Back to search results
NCT07643207

Wearable Spine Assessment in Adults With and Without Low Back or Neck Pain

Active, Not Recruiting
Not specifiedAges 18–65Observational
Ashkan Vaziri
~20 participants
Updated 2026-06-17 on ClinicalTrials.gov

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Group discrimination between control/low back pain/neck pain - Peak lumbar flexion range of motion
Measured over Baseline Visit
+4 more outcomes measured

Conditions

Low Back Pain
Neck Pain

Explore related trials

Lower Back PainNeck Pain

Where it's being run

1 sites across 1 states
Massachusetts1

Who to contact

This trial hasn't published a contact. View it on ClinicalTrials.gov

Do you actually qualify for this trial?

Add a private profile and we'll compare every criterion below against your situation — and tell you which ones are met, uncertain, or excluding.

Check eligibility for this trial ~2 min · HIPAA-protected · delete anytime
Eligibility criteria

Inclusion

Male or female, aged 18-65 years
Fluent in English (able to speak and read)
Ambulatory without the need for a walking aid
Able to independently perform all study activities safely, as determined by the investigator
Willing and able to provide informed consent and comply with all study procedures
Self-reported low back or neck pain present for at least 4 weeks (subacute or chronic), with current Numeric Pain Rating Scale (NPRS) score of 3 or higher in the past 7 days
No history of spine surgery within the past 12 months

Exclusion

History of spine fracture, spinal deformity (e.g., scoliosis with Cobb angle \> 25°), or spinal cord injury
Active radicular signs requiring imaging or specialist referral, as determined by the investigator
Neurological, vestibular, or musculoskeletal condition that would interfere with safe performance of the study tasks
Pregnant individuals
Skin condition or adhesive sensitivity precluding sensor application
Body mass index (BMI) \< 18 kg/m² or \> 40 kg/m²
Inability to provide informed consent or comply with study procedures

What this trial measures

  • Group discrimination between control/low back pain/neck pain - Peak lumbar flexion range of motionBaseline Visit

    AxiSens system shall discriminate between groups based on peak lumbar flexion range of motion and lumbopelvic coordination ration during the Fingertip to Floor test.

  • Group discrimination between control/low back pain/neck pain - Peak cervical flexion range of motionBaseline Visit

    AxiSens system shall discriminate between groups based on peak cervical flexion range of motion and cervicothoracic coordination ration during the Chin to Chest test.

  • Group discrimination between control/low back pain/neck pain - Angular variabilityBaseline Visit

    AxiSens system shall discriminate between groups based on angular variability of the sagittal and frontal planes during the Trunk Stability test in eyes open and eyes closed conditions.

  • Group discrimination between control/low back pain/neck pain - Cervical flexor endurance timeBaseline Visit

    AxiSens system shall discriminate between groups based on endurance time during the Cervical Flexor Endurance test.

  • Group discrimination between control/low back pain/neck pain - Five times sit-to-stand completion timeBaseline Visit

    AxiSens system shall discriminate between groups based on completion time during the five times sit-to-stand test.