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Recruiting NCT03561818

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

No phase Interventional Bronchiectasis Pulmonary Rehabilitation Lung Diseases Lung Diseases, Interstitial

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Hospital-based pulmonary rehabilitation, Home-based pulmonary rehabilitation.
Who it may be relevant to
Registry conditions: Bronchiectasis, Pulmonary Rehabilitation, Lung Diseases, Lung Diseases, Interstitial. Basic parameters: 18 years — 75 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Comparison of Pulmonary Rehabilitation Efficiency in Home-based With Hospital-based Pulmonary Rehabilitation in Bronchiectasis

Overview

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.

Detailed 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.

Interventions

  • Other Hospital-based pulmonary rehabilitation
    The patients who undergo two days pulmonary rehabilitation under supervision in our clinic and three days a week at home during two months will taken as hospital group. The exercises include breathing exercises, treadmill (15sc), cycle training (15sc), arm ergometer training (15sc), peripheral muscle training and stretching exercises with free weights.
  • Other Home-based pulmonary rehabilitation
    The patients who follow a home-based pulmonary rehabilitation program for two months comprising breathing exercises, training in chest hygiene techniques, peripheral muscle strengthening training and self-walking for 5 days in a week for two months. An exercise follow-up form will give to the patients to record their daily exercises. A similar form will fill by physiotherapist once a week during phone call.

Primary outcome measures

  • Changes from baseline the 6-minute walking distance at two months. [Time frame: Two months]
  • Changes from baseline the modified Medical Research Council (mMRC) scale at two months. [Time frame: Two months]
Secondary outcome measures (3)
  • Changes from baseline the forced expiratory volume in one second at two months. [Time frame: Two months]
  • Changes from baseline the peripheral muscle strength at two months. [Time frame: Two months]
  • Changes from baseline the Quality of Life at two months. [Time frame: Two months]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Non-randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Supportive care

Study locations

Turkey (Türkiye) · 1 center
  • Yedikule Chest Disease Hospital — Istanbul

Identifiers

NCT: NCT03561818 · PR_bronchiectasis

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗