Comparison of the Effectiveness of Home and Hospital-based PR in Candidate Patients With BLVR

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

66 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-05-15

Study Completion Date

2018-12-01

Brief Summary

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The recent years, the use of bronchoscopic lung volume reduction in emphysema patients instead of surgical operations has become widespread. Before this procedure, the implementation of Pulmonary Rehabilitation became a necessity. The inadequacy of the number of Pulmonary Rehabilitation Centers in our country and in our city and the increasing number of mentioned operations have increased the need for different exercise program applications. Prior to valve and coil applications in our study, changes in clinical conditions of patients will be examined if Pulmonary Rehabilitation is performed at home or in a hospital.

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Detailed Description

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The records of emphysema patients referred to the Pulmonary Rehabilitation Unit for prophylactic pulmonary rehabilitation prior to bronchoscopic lung volume reduction will be recorded prospectively. Two parallel groups will be formed from patients with hospital-based pulmonary rehabilitation (Group 1) and those with home-based pulmonary rehabilitation (Group 2). The patient will receive an 8-week Pulmonary Rehabilitation Exercise Program and will be reevaluated after 8 weeks. The differences in the parameters of initial and rehabilitation end-tracing and the differences between the groups will be examined.

Conditions

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Emphysema Bronchoscopic Lung Volume Reduction Hospital-based Pulmonary Rehabilitation Home-based Pulmonary Rehabilitation

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Two parallel groups will be formed from patients with hospital-based pulmonary rehabilitation (Group 1) and those with home-based pulmonary rehabilitation(Group 2).

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Hospital-based PR group

The patient will receive an 8-week supervised Pulmonary Rehabilitation Exercise Program at hospital

Group Type EXPERIMENTAL

Hospital-based pulmonary rehabilitation

Intervention Type OTHER

The patient will receive an 8-week Pulmonary Rehabilitation Exercise Program including breathing exercises, treadmill walking, cycle ergometer, arm ergometer training and strengthening trainning with free weights at hospital.

Home-based PR group

The patient will receive an 8-week Pulmonary Rehabilitation Exercise Program at home

Group Type EXPERIMENTAL

Home-based pulmonary rehabilitation

Intervention Type OTHER

The patient will receive an 8-week Pulmonary Rehabilitation Exercise Program including breathing exercises, free-walking, and strengthening training with free weights at home

Interventions

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Hospital-based pulmonary rehabilitation

The patient will receive an 8-week Pulmonary Rehabilitation Exercise Program including breathing exercises, treadmill walking, cycle ergometer, arm ergometer training and strengthening trainning with free weights at hospital.

Intervention Type OTHER

Home-based pulmonary rehabilitation

The patient will receive an 8-week Pulmonary Rehabilitation Exercise Program including breathing exercises, free-walking, and strengthening training with free weights at home

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patients with emphysema and bronchoscopic lung volume reduction procedures decided by chest physician
* Acceptance of participation in a 2-month Pulmonary Rehabilitation program.