The Spine Phenome Project

Sponsor
Ohio State University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05776771
Collaborator
United States Department of Defense (U.S. Fed), National Institutes of Health (NIH) (NIH), National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) (NIH)
10,500
1
120.4
87.2

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 composite measures that differentiate between control and patient populations, predict injury or reinjury risk, identify low back and neck pain patient phenotypes, and evaluate treatment effectiveness.

  2. Secondary outcomes of this research effort include an assessment of wearable motion sensor accuracy, characterization of motion assessment utility, biopsychosocial profiling of control and low back and neck pain patient populations, and differentiation of sincere and insincere motion assessment efforts.

Participants will complete questionnaires and wear a motion monitor that will assess your back and/or neck. This session will be approximately 40-70 minutes. The research team will follow up with participants at 3 month, 6 months, 1 year, 2 years, 5 years 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 :
    10500 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    The Spine Phenome Project: Enabling Technology for Personalized Medicine
    Actual Study Start Date :
    Dec 18, 2020
    Anticipated Primary Completion Date :
    Dec 31, 2030
    Anticipated Study Completion Date :
    Dec 31, 2030

    Arms and Interventions

    Arm Intervention/Treatment
    Low Back Pain

    Subjects with Low Back Pain

    Neck Pain

    Subjects with Neck Pain

    Control/Insincere

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

    Outcome Measures

    Primary Outcome Measures

    1. Idenify Patient Phenotypes [2030]

      Identify low back and neck pain patient phenotypes that can assist with idenifying composite measures that differentiate between control and patient populations, predict injury or reinjury risk, and evaluate treatment effectiveness.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes

    Controls/Insincere

    Inclusion Criteria

    • Age 18 and older

    • Able to stand for 20 minutes

    • Able to speak, read, and understand English

    Exclusion criteria:
    • Known pregnancy

    • Currently seeing or planning to see a medical provider for low back or neck pain

    • History of chronic low back or neck pain lasting longer than 3 months

    • Blind or severe uncorrected vision problems that prevent participant from reading a tablet or laptop screen

    • Deaf or hearing problems that prevent the participant from hearing verbal instructions

    • Actively being treated by a medical provider for concussion

    • Known severe spinal 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 immobilization or bracing 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 osteoporosis requiring medical treatment and physician-recommended physical restrictions

    • Current open wounds or medical device entry points where the harnesses will be placed on the neck, 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 Patients

    Inclusion Criteria

    • Age 18 and older

    • Currently seeking medical consult with primary complaint of low back pain

    • Able to speak, read, and understand English

    • Able to stand for 10 minutes

    Exclusion criteria:
    • Known pregnancy

    • Blind or severe uncorrected vision problems that prevent participant from reading a tablet or laptop screen

    • Deaf or hearing problems that prevent the participant from hearing verbal instructions

    • 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.

    • Actively being treated by a medical provider for concussion

    • Known severe spinal 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 spine fractures within the last 6 months

    • Known unstable spondylolisthesis (i.e. standing 3mm of movement on flexion/extension film)

    • Current condition requiring immobilization of the spine

    • History of brain or spine cancer

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

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

    • Current open wounds or medical device entry points where the harnesses will be placed on the 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

    Neck Pain Patients

    Inclusion Criteria

    • Age 18 and older

    • Currently seeking medical consult with primary complaint of neck pain

    • Able to speak, read, and understand English

    • Able to stand for 10 minutes

    Exclusion criteria:
    • Known pregnancy

    • Blind or severe uncorrected vision problems that prevent participant from reading a tablet or laptop screen

    • Deaf or hearing problems that prevent the participant from hearing verbal instructions

    • 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 or an occipital-cervical fusion.

    • Actively being treated by a medical provider for concussion

    • Known severe spinal 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 spine fractures within the last 6 months

    • Known unstable spondylolisthesis (i.e. standing 3mm of movement on flexion/extension film)

    • Current condition requiring immobilization of the spine

    • History of brain or spine cancer

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

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

    • Current open wounds or medical device entry points where the harnesses will be placed on the neck or back

    • 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

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 The Ohio State University Wexner Medical Center Columbus Ohio United States 43210

    Sponsors and Collaborators

    • Ohio State University
    • United States Department of Defense
    • National Institutes of Health (NIH)
    • National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)

    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:
    NCT05776771
    Other Study ID Numbers:
    • 2020H0250
    • 4UH3AR076729-02
    First Posted:
    Mar 20, 2023
    Last Update Posted:
    Mar 20, 2023
    Last Verified:
    Feb 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 Mar 20, 2023