Diabetes mellitus
Conditions
Interventions
This is an uncontrolled clinical study, randomized with comparator groups, with at least 50 participants in each group, totaling a minimum of 100 participants. Which will have groups of adults and sen
Sponsors
Universidade Federal de Santa Catarina
Universidade Federal de Santa Catarina
Eligibility
Age
30 Years to 80 Years
Inclusion criteria
Inclusion criteria: Be a participant in the Vertical Position Water Activities program; have medical authorization to practice physical exercise
Exclusion criteria
Exclusion criteria: Do not be disponible time for participate; have osteomioarticular limitations that may impair the execution of the exercises
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find an improvement in health-related physical fitness, assessed by the Rikli and Jones test battery, with an improvement of at least 10% in functional capacity. Data collected before and after the intervention. | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to find an improvement in random blood glucose, assessed by the capillary blood glucose test, with a reduction and/or maintenance of blood glucose levels. Data collected before and after the intervention, in addition to collections performed before, immediately and 30 minutes after the first and last session of each training mesocycle.;It is expected to find an improvement in the measurement of blood pressure, evaluated by the outpatient examination with automatic equipment, with a reduction and/or maintenance of blood pressure levels. Data collected before and after the intervention, in addition to collections performed before, immediately and 30 minutes after the first and last session of each training mesocycle.;It is expected to find an improvement in the perception of quality of life, assessed by a self-administered instrument, with a reduction of at least 1 point. Data collected before and after the intervention.;It is expected to find an improvement in depressive symptoms, assessed by a self-administered instrument, with an improvement of at least 1 point. Data collected before and after the intervention.;It is expected to find an improvement in sleep quality, assessed by a self-administered instrument, with an improvement of at least 1 point. Data collected before and after the intervention.;It is expected to find an improvement in signs and symptoms in women, assessed by a self-administered instrument. Data collected before and after the intervention.;It is expected to find an improvement in the biochemical profile (total cholesterol, LDL, HDL and triglycerides, fasting glucose, creatinine, urea, uric acid, glycated hemoglobin, C-reactive protein, interleukin-6, interleukin-10), evaluated by blood collection . Data collected before and after the intervention. | — |
Countries
Brazil
Contacts
Public ContactRodrigo Delevatti
Universidade Federal de Santa Catarina
Outcome results
None listed