Efficiency of a Whole Body Vibration Training Program in Adult Renal Transplanted Patients

Universidade Federal de Pernambuco

Status: Unknown

Conditions: Kidney Transplantation; Exercise

Treatments: Other: Platform sham; Other: Platform

Study type: Interventional

Funder types: Other

Identifiers

NCT03120377

LRocha

Details and patient eligibility

About

Evaluate the effectiveness of a Whole body vibration training program on quadriceps muscle strength, functional capacity and respiratory muscle strength in adult renal transplant recipients

Full description

The study will be a randomized controlled clinical trial involving adult renal transplant recipients, who will be recruited through eligibility criteria at Nephrology outpatient clinics of the Kidney Transplantation Centers of the Hospital das Clínicas of the Federal University of Pernambuco (HC-UFPE). Individuals will be randomized and assigned to one of the following groups: Platform Group, which will perform 12-week whole body vibration training or Platform SHAM Group that will receive treatment without the therapeutic effect of the platform. Afterwards, the patients will be submitted to an evaluation, a form with sociodemographic data, the clinical history of the disease and the laboratory tests will be completed, after which the pulmonary function, respiratory muscle strength, quadriceps muscle strength and thickness, postural balance , Functional capacity, quality of life, risk of falls and level of physical activity.

Enrollment: 20 estimated patients

Sex: All

Ages: 18 to 59 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• patients with more than 1 year of kidney transplant surgery
• stable graft function (creatinine <1.8 mg / dL)
• hemoglobin> 8g / dL
• age range 18 And 59
• both sexes

Exclusion criteria

• PAS> 160mmHg and PAD> 100mmHg
• Patients with neurological, diagnosed or pulmonary heart disease
• Involved in some physiotherapeutic program
• With hospitalization history for 3 months
• Pregnant
• Current or previous smokers
• That use pacemaker, screws and / or pins in the body
• Presence of acute migraines, labyrinthitis
• History of thrombosis
• Body weight greater than 120Kg
• Cognitive, visual and / or auditory deficits
• Osteomioarticular diseases that would impair evaluation procedures and / or training

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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20 participants in 2 patient groups

Platform group

Active Comparator group

Description:

Group submitted to the whole body vibration training program

Treatment:

Other: Platform

Platform sham group

Sham Comparator group

Description:

Group that will receive the whole body vibration simulation treatment without the therapeutic effect of the platform, but with vibrating platform connected with the display on and a sound device coupled with vibration-generated noise recording, but without therapeutic purposes.

Treatment:

Other: Platform sham