Sarcopenia
Conditions
Interventions
Treatment groups will be randomized at random and will consist of 66 individuals divided into sarcopenic and not sarcopenic to participate in a program of physical training with resistance training wi
Phase 2 (3rd to 6th week: 3 sets of 12 to 15 RM, 90-second rest interval between sets)
Phase 3 (7th to 12th week: 3 sets of 8 to 12 RM, 90-second rest interval between sets). The training will last for 3 months.
conventional resistance training (bodybuilding): 22 subjects (11 and 11 sar
Phase 3 (7th to 12th week: 3 sets of 8 to 12 RM, 90-second rest interval between sets). The training will last for 3 months.
Control Group: Sample Number: 22 subjects (11 and 11 sarcopenic not sarcope
Other
I02.233.543
Sponsors
Faculdade de Ciências e Tecnologia, Universidade Estadual Paulista
Faculdade de Ciências e Tecnologia, Universidade Estadual Paulista
Eligibility
Age
60 Years to 99 Years
Inclusion criteria
Inclusion criteria: Individuals must be aged 60 or over; both genders; be clinically stable.
Exclusion criteria
Exclusion criteria: Inability to get around; being bedridden; musculoskeletal dysfunction.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Increased muscle strength of the patients in both resistance training and maintenance programs in the control group; Verified by digital dynamometer; from the realization of a range of at least 5% in the pre and post intervention measurements. | — |
Secondary
| Measure | Time frame |
|---|---|
| Improvement in functional capacity more evident in patients 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 the pre and post intervention measurements.;Increase of anti-inflammatory cytokines in patients in both resistance training groups and maintenance in the control group; verified by method of blood ELISA analysis; from the realization of a range of at least 5% in the pre and post intervention measurements.;Improve of insulin resistance more evident in patients elastic resistance group compared to conventional group and maintenance of the control group; verified by colorimetric method of blood analysis; from the realization of a range of at least 5% in the pre and post intervention measurements. | — |
Countries
Brazil
Contacts
Public ContactLuís Gobbo
Faculdade de Ciências e Tecnologia, Universidade Estadual Paulista
Outcome results
None listed