The study protocol was approved by the Ethics Committee on Research of the Federal University of Sa ˜o Paulo
(CEP 0677/05), and the subjects provided signed informed
consent. Fifty subjects were recruited for the study, with
the following inclusion criteria: diagnosis of COPD based
on the criteria of the Brazilian Thoracic Society and Global
Initiative for Chronic Obstructive Lung Disease (GOLD),1,2
FEV
1 80% of predicted, between 40 and 75 y of age,
either gender, and signed informed consent. Exclusion
criteria included participation in a pulmonary rehabilitation program in the previous 12 months; regular practice
of any type of physical activity, such as fast walking,
swimming, or exercise at a fitness center for at least 40 min,
3 times/week, in the previous 12 months; presence of other
disease that could lead to exercise intolerance, such as
neurological, heart, or orthopedic conditions; cognitive impairment; and exacerbation in the 4 weeks before the study.
All subjects were evaluated before the intervention by spirometry, 6MWT, and a lower limb endurance test; they
also completed the St George Respiratory Questionnaire
(SGRQ) to assess quality of life. The subjects underwent
the same evaluation procedures after 24 training sessions
The study protocol was approved by the Ethics Committee on Research of the Federal University of Sa ˜o Paulo(CEP 0677/05), and the subjects provided signed informedconsent. Fifty subjects were recruited for the study, withthe following inclusion criteria: diagnosis of COPD basedon the criteria of the Brazilian Thoracic Society and GlobalInitiative for Chronic Obstructive Lung Disease (GOLD),1,2FEV1 80% of predicted, between 40 and 75 y of age,either gender, and signed informed consent. Exclusioncriteria included participation in a pulmonary rehabilitation program in the previous 12 months; regular practiceof any type of physical activity, such as fast walking,swimming, or exercise at a fitness center for at least 40 min,3 times/week, in the previous 12 months; presence of otherdisease that could lead to exercise intolerance, such asneurological, heart, or orthopedic conditions; cognitive impairment; and exacerbation in the 4 weeks before the study.All subjects were evaluated before the intervention by spirometry, 6MWT, and a lower limb endurance test; theyalso completed the St George Respiratory Questionnaire(SGRQ) to assess quality of life. The subjects underwentthe same evaluation procedures after 24 training sessions
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