Breathing training program for improving exercise capacity in patients with non-cystic fibrosis bronchiectasis
Official title: Home-based, Digitally Delivered Breathing Training in People With Non-cystic Fibrosis Bronchiectasis: A Randomized Control Trial
Run by Mayo Clinic · NCT05860803 · Data updated 2026-11-12
This study is testing if a home breathing training program can help people with non-cystic fibrosis bronchiectasis exercise better and improve their lung function.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 21 Years to 80 Years |
| Sex | All |
| Enrollment | 50 (estimated) |
| Sponsor | Mayo Clinic Academic / other |
| Locations | 1 site (Jacksonville, Florida) |
| Status | Recruiting |
| Started | January 15, 2024 |
| Main results expected | December 1, 2026 |
| Study ends | December 1, 2026 |
| Registry record updated | January 6, 2026 |
| Trial ID | NCT05860803 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are patients with a confirmed diagnosis of non-cystic fibrosis bronchiectasis who are clinically stable and able to provide informed consent.
✕Probably not a fit
Patients with significant coexisting diseases, advanced heart failure, or recent acute exacerbations may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This research investigates the effects of a home-based breathing and respiratory muscle training program, supported by a health coach, on exercise capacity and lung function in individuals diagnosed with non-cystic fibrosis bronchiectasis. Participants will engage in a structured regimen using LungTrainers to enhance their respiratory muscles and overall clinical status. The study aims to determine if this intervention can lead to significant improvements in the ability to exercise and quality of life for these patients.
Why it matters
Potential benefit: If successful, this program could significantly enhance exercise capacity and lung function for patients with non-cystic fibrosis bronchiectasis.
How similar studies have gone: Other studies have shown promising results with similar breathing training approaches, indicating potential for success in this intervention.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Mayo Clinic patient with confirmed diagnosis of Non-Cystic Fibrosis Bronchiectasis (non-CFB): Non-CFB as confirmed by clinical history, including cough, shortness of breath, exertional dyspnea, pulmonary function tests, and high-resolution computed tomography. Patients will be considered clinically stable if there is no evidence of an exacerbation or change(s) in medical therapy in the previous three weeks. * Able and willing to provide informed consent to participate in the study. Exclusion Criteria: * Presence of significant coexisting disease, neurological conditions, and/or orthopedic complications that affect ability to undertake exercise. * Presence of advanced heart failure. * Current use of antibiotics. * Acute exacerbation(s) within 3-weeks prior to study commencement. * Participation within a pulmonary rehabilitation program within 6-months prior to study commencement.
Where it's running
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Mayo Clinic Florida
Jacksonville, Florida, United States Recruiting
Study contacts
- Principal investigator: Bryan Taylor, PhD — Mayo Clinic
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Galvokimig vs placebo for non-CF bronchiectasis in adults
This study tests whether Galvokimig can delay the first pulmonary flare compared with placebo in adults with non-CF bronchiectasis.
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Safety test of HSK31858 in people with non-cystic fibrosis bronchiectasis
This phase 3 study tests whether HSK31858 is safe for adults with non-cystic fibrosis bronchiectasis who previously participated in the related study.
-
Azithromycin added to usual care to see if it lowers bronchiectasis flare-ups
This trial tests whether taking azithromycin daily for a year reduces bronchiectasis-related flare-ups in adults with non-cystic fibrosis bronchiectasis.
-
Bronchiectasis Phenotype Identification Model for Adults
This study tests a baseline classifier to categorize adults with non-cystic fibrosis bronchiectasis into phenotype groups using data collected over time.
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BASE: Aiming to test a simple, objective way to gauge bronchiectasis severity and predict flare-ups
This study tests a new BASE framework to classify how severe non-cystic fibrosis bronchiectasis is right now and see if it can predict 12 months of worsening or flare-ups.
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Nebulized CSL787 (inhaled IgG) to reduce lung flare-ups in adults with non-cystic fibrosis bronchiectasis
This research will test whether inhaled CSL787 (a nebulized immunoglobulin medicine) can delay or reduce lung flare-ups in adults with non-cystic fibrosis bronchiectasis over 6–12 months compared with placebo.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.