Wearable Spine Health System for Military Readiness

Sponsor
Ohio State University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05944354
Collaborator
United States Department of Defense (U.S. Fed)
400
10
123.3
40
0.3

Study Details

Study Description

Brief Summary

The goal of this observational trial is to compare the health history and motion capabilities of participants with low back pain disorders to participants with healthy spines. The main question[s] it aims to answer are to:

  1. Primary outcomes of this research effort include the development of composite measures or digital biomarkers to track functional recovery over time and predict duty or work status outcomes (return-to-full duty/work, limited duty/work restrictions or medical discharge/long-term disability).

  2. Secondary outcomes of this research effort include characterization of motion assessment utility to predict reinjury risk and evaluate intervention effectiveness. In addition, exploratively, the investigators will determine biopsychosocial profiles of low back pain, and neck pain military populations to identify low back and neck pain phenotypes.

Participants will complete questionnaires and wear a motion monitor that will assess the participant's back and/or neck. This session will be approximately 40-70 minutes. The research team will follow up with participants at 6 week, 6 months, and 1 year to complete a short series of questionnaires and a motion assessment test.

Condition or Disease Intervention/Treatment Phase

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    400 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Wearable Spine Health System for Military Readiness
    Actual Study Start Date :
    Sep 23, 2022
    Anticipated Primary Completion Date :
    Dec 31, 2032
    Anticipated Study Completion Date :
    Dec 31, 2032

    Arms and Interventions

    Arm Intervention/Treatment
    Low Back Pain

    Subjects with Low Back Pain

    Neck Pain

    Subjects with Neck Pain

    Control

    Subjects with healthy spines, who have no neck or low back pain

    Outcome Measures

    Primary Outcome Measures

    1. Predict Work Status [2030]

      To track functional recovery over time that can predict duty or work status.

    Secondary Outcome Measures

    1. Predict Reinjury Risk [2030]

      To track reinjury risk and evaluate intervention effectiveness to predict reinjury risk.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 64 Years
    Sexes Eligible for Study:
    All
    Inclusion Criteria:

    Control Cohort

    • Ages 18-64

    • Able to stand for at least 25 minutes

    • Able to speak, read, and understand English

    Low Back Pain Cohort

    • Age 18-64

    • Able to stand for at least 15 minutes

    • Able to speak, read, and understand English

    • Within the last 3 months, an episode of low back pain lasting longer than 7 days and/or seeing a health care provider for low back pain and/or on duty/work restriction due to low back pain.

    Neck Pain Cohort

    • Ages 18-64

    • Able to stand for at least 15 minutes

    • Able to speak, read, and understand English

    • Within the last 3 months, an episode of neck pain lasting longer than 7 days and/or seeing a health care provider for neck pain and/or on duty/work restriction due to neck pain.

    Exclusion Criteria:

    Control Cohort

    • Known pregnancy

    • Within the last 3 months, back or neck pain lasting longer than 7 days and/or seeing a health care provider for low back or neck pain and/or on duty/work restriction due to low back or neck pain.

    • Actively being treated by a medical provider for concussion or traumatic brain injury

    • Known severe spine curvature or deformity requiring medical treatment (e.g. scoliosis)

    • Has been diagnosed by a medical provider with severe vertigo, fainting, narcolepsy, or balance disorders with high risk for falling

    • Any known fractures within the last 3 months that will interfere with the motion assessment

    • History of spine fracture

    • Current condition requiring a bracing or immobilization of the spine

    • History of spine surgery (e.g. fusion, micro-discectomy, or artificial disc replacement)

    • History of brain or spine cancer

    • Currently or within the last 90 days, been treated for cancer with chemotherapy or radiation therapy

    • Known severe bone loss or osteoporosis requiring medical treatment and physician-recommended physical restrictions

    • Current open wounds on the body where the harnesses will be placed on the neck, head, back, or hips

    • Current osteomyelitis or spine infection

    • Any other reason that a treating physician, researcher, or participant determines it is unsafe for a patient to perform test

    Low Back Pain Cohort

    • Known pregnancy

    • Current low back pain is the result of a traumatic injury (wreck, fall, etc.) that occurred within the last 3 months OR is positive for spine instability with imaging

    • Has spinal fusion across 4 or more lumbar disc levels

    • Currently being treated by a medical provider for concussion or traumatic brain injury

    • Known severe spine curvature or deformity requiring medical treatment (e.g. scoliosis)

    • Has been diagnosed by a medical provider with severe vertigo, fainting, narcolepsy, or balance disorders with high risk for falling

    • Any known fractures within the last 3 months that will interfere with the motion assessment

    • Any known spinal instability or spine fractures within the last 6 months

    • Current condition requiring a bracing or immobilization of the spine

    • History of brain or spine cancer

    • Currently or within the last 90 days, been treated for cancer with chemotherapy or radiation therapy

    • Known severe bone loss or osteoporosis requiring medical treatment and physician-recommended physical restrictions

    • Current open wounds on the body where the harnesses will be placed on the back or hips

    • Current spine infection or osteomyelitis

    • Any other reason that a treating physician, researcher, or participant determines it is unsafe for participant to perform test

    Neck Pain Cohort

    • Known pregnancy

    • Current neck pain is the result of a traumatic injury (wreck, fall, etc.) that occurred within the last 3 months OR is positive for spine instability with imaging

    • Has spinal fusion across 4 or more cervical disc levels

    • Has an occipital-cervical fusion

    • Currently being treated by a medical provider for concussion or traumatic brain injury

    • Known severe spine curvature or deformity requiring medical treatment (e.g. scoliosis)

    • Has been diagnosed by a medical provider with severe vertigo, fainting, narcolepsy, or balance disorders with high risk for falling

    • Any known fractures within the last 3 months that will interfere with the motion assessment

    • Any known spinal instability or spine fractures within the last 6 months

    • Current condition requiring a bracing or immobilization of the spine

    • History of brain or spine cancer

    • Currently or within the last 90 days, been treated for cancer with chemotherapy or radiation therapy

    • Known severe bone loss or osteoporosis requiring medical treatment and physician-recommended physical restrictions

    • Current open wounds on the body where the harnesses will be placed on the neck or head

    • Current spine infection or osteomyelitis

    • Any other reason that a treating physician, researcher, or participant determines it is unsafe for participant to perform test

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Luke Air Force Base Luke Air Force Base Arizona United States 85309
    2 Schriever Space Force Base Colorado Springs Colorado United States 80912
    3 Peterson Space Force Base Colorado Springs Colorado United States 80914
    4 Eglin Air Force Base Eglin Air Force Base Florida United States 32542
    5 Uniformed Services University Bethesda Maryland United States 20814
    6 Holloman Air Force Base Holloman Air Force Base New Mexico United States 88330
    7 Seymour-Johnson Air Force Base Seymour Johnson Air Force Base North Carolina United States 27530
    8 The Ohio State University Columbus Ohio United States 43210
    9 Wright-Patterson Air Force Research Laboratory Wright-Patterson Air Force Base Ohio United States 45433
    10 Joint Base Langley- Eustis Air Force Base Langley Air Force Base Virginia United States 23665

    Sponsors and Collaborators

    • Ohio State University
    • United States Department of Defense

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    William Marras, Principal Investigator, Ohio State University
    ClinicalTrials.gov Identifier:
    NCT05944354
    Other Study ID Numbers:
    • 2022X0054
    First Posted:
    Jul 13, 2023
    Last Update Posted:
    Jul 13, 2023
    Last Verified:
    Jul 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 13, 2023