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Health Benefits of Whole-body Vibration

Pilot Investigation on the Health Benefits of Sub Acute (12 Week) Whole-body Vibration Training

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05097885
Acronym
VIBE-Rx
Enrollment
40
Registered
2021-10-28
Start date
2022-02-28
Completion date
2028-01-01
Last updated
2025-01-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Whole-body Vibration

Brief summary

The overall goals of this pilot investigation are to determine 1) the feasibility of conducting home based WBV studies, and 2) to determine if sub-acute home based WBV can improve a) exercise capacity, b) conduit- and micro- vascular function, and c) skeletal muscle function.

Detailed description

Cardiovascular disease (CVD) is the leading cause of death in the world and many comorbid conditions (i.e. diabetes, obesity) can affect overall CVD risk. There is increasing interest into the role that skeletal muscle health plays in mediating CVD risk, particularly in metabolic disease states (ie. obesity and diabetes). Whole body vibration (WBV) has emerged as an exercise mimetic that may be more tolerable than traditional modes of exercise, such as treadmill walking/running or cycling. Similar to traditional exercise modalities, WBV can elicit beneficial metabolic effects. In fact, a single bout of WBV increases circulating concentrations of IL-6, which correspond with the normalization of glucose and insulin in obese individuals. The proposed pilot investigation will provide the foundation to begin understanding the molecular and physiological mechanisms of how sub-acute WBV can improve overall CVD risk. We hypothesize that home based WBV will decrease CVD risk by improving skeletal muscle and vascular function via a decrease in systemic inflammation.

Interventions

Participants will be given a personal vibration plate to take home with them for training which will last for 12 weeks. For the first four weeks, participants will be asked to complete 10 minutes of WBV per day (1 minute on and up to 1 minute of rest), at least 3-4 days per week. At least 24 hours will be recommended in between sessions during weeks 1-4. Beginning at week 5, participants will be asked to increase WBV time to up to 14 minutes and/or reduce the duration of rest. Beginning at week 9, participants will be asked to increase WBV time to up to 20 minutes and/or reduce the duration of rest.

Sponsors

Augusta University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Men and women (\> 18 yrs old) * All races

Exclusion criteria

* \<18 years old * Clinical diagnosis of hepatic, cardiovascular, or renal disease * Diabetic complications (i.e. macrovascular, microvascular, or autonomic) * Pregnancy * Direct vasoactive medications (i.e. nitrates)

Design outcomes

Primary

MeasureTime frameDescription
Change in VO2 Peakpre-treatment baseline and following 12 weeks sub-acute whole-body vibrationchange from baseline relative (mL/kg/min) peak oxygen consumption (VO2) during maximal exercise test at 12 weeks
Change in Flow-Mediated Dilation (FMD)pre-treatment baseline and following 12 weeks sub-acute whole-body vibrationchange from baseline brachial artery flow mediated dilation at 12 weeks.
Change in Skeletal Muscle Mitochondrial Functionpre-treatment baseline and following 12 weeks sub-acute whole-body vibrationchange from baseline skeletal muscle mitochondrial function at 12 weeks. Measured using Near Infrared Spectroscopy (NIRS). Values are an index of phosphocreatine recovery expressed as a rate constant (min-1)
Change in Pulse Wave Velocity (PWV)pre-treatment baseline and following 12 weeks sub-acute whole-body vibrationChange from baseline PWV at 12 weeks. Measured by Shygmocor Xcel in m/s.
Change in Post Occlusive Reactive Hyperemia (PORH)pre-treatment baseline and following 12 weeks sub-acute whole-body vibrationChange from baseline PORH at 12 weeks. Measured by Laser Speckle Contrast Imager (Moor FLPI).
Change in IL-6pre-treatment baseline and following 12 weeks sub-acute whole-body vibrationchange from baseline concentrations of Interleukin 6 (IL-6) obtained via blood draw at 12 weeks.

Countries

United States

Contacts

Primary ContactJacob Looney, MS
jlooney@augusta.edu7067215483
Backup ContactRyan Harris, PhD
ryharris@augusta.edu7067215998

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026