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Not yet recruitingNCT07539571Updated Apr 20, 2026

Telerehabilitation in Patients With Bronchiectasis

An interventional study of telerehabilitation in Bronchiectasis and Telerehabilitation, sponsored by Hospitales Universitarios Virgen del Rocío. Not yet recruiting at 1 site in Spain. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-04-20.

Sponsored by Hospitales Universitarios Virgen del Rocío · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

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 clinical guidelines regarding the use of TR in patients with bronchiectasis.

02

Conditions studied

  • Bronchiectasis
  • Telerehabilitation

Keywords

  • Bronchiectasis
  • Telerehabilitation
  • Quality of life
  • Inflammation
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Bronchiectasis diagnosed by high resolution computed tomography (HRCT) of the chest.
  • Clinically stable patients (without hospitalizations, infection or changes in pharmacological treatment in the last month of the study beginning).
  • Both gender
  • Non smokers.
  • Internet connection available.

Exclusion criteria

Exclusion Criteria:

  • Inability to give informed consent to participate
  • Less of 18 years
  • With other lung related diseases (asthma, COPD and cystic fibrosis)
  • Decompensated cardiovascular and metabolic diseases, neuromuscular or musculoskeletal that impede the realization of the protocol.
  • Mental disorders that prevent the adequate participation in the tele-rehabilitation program.
  • Simultaneous participation in another clinical trial.
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Care provider, Outcomes assessor)
Enrollment
80 participants (estimated)

Study arms

  • No intervention
    Usual care group

    Standard care for exacerbation and follow-up without rehabilitation.

  • Experimental
    Exercise group

    Telerehabilitation: 12 weeks of supervised exercise interventions.

    Other: telerehabilitation

Interventions

  • Othertelerehabilitation

    3 days per week: supervised resistance training that includes upper and lower limb and core exercises, initially using with low weights, performed in 2 sets with 10 repetitions, with progressive weekly increases depending on symptoms. 4 days per week: endurance training. Patients will walk on days when they do not perform strength training, for at least 30 minutes, with the duration gradually increased each month depending on their symptoms.

    Also known as: physical activity

05

What researchers measure

Primary outcomes

  1. 6-minute walk distance

    Patients walk through a 30-meter corridor faster than they can for 6 minutes

    Time frame: Baseline, week 6, after 12 weeks of telerehabilitation program, and at 3 and 6 months after completing the telerehabilitation program.

Secondary outcomes

  1. The quality of life

    ST Georges respiratory questionnaire COPD assessment test. Scores range from 0 to 100, where 0 represents the best possible health (no limitations) and 100 the worst health status.

    Time frame: Baseline, after 12 weeks of telerehabilitation program and at 3 and 6 months after completing the telerehabilitation program.

  2. Pulmonary function tests

    pulmonary function tests (FEV1, FVC)

    Time frame: Baseline and after 12 weeks of telerehabilitation program.

  3. Respiratory Muscle Strength

    Maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP).

    Time frame: Baseline and after 12 weeks of telerehabilitation program.

  4. Exahled Nitric Oxide Fraction (FeNO)

    Exahled Nitric Oxide Fraction (FeNO)

    Time frame: Baseline and after 12 weeks of telerehabilitation program.

  5. Sputum microbiology

    The presence of Pseudomonas Aeruginosa through microbiological analysis of sputum

    Time frame: Baseline, after 12 weeks of telerehabilitation program, and at 3 and 6 months after completing the telerehabilitation program.

  6. Biological markers of Biological markers of inflammation

    PCR, neutrophil/lymphocyte ratio, IL-1β, IL-6, TNF-α levels.

    Time frame: Baseline and after 12 weeks of telerehabilitation program.

  7. Dyspnoea

    Modified Medical Research Council (mMRC) dyspnoea scale. Minimum value (Grade 0): Absence of dyspnea. Maximum value (Grade 4): Severe dyspnea.

    Time frame: Baseline, week 6, after 12 weeks of telerehabilitation program, and at 3 and 6 months after completing the telerehabilitation program.

  8. Bronchiectasis severity

    The E-FACED questionnaire. Scores range from 0 to 9, where a score of 0-3 indicates mild severity, 4-6 indicates moderate severity, and ≥ 7 indicates severe disease.

    Time frame: Baseline and after 12 weeks of telerehabilitation program.

  9. Change from baseline in respiratory symptoms and adverse events.

    Change from baseline in respiratory symptoms and adverse events.

    Time frame: Baseline, week 6, after 12 weeks of telerehabilitation program, and at 3 and 6 months after completing the telerehabilitation program.

  10. Blood pressure

    Measurement of blood pressure using a sphygmomanometer. Blood Pressure Ranges in Adults: Normal: Less than 120/80 mmHg. Elevated: 120-129 / \< 80 mmHg. Hypertension Grade 1: 130-139 / 80-89 mmHg. Hypertension Grade 2: ≥ 140 / ≥ 90 mmHg.

    Time frame: Baseline, week 6, after 12 weeks of telerehabilitation program, and at 3 and 6 months after completing the telerehabilitation program.

  11. Heart rate

    The heart rate value recorded by the sphygmomanometer will be documented.

    Time frame: Baseline, week 6, after 12 weeks of telerehabilitation program, and at 3 and 6 months after completing the telerehabilitation program.

  12. Oxygen saturation (SpO2)

    Oxygen saturation is measured using a pulse oximeter. Values between 95% and 100% are considered normal. Values below 90% are considered hypoxemia. Normal values range between 95% and 100%.

    Time frame: Baseline, week 6, after 12 weeks of telerehabilitation program, and at 3 and 6 months after completing the telerehabilitation program.

  13. Exacerbation

    Exacerbation rate

    Time frame: Baseline, week 6, after 12 weeks of telerehabilitation program, and at 3 and 6 months after completing the telerehabilitation program.

  14. Telerehabilitation adherence

    Number of sessions completed by participants who take part in the rehabilitation program and training parameters registration

    Time frame: Baseline, week 6, after 12 weeks of telerehabilitation program, and at 3 and 6 months after completing the telerehabilitation program.

06

Study locations

1 site
  • Hospital Universitario Virgen del Rocío
    Seville, Sevilla 41013, Spain
07

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT07539571
Lead sponsor
Hospitales Universitarios Virgen del Rocío
Responsible party
Ana Ortega Moral (PhD Student, Hospitales Universitarios Virgen del Rocío) — Principal investigator
First posted
Apr 20, 2026
Start date
Sep 2026 (estimated)
Primary completion
Dec 2031 (estimated)
Completion
Dec 2032 (estimated)
Last update
Apr 20, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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