Diabetes Mellitus, Type 2
Conditions
Keywords
Diabetes Mellitus, Blood Flow Velocity, Skin Temperature, Postural Balance, Combined Modality Therapy, Vibration, Resistance Training
Brief summary
Introduction: Diabetes Mellitus (DM) is an important health condition of the population and its prevalence continues to grow due to population aging, economic development and urbanization. The exercise is an important factor of prevention and control, thereby decreasing the risk of metabolic diseases, cardiovascular diseases and improving the functionality of the patient with diabetes. Objective: Evaluate the response of resistance training associated with whole-body vibration on peripheral circulation and functional performance of elderly with type 2 diabetes. Methods: This is a clinical trial study, controlled, randomized and blinded, which will follow the guidelines established by the Consolidated Standards of Reporting Trials (CONSORT). Patients will be recruited in the light of the eligibility criteria and randomly divided into 3 groups: resistance training associated with whole body vibration (G1), resistance training associated with vibration sham (G2) and control group-guidelines about foot care (GC), establishing 36 treatment sessions, three times a week for the G1 and G2.
Interventions
OTHERResistance training associated with vibration
The workout will be held three times a week and will last a total of 12 weeks (3 months) for 45 minutes, where there will be 5 minutes of heating, 19 minutes of exercise with load, 16 minutes of vibration and 5 minutes of slowdown.
OTHERResistance training associated with vibration sham
he workout will be held three times a week and will last a total of 12 weeks (3 months) for 45 minutes, where there will be 5 minutes of heating, 19 minutes of exercise with load, 16 minutes of vibration sham and 5 minutes of slowdown.
Sponsors
Universidade Federal de Pernambuco
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)
Masking description
Triple: a researcher shall be exclusively responsible for the evaluations and reevaluations not having knowledge of what intervention group the patient will enter. The patient will be allocated among three groups. After the final evaluations, all data will be analyzed by another researcher directed solely to that purpose. Therefore, there will be a triple blinding (researcher, patient and statistician).
Intervention model description
Three groups: resistance training associated with whole body vibration (G1), resistance training associated with vibration sham; (G2) and control group-guidelines about foot care (GC)
Eligibility
Sex/Gender
ALL
Age
60 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
* Present overweight or obese class I, with BMI between 25.00 and 34.99 kg/m2 (WHO, 2009) * Be functionally independent * Having cognitive ability to respond and perform the exercisesevaluated by Mini-Mental State examination (MMSE), prepared by Folstein et al. (1975) and translation/modification proposed by Lawrence and van Heerden (2006), using as a bridge to cut to illiterate individuals = 19 points (BRAZIL, 2006) * Inactive (0 to 5 points) or less active (6 to 11 points) according to the Questionnaire of Habitual Physical Activity (QAFH) * Patients without severe foot deformities requiring therapeutic shoes * Do not have orthopedic deficiencies * No indications of deep vein thrombosis * Do not use locomotion auxiliary equipment
Exclusion criteria
* Change in the drug program in during the research * Performing other physical activity during the training * Hypertensive Peaks during treatment
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Peripheral circulation | 12 weeks | Vascular Doppler ultrasound (UVD) |
| Functional performance | 12 weeks | Timed Up and Go Test (TUG) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Static postural alignment | 12 weeks | Optoeletrônico system SMART DX100 |
| Plantar pressure distribution | 12 weeks | Baropodometry |
Countries
Brazil
Outcome results
None listed