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Comparison of PR Efficiency in Home-based With Hospital-based PR in Bronchiectasis

M

Medipol Health Group

Status

Enrolling

Conditions

Lung Diseases, Interstitial
Bronchiectasis
Lung Diseases
Pulmonary Rehabilitation

Treatments

Other: Home-based pulmonary rehabilitation
Other: Hospital-based pulmonary rehabilitation

Study type

Interventional

Funder types

Other

Identifiers

NCT03561818
PR_bronchiectasis

Details and patient eligibility

About

The investigators aimed to compare the home-based Pulmonary Rehabilitation with the hospital-based pulmonary rehabilitation in terms of pulmonary rehabilitation efficiency in patient with bronchiectasis.

Full description

While the benefits of pulmonary rehabilitation (PR) in cases of chronic obstructive pulmonary disease (COPD) have been well-documented, there have been only a limited number of studies investigating the efficacy of PR in patients with bronchiectasis. Some of these studies have reported positive effects of PR also in bronchiectasis patients, but have underlined the need for additional studies including larger patient groups to define PR indications, and to ensure that exercise protocols are specific for this patient group. There are many PR organizational types, such as hospital-based, telephone-mentoring with home-based or tele monitorization programs. Hospital-based supervised programs are time-consuming and costly practices. For this reason, there is a need for further studies on the effectiveness and benefits of unsupervised programs. In this study, we will compare unsupervised home-based PR and supervised hospital-based PR in terms of pulmonary rehabilitation effectiveness.

The pulmonary function tests, dyspnea perception, quality of life and exercise capacity assessments will performed before and after pulmonary rehabilitation.

Enrollment

50 estimated patients

Sex

All

Ages

18 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Between the ages of 18-70
  • Patients signing informed consent form
  • Bronchiectasis patients in the stable phase who were diagnosed with High-resolution computed tomography (HRCT).

Exclusion criteria

  • Decompensated heart failure, uncontrolled hypertension (Systolic Blood Pressure> 200, Diastolic Blood Pressure> 110),
  • Additional diseases that may prevent exercise,
  • To be regularly exercising regularly

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

50 participants in 2 patient groups

Hospital-based group
Experimental group
Description:
2 months hospital-based pulmonary rehabilitation program
Treatment:
Other: Hospital-based pulmonary rehabilitation
Home-based group
Experimental group
Description:
2 months home-based pulmonary rehabilitation program
Treatment:
Other: Home-based pulmonary rehabilitation

Trial contacts and locations

1

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Central trial contact

Esra Pehlivan, PhD

Data sourced from clinicaltrials.gov

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