Effect of Resistance Training Associated With Whole-Body Vibration in Diabetes

Universidade Federal de Pernambuco

Status: Unknown

Conditions: Diabetes Mellitus, Type 2

Treatments: Other: Resistance training associated with vibration; Other: Resistance training associated with vibration sham

Study type: Interventional

Funder types: Other

Identifiers

NCT03443986

Resistance, Vibration and DM

Details and patient eligibility

About

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.

Enrollment: 60 estimated patients

Sex: All

Ages: 60 to 80 years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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60 participants in 3 patient groups

Resistance training associated with vibration

Experimental group

Description:

The workout will be held three times a week and will last a total of 12 weeks (3 months) for 45 minutes.

Treatment:

Other: Resistance training associated with vibration

Resistance training associated with sham

Sham Comparator group

Description:

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 "sham" and 5 minutes of slowdown. The vibration sham; will be held with the disconnected platform. A device will be connected producing a noise similar to the sound of the connected platform for a time equivalent to the treatment protocol, since it will not be possible to distinguishing noticeably stimulate vibrator. Participants that will undergo false vibration will not have contact with those who carry out the real treatment.

Treatment:

Other: Resistance training associated with vibration sham

Control group

No Intervention group

Description:

Will not be submitted to any physical intervention. It continues in your daily life with only monitoring via phone callings. Guidelines about foot care.