therapy.
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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About 46 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Mar 2026
An estimate. Start dates often move.
- Expected to finish
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Oct 2026
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: * Age 40 years or older. * Both sexes are eligible (men and women). * Clinically diagnosed COPD, clinically stable, classified in Stages I, II, III or IV of GOLD (Global Initiative for Chronic Obstructive Lung Disease). * Ability to understand and provide the signed Informed Consent Form to participate in the study. Exclusion Criteria: * Physical limitations and/or cognitive impairment that prevent the execution of the study protocol. * Currently engaged in physical therapy treatment and/or physical activity that may interfere with the study results. * Presence of severe, uncontrolled, or disabling comorbidities.
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Teaching and Assistance Unit in Physiotherapy and Occupational Therapy
Belém, Pará, 66093605, Brazil
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