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Clinical Trial Summary

The wearable vibration device aims to consistently deliver vibrations directly to the hip and spine and allowing use during many everyday activities. We propose that demonstrating higher rates of compliance and consistent delivery of optimal force, with accelerometer feedback, will provide a superior alternative to whole body vibration and is plausibly more effective at preventing bone loss in postmenopausal women than vibration platforms in the home setting.


Clinical Trial Description

The goal of this study is to demonstrate that postmenopausal women will tolerate our device, have high rates of compliance with the study protocol, receive consistently therapeutic levels of vibration and see significant effects on bone turnover based on plasma markers of bone anabolism and catabolism. The anticipated outcomes from serum draws are an improvement in two bone turnover markers after a 30 minute treatment with the WVD. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03688282
Study type Interventional
Source Theranova, L.L.C.
Contact
Status Completed
Phase N/A
Start date July 11, 2018
Completion date April 17, 2019

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