Respiratory rehabilitation in lung disease

Not Applicable

Conditions: Chronic Obstructive Pulmonary Disease (Chronic Bronchitis,Amphysema).
simple and mucopurulent chronic bronchitis,Emphysema
J41, J43

Registration Number: IRCT201105096422N1

Lead Sponsor: Mashhad University of Medical Sciences, Research Section

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Complete

Sex: All

Target Recruitment: 30

Inclusion Criteria

Obtaining informed consent, The chronic obstructive pulmonary disease diagnosed and confirmed by lung specialist and through paraclinical tests; fev1<80% predicted and fev1/fvc<70% (stageII, stable patients); clear Lungs, age 40-65; basic spirometry other than Asthma; No smoking at least for 3 months
Exclusion criteria: Refuse to participate in research; not taking part in training for 4 weeks prior to the study; fever or respiratory infection; Respiratory or cardiac failure

Exclusion Criteria

Not provided

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Maximal Voluntary Ventilation. Timepoint: before intervention, end of week 2, end of week 4. Method of measurement: L/m, by Hi 801 spirometer.;PImax. Timepoint: before intervention, end of week 2, end of week 4. Method of measurement: Cm/H20, mouth pressure meter.;Forced Vital Capasity. Timepoint: before intervention, end of week 2,end of week 4. Method of measurement: L, by Hi 801 spirometer.;Peek Expiratory Flow Rate. Timepoint: before intervention, end of week 2, end of week 4. Method of measurement: L/s, by Hi 801 spirometer.;Forced Expiratory Volume in One Second. Timepoint: before intervention, end of week 2, end of week 4. Method of measurement: L, by Hi 801 spirometer.;Tidal Volume. Timepoint: before intervention, end of week 2, end of week 4. Method of measurement: L, by Hi 801 spirometer.;Respiratory Rate. Timepoint: before intervention, end of week 2, end of week 4. Method of measurement: Count chest rising and coming down for one full minute, by watch OMax.

Secondary Outcome Measures

Name	Time	Method
Dyspnea. Timepoint: befor intervention, end of week 2, end of week4. Method of measurement: Numerical Rating Scale (0-10).;Respiratory pattern. Timepoint: before intervention, end of week 2. end of week 4. Method of measurement: with measuring depth of respiration (according to tidal volume, L) and respiratory rate by watch, Breath/minute.