Effects of Whole Body Vibration (WBV) on Musculoskeletal System of Aged Women
- Conditions
- Osteopenia
- Interventions
- Device: sedentaryDevice: Vibration
- Registration Number
- NCT01982214
- Brief Summary
A controlled, non-randomized trial will be carried out in 240 postmenopausal women, aged 55-75 years, over a 18-month period. The group 1 received a physical intervention, consisting of whole body vibration (WBV) over 12 months followed by training arrest during 6 months. The group 2 served as sedentary control. WBV training is performed 2 or 3 times per week, with each session lasting 20 minutes. The training included light squats at 35-50 Hz and ended up by stretching and relaxation exercises at 50 Hz. Bone, muscle and postural evaluations will be performed at the beginning, 6, 12 and 18 months in each group with evaluation of bone micro-architectural trabecular and cortical compartments, at the weight bearing tibia and the non weight bearing radius.
The primary outcome of the project is the pre, mid, and post evaluations of bone. Bone exploration included dual x-ray absorptiometry (DXA) and high resolution peripheral quantitative computed tomography (HR-pQCT). Bone Mass Density (BMD) will be evaluated by DXA at lumbar, femoral levels and humeral, macro and micro-architectures of the cortical and trabecular compartments will be evaluated in distal radius and tibia by HR-pQCT and bone markers will be analyzed longitudinally. The secondary aim is to assess muscle performance and proprioception. Finally will be assessed markers of cartilage degradation and synthesis, no study has been published on this tissue.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- Female
- Target Recruitment
- 225
- Be sedentary (less than 2 hours physical activity of low intensity per week)
- Fracture risk Densitometry Risk factors (FRAX) index between 3 and 10%
- Consent form signed
- Bone concomitant disease (such as Paget's disease, osteomalacia),
- Endocrinopathy defined on biological criteria (such as Cushing's disease, hyperparathyroidism, hyperthyroidism, hypogonadism),
- Smoking habits (more than 5 cigarettes per day), chronic alcoholism,
- Treatments received in the previous 6 months affecting bone metabolism such as anabolics, anti-osteoporotic treatment, corticosteroids.
- Having a prosthesis (femur and knee),or recently placed metal bouts or plates
- acute thrombotic problems,
- severe heart- and vascular diseases,
- recent injuries due to operation or polyclinical intervention,
- acute hernia, discopathy, spondylolysis,
- epilepsy,
- severe migraine,
- pacemaker,
- every neurodegenerative or neuromuscular disease,
- dementia
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description sedentary sedentary No intervention Vibration Vibration Subjects in this group will be submitted to the WBV for 5 to 20 minutes, 2 or 3 times a week while 12 months. The training included light squats at 35-50 Hz and ended up by stretching and relaxation exercises.
- Primary Outcome Measures
Name Time Method Trabecular bone volume at the femoral neck 12 month bone densitometric parameters will be evaluated with DXA (dual x-ray absorptiometry)
- Secondary Outcome Measures
Name Time Method Serum bone markers 12 month We will evaluated the activity of bone serum markers of bone formation (amino-terminal propeptide type I procollagen, PINP) and of bone resorption (C telopeptide of type I collagen, S-CTX).
Bone cortical compartment at radius and tibia 12 month
Trial Locations
- Locations (1)
CHU de Saint-Etienne
🇫🇷Saint-etienne, France