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Telerehabilitation in Patients With Bronchiectasis

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Summary

The NIH registered a new randomized controlled trial (NCT07539571) on ClinicalTrials.gov evaluating home-based telerehabilitation for patients with bronchiectasis. The single-center trial will be conducted at Virgen del Rocío University Hospital in Spain, randomizing participants to usual care or a 12-week supervised telerehabilitation program three times per week. Outcome measures include the 6-minute walk test, quality-of-life questionnaires, pulmonary function tests, and inflammatory biomarkers.

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What changed

The NIH has added a new clinical trial registration (NCT07539571) for a randomized controlled trial studying telerehabilitation in patients with bronchiectasis. The trial will recruit patients from Virgen del Rocío University Hospital in Spain and randomly assign them to a control group receiving usual care or an intervention group undergoing 12 weeks of supervised physical training three times per week. Assessments will be conducted at baseline and after the intervention period.

Healthcare providers and researchers interested in pulmonary rehabilitation and digital health interventions should note this trial as it may generate evidence on the effectiveness of home-based telerehabilitation for bronchiectasis patients. The trial is registered on ClinicalTrials.gov as an informational record and does not create compliance obligations.

Archived snapshot

Apr 21, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

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Telerehabilitation in Patients With Bronchiectasis

N/A NCT07539571 Kind: NA Apr 20, 2026

Abstract

Background: Home-based telerehabilitation (TR) has demonstrated benefits comparable to conventional rehabilitation in patients with chronic obstructive pulmonary disease, asthma, and pulmonary fibrosis. However, TR has not been thoroughly investigated in patients with bronchiectasis, despite evidence suggesting improvements in exercise capacity and quality of life.

Aims: To evaluate the effects of TR on functional capacity, quality of life, and inflammatory biomarkers, as well as its safety in patients with bronchiectasis.

Study design: Single-center randomized controlled trial with a parallel-group design.

Methods: Patients diagnosed with bronchiectasis will be recruited from the Surgical Medical Unit for Respiratory Diseases at Virgen del Rocío University Hospital. Participants will be randomly assigned to one of two groups: a control group receiving usual care, and a TR group undergoing supervised physical training for 12 weeks, three times per week. Outcome measures will include the 6-minute walk test, quality-of-life questionnaires, pulmonary function tests, symptom assessment, and adverse event recording, as well as sputum microbiology and analysis of inflammatory biomarkers. Assessments will be conducted at baseline and at the end of the intervention.

Expected results: A 12-week TR program is expected to significantly improve exercise capacity and quality of life in the intervention group. Additionally, this study may contribute to the development of future clin...

Conditions: Bronchiectasis, Telerehabilitation

Interventions: telerehabilitation

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Last updated

Classification

Agency
NIH
Published
April 20th, 2026
Instrument
Notice
Branch
Executive
Legal weight
Non-binding
Stage
Final
Change scope
Minor

Who this affects

Applies to
Healthcare providers Patients
Industry sector
6211 Healthcare Providers
Activity scope
Clinical trial registration Telerehabilitation study
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Clinical Operations
Topics
Pharmaceuticals Public Health

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