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Effects of Home Base Whole-body Vibration in Osteoarthritis. (VIBE-Rx2)

Pilot Investigation on the Effects of Sub Acute (12 Week) Home Base Whole-body Vibration Training in Osteoarthritis.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06058169
Enrollment
30
Registered
2023-09-28
Start date
2025-04-25
Completion date
2026-09-01
Last updated
2026-05-14

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

Conditions

Osteo Arthritis Knee, Whole Body Vibration

Brief summary

The purpose of this proposal is to understand how the Vibrant Health Ultimate whole-body vibration (WBV) machine affects pain and inflammation in older adults. The investigators' hypothesize that sub-acute (12 weeks) WBV will lead to improvement in the level of knee pain and improve vascular function via a decrease in systemic inflammation.

Detailed description

Knee osteoarthritis (KO) is a leading cause of disability and medical cost. Whole body vibration (WBV) has emerged as an exercise alternative that may be more tolerable than traditional forms of exercise, such as treadmill walking/running or cycling. Similar to traditional exercise, research supports that WBV can be very beneficial for your health. In fact, a single bout of WBV increases circulating concentrations of inflammatory markers. WBV is safe and effective, WBV training has been conducted in obesity, elderly, patients with diabetes, patients with lung disease, as well as patients with knee osteoarthritis.

Interventions

Participants will be given a personal vibration plate (equipped with stabilizing bars) to take home for training which will last for up 12 weeks. For this test the participant will be asked to stand on a vibration plate for up to 20 minutes. Participants will be instructed to remove any footwear and stand mid-center on the platform in a standing position with feet shoulder width apart. The participant will be asked to step on and off of the vibration plate. During the first four weeks, participants will be asked to complete 5-10 minutes of WBV per day, at least 4-5 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 15 minutes and/or reduce the duration of rest. Beginning at week 9, based on how the participant feels, the study team may adjust the WBV time/duration up to 20 minutes per session, 4-5 days per week.

Sponsors

Augusta University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
40 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* Symptomatic Osteoarthritic knee pain for at least 6 months. * Mean and women * Ages 40-75 years old

Exclusion criteria

* \<40 years old or \>75 years old * History of balance issues * History of falls * Epilepsy * Pregnancy * The use of whole-body vibration in the past 6 months * Previous knee surgery within last 3 years * Unable to stand for at least 20 minutes (for whole body vibration training)

Design outcomes

Primary

MeasureTime frameDescription
Change in Pain Pressure Threshold assessed using the Jtech Medical Echo Algometerpre-treatment baseline and following 12 weeks sub-acute whole-body vibrationchange from baseline pain pressure threshold at 12 weeks. Pain Pressure Threshold (PPT) will be assessed using the Jtech Medical Echo Algometer. PPT is used to measure deep muscular tissue sensitivity. The test determines the amount of pressure over a given area in which a steadily increasing non-painful pressure stimulus turns into an uncomfortable or painful pressure sensation. The subject will lie supine. An investigator will assess PPT at the following sites: a) 2 cm below the medial edge of the patella and b) 2 cm below the lateral edge of the patella. Using the 1 cm2 probe, the investigator will place it perpendicular to each site and apply pressure at a rate of 0.5 kg/cm2/s. Each trial will stop when the subject reports pain. The investigator will take 3 trials at each site; the average of the 3 trials, recorded in kg/cm2, will be used for statistical analysis.

Secondary

MeasureTime frameDescription
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 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

CONTACTJacob Looney, MS
jlooney@augusta.edu7067215483
CONTACTRyan Harris, PhD
ryharris@augusta.edu7067215998

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 15, 2026