Efficiency of a Whole Body Vibration Training Program in Adult Renal Transplanted Patients
- Conditions
- Kidney TransplantationExercise
- Interventions
- Other: PlatformOther: Platform sham
- Registration Number
- NCT03120377
- Lead Sponsor
- Universidade Federal de Pernambuco
- Brief Summary
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
- Detailed 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.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 20
- 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
- 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
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Platform group Platform Group submitted to the whole body vibration training program Platform sham group Platform sham 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.
- Primary Outcome Measures
Name Time Method Quadriceps muscle strength 20 minutes Will be performed the examination of the Maximum Voluntary Isometric Contraction
Functional capacity 10 minutes The 6-minute walk test will be used
Respiratory muscle strength 20 minutes Will be performed through the manocacuometry with the evaluation of the maximum respiratory pressures
- Secondary Outcome Measures
Name Time Method Pulmonary function 15 minutes Slow and forced spirometry will be used
Thickness of the quadriceps 10 minutes This measure will be obtained through the portable Ultrasound
Postural balance 20 minutes The static and dynamic postural balance will be evaluated through the Biodex Balance System
Level of physical activity 5 minutes It will be evaluated by the International Physical Activity Questionnaire
Quality of life 10 minutes Will be applied the Medical Outcomes Study Quality of Life Questionnaire - Short-Form Health Survey
Risk of fall 5 minutes The International Fall Efficiency Scale (FES-I) will be used
Trial Locations
- Locations (1)
Laboratório Cardiopulmonar
🇧🇷Recife, Pernambuco, Brazil