Breathing therapy tested for heart failure – trial stopped early
NCT ID NCT05223751
First seen Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a special breathing exercise program could help people with systolic heart failure walk farther and feel better. The trial planned to enroll 65 adults with moderate heart failure, but it was terminated early. Participants would have been assigned to either standard care or standard care plus daily breathing exercises using a smartphone app and coaching.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- breathing exercises (Meo Health breathing therapy)
- What this could lead to
- If it worked, this could offer a simple, drug-free way to help people with heart failure feel better and walk farther.
- What could go wrong
- The trial was terminated early, so we have limited data. It was also a small study, and results may not apply to everyone with heart failure.
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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65 people
The number who actually took part.
- Started
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Feb 2022
- Finished
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Sep 2025
- 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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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. 18 years or older 2. Signed informed consent 3. NYHA class II-III heart failure 4. EF ≤ 45% (echo within 1 year of enrollment) 5. At least 30 days of stable medical regimen (no new neurohormonal blockade or Sodium-glucose co-transporter 2 inhibitors (SGLT2i). Dose adjustments allowed) 6. Likely to be compliant with breath training as assessed by the provider 7. Availability of a "smart" phone and internet access 8. Established care at Lancaster General Health Penn Medicine Exclusion Criteria: 1. Cardiac resynchronization therapy (CRT) within 6 months 2. Severe Chronic obstructive pulmonary disease (COPD) 3. History of diaphragm paralysis 4. Unable or unwilling to complete respiratory training protocol 5. Decompensated or American College of Cardiology (ACC) Stage D Heart Failure (HF) 6. Prior or planned chest/abdominal or nasal/facial surgery within 6 months 7. Neuromuscular disease which impairs respiration 8. Diagnosed cognitive impairment (unable to participate in training) 9. Untreated obstructive severe sleep apnea (AHI \> 30) 10. Severe valvular heart disease 11. Uncontrolled atrial fibrillation (Ave Heart Rate (HR) \> 100 bpm) 12. Orthopedic or other limitations which impair the 6-minute walk test
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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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Lancaster General Hospital
Lancaster, Pennsylvania, 17604, United States
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