Rehabilitation
Conditions
Interventions
Treatment groups will be randomized at random and will consist of seventy-five patients with chronic obstructive pulmonary disease (COPD) that participate in a pulmonary rehabilitation program with re
fourth to sixth week: 3x15 RM
seventh to ninth week: 3x10 RM
tenth to twelfth week: 4x6 RM. The training will last three months
conventional resistance training (bodybuilding): twenty-five subjects will be submitted to resistance training (strength) in weight m
tenth to twelfth week: 4x6 RM. The training will last three months.
Control group: Sample Number: twenty-five individuals. For the control group there will be no type of intervention will be carried o
Other
I02.233.543
Sponsors
Faculdade de Ciências e Tecnologia - Unesp
Faculdade de Ciências e Tecnologia - Unesp
Eligibility
Age
45 Years to 70 Years
Inclusion criteria
Inclusion criteria: Patients must have a diagnosis of chronic obstructive pulmonary disease; both genders; tifennau index less than 70 percent; be aged between 45 and 70 years; being clinically stable.
Exclusion criteria
Exclusion criteria: Cardiac comorbidities and musculoskeletal disorders; exacerbation within one month of the initial evaluation.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Increased muscle strength of the patients in both resistance training and maintenance programs in the control group; checked by digital dynamometer; based on the statement of a variation of at least 5% in pre and post intervention measurements. | — |
Secondary
| Measure | Time frame |
|---|---|
| Improved functional capacity of patients most evident in elastic resistance group compared to conventional and maintenance in the control group; verified by the 6-minute walk test (6MWT); from the realization of a range of at least 5% in pre and post intervention measurements. ;Increase in anti-inflammatory cytokines in patients in both resistance training groups and maintenance in the control group; verified by blood test method ELISA ; from the realization of a range of at least 5% in pre and post intervention measurements. | — |
Countries
Brazil
Contacts
Public ContactErcy Ramos
Universidade estadual paulista- UNESP
Outcome results
None listed