Efficacy of 8-week Supervision in Home Based Pulmonary Rehabilitation

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

Total Enrollment

41 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-09-01

Study Completion Date

2020-09-06

Brief Summary

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In korea, it is not easy to practice standard pulmonary rehabilitation (PR). in this study, we'll educate PR to patients and make reservation for re-visiting outpatients clinics with PR diary. we want to confirm whether patients, who perform home based PR during more than 30 minutes in 3 days per week, present improved dyspnea score or quality of life compared with non-compliance group.

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Detailed Description

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Conditions

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Chronic Obstructive Pulmonary Disease

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Interventions

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Pulmonary rehabilitation

In this study, we'll educate pulmonary rehabilitation to patients and make reservation for re-visiting outpatients clinics with PR diary after 8 weeks.

we want to confirm whether patients, who perform home based PR during more than 30 minutes in 3 days per week, present improved dyspnea score or quality of life compared with non-compliance group.

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* forced expiratory volume-one second / forced vital capacity \< 0.7 in post-bronchodilator pulmonary function test
* adults 40 years or older
* no history of acute exacerbation within 4 weeks
* no history of education for pulmonary rehabilitation within 6 months
* no change of medication for chronic obstructive pulmonary disease within 4 weeks
* dyspnea more than Modified Medical Research Council grade 0

Exclusion Criteria

* adults under 40 years old
* no consent
* history of acute exacerbation within 4 weeks
* history of education for pulmonary rehabilitation within 6 months
* change of medication for chronic obstructive pulmonary disease within 4 weeks
* dyspnea only Modified Medical Research Council grade 0
* comorbidity, including cardiovascular disease, orthopedic disease, neurologic disease, optic disease, uncontrolled hypertension
* enrolled other clinical trial
* on long term oxygen therapy

Minimum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No