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pulmonary rehabilitation in Chronic Obstructive Pulmonary Disease

Not Applicable
Conditions
chronic obstructive pulmonary disease.
other chronic obstructive pulmonary disease
Registration Number
IRCT2015010720600N1
Lead Sponsor
Vice chancellor for research, Mashhad University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
60
Inclusion Criteria

have the desire to participate in the study? live in Mashhad; they have over 35 years of age; spoke Persian; confirmed diagnosis of COPD is confirmed by a physician and clinical results; signs of infection or exacerbations (Acute Exacerbation) based on the baseline examination by specialists not have lungs; history is not in favor of exacerbations in the past month; ability to participate in the rehabilitation program based on initial medical examination have rehabilitation medicine specialist; chronic diseases such as heart failure, coronary artery disease, other diseases known respiratory, kidney disease, arthritis, severe knee arthritis, cancer and depression is not active; history of participation in the rehabilitation program, is not; the ability to have a relationship with the researcher.
Exclusion criteria:refuse to participate in a research study and work with it; The absence of training sessions (4 sessions 3 sessions intermittent or continuous) have; exacerbation of symptoms during the rehabilitation program; Symptoms of angina, shortness of breath and severe hypoxia (Sat O2 <85%) occur during the rehabilitation program; Patients in the hospital for any reason (- Surgical) hospital.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Improvement lung function. Timepoint: Before and after the intervention. Method of measurement: Spirometric parameters, 6 minute walk test and the severity of dyspnea.
Secondary Outcome Measures
NameTimeMethod
Health-related quality of life. Timepoint: Before and after the intervention. Method of measurement: St. George's questionnaire.
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