Occupational Exposure to Whole Body Vibration Among U.S. Military Veterans: Acute and Chronic Contributions to Musculoskeletal Disorders and Spine-Area Pain

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-45
SponsorMilwaukee VA Medical Center

About this trial

Significance to VA: There is a lack of prospective longitudinal studies investigating the relationship between risk factors to Veterans and development and progression of musculoskeletal (MSK) spine injury and pain. Military operational exposure to whole body vibration (WBV) is known to contribute to MSK disorders and pain. Our preliminary studies identified accelerated lumbar and cervical spine degenerative changes in military fighter pilots and helicopter aircrew compared to age- and sex-matched civilian controls. Those changes were likely associated with WBV that military aircrew experience during flight training, primarily affected intervertebral discs (IVDs) and endplates, were associated with neck and back pain symptoms and reduced functional capacity, and are likely to lead to lifelong spine-related issues. Therefore, these aircrew, and other military personnel that experience occupational WBV, are likely to enter the VA Healthcare system with pre-existing degenerative changes and spine-related pain symptoms that can progress over time. Similarly, many Veterans enter civilian occupations that involve WBV such as truck drivers and heavy equipment operators that may also have detrimental effects to the spine and lead to spine-related pain. Development of informed interventions and treatment protocols requires a mechanistic understanding of how the spine is acutely and chronically affected by occupational WBV from both structural and physiological perspectives. Innovation and Impact: Novel multi-parametric application of noninvasive magnetic resonance imaging (MRI) techniques such as arterial spin labeling (ASL), T2\* decay from ultra short TE, and diffusion MRI can provide early objective indications of endplate degenerative state and IVD hydration and perfusion, and novel application of upright MR imaging allows for gravitational loading of the IVD while observing segmental and region IVD fluid distribution and transport patterns. Specific Aims: The goal of the proposed effort is to characterize the effects of previous military and current civilian occupational WBV on IVD and endplate health and degeneration (Aim 1), and segmental and regional IVD fluid distribution and transport differences (Aim 2). The endplates contain vasculature that permits IVD fluid exchange and may be linked to IVD fluid dynamics. We propose looking for connections between segmental and regional IVD fluid dynamics, degenerative state of the associated endplates, and WBV exposure (acute-controlled and longitudinal-occupational). Finally, we propose evaluating the impact of body hydration state on IVD fluid distribution and transport following acute (30 min) controlled WBV (Aim 3). Cumulatively, these results inform population-specific preventative measures to preserve endplate health for Veterans in occupations that present with WBV and identify potential areas for further research and targeted treatment of MSK disorders and MSK pain. Methodology: This study will explore acute and chronic changes to the structure and physiology of the spine by enrolling Veterans with prior military or current civilian occupation that involves daily WBV. Advanced MRI sequences will identify endplate sclerosis and physiological changes including disc hydration and perfusion. Acute effects of WBV will be assessed using pre/post MRI scans with experimental WBV. Path to translation/Implementation: Our existing relationships with VA clinicians, including spine surgeons, physical medicine and rehabilitation, and pain medicine, will ensure VA patient applicability of these findings and will help to translate any outcomes from this research and future studies directly into patient care.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

English speaking; Male/Female Veterans age 20-45 years; BMI < 30; ability to sit upright for 60 mins; ability to drive to Deerfield, IL; ambulatory

Disqualifiers

Previous spinal surgery; conditions/diseases associated with altered pain perception including neurological diseases (e.g., multiple sclerosis, trigeminal neuralgia, central sensitization), major psychiatric disorders, diabetes, neoplasm and cardiovascular disorders, chronic widespread pain diagnosis, pregnant women, MRI contraindications.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Water

    Other intervention

    Aim 3 will evaluate the effect of hydration and dehydration on acute whole body vibration response of the lumbar spine endplate and intervertebral disc.

Treatment groups

112 Participants
are divided into 3 treatment groups
Group A: Longitudinal effects of current or prior whole body vibration.No intervention 0 interventions
Group B: Determine how lumbar disc fluid flow is acutely affected by whole body vibratiNo intervention 0 interventions
Group C: Effect of hydration on lumbar spine response to whole body vibrationExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Occupational Whole Body Vibration History

We will use questionnaires to quantify each subject's history with regard to occupational whole body vibration. Groups will include subjects that had whole body vibration while in the military, subjects that have current occupations with whole body vibration, and subjects that have not significant history of whole body vibration.

Time frame
Whole body vibration questionnaires will be provided at the time of enrollment and immediately prior to each MRI scan.
2

Oswestry Disability Index

Patient-reported outcome measure that assesses the degree to which low back pain impacts a person's daily functioning. The questionnaire consists of 10 sections (pain intensity, personal care, lifting, walking, sitting, standing, sleeping, sex life, social life, traveling). Each section has 6 statements scored 0-5; patient selects the statement that best describes them.

Time frame
ODI will be collected at the time of enrollment and again immediately prior to each MRI scan.

Secondary outcomes

Other outcomes

Sponsors and contacts

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Milwaukee VA Medical Center

Lead sponsor

Medical College of Wisconsin

Collaborator

Indiana University

Collaborator

VA Office of Research and Development

Collaborator

Naval Aeromedical Research Unit, Dayton

Collaborator

This trial is not recruiting at the moment. You can still explore other options: