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Completed

NCT Number: NCT03167671

The Effect of AposTherapy on Pain and Function in a Non Specific Low Back Pain

AposTherapy is a home based exercise program utilizing footwear that causes exercise with normal activity that may significantly improve function in patients with back pain since patients with back pain have altered mechanics of motion contributing or due to the presence of the conditions. Capitalizing on the reported excellent adherence and clinical benefit of ApostTherapy in patients with significant knee and back pain, we propose to evaluate this as a conservative treatment that may supplant/supplement traditional pain medications and physical therapy in an at-risk urban inner city population.

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Key information

Age range

30 year–85 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Montefiore Medical Center

The Bronx, New York, 10467, United States

About this study

AposTherapy® is a home-based exercise program utilizing footwear that causes exercise with normal daily activity that may significantly improve function in patients with back pain in general, and specifically Axial Low Back Pain (NSLBP). Capitalizing on the reported excellent adherence and clinical benefit of Apos Therapy in patients with significant back pain, we propose to evaluate this as a conservative treatment that may supplant/supplement traditional pain medications and physical therapy in NSLBP population.

A possible potential use of AposTherapy® as a replacement for traditional physical therapy may yield a less costly, more effective therapy with better adherence. Problems with traditional therapy include poor patient adherence to both outpatient and home therapy programs, the added cost of travel (which may be more than $100 per session for ambulette or access-a-ride for eligible patients), and the lack of continuation in an ongoing exercise program[6-8], all of which can lead to relapse and need for retreatment. Additionally, access to physical therapy is limited for many patients since there are not enough available outpatient therapy services to meet the needs of all patients. Finding an alternative exercise program that will increase adherence, decrease total therapy visits, and improve patient's outcomes with decreased dependence on pain medications is a high priority from both patient care and cost management perspectives.

AposTherapy® potentially overcomes many of these issues by improving/modifying abnormal biomechanics (therefore decreasing pain), and providing an independent home-based exercise program utilizing footwear that causes exercise with normal activity by promoting perturbation. This biomechanical approach may significantly reduce pain and improve function in patients with nonspecific low back pain (NSLBP). Capitalizing on the reported excellent adherence and clinical benefit of AposTherapy® in patients with significant NSLBP, we propose to evaluate the biomechanical exercise (wearing an appropriately calibrated shoe at home for a prescribed amount of time each day) as a conservative treatment that may supplement or supplant traditional pain medications, interventional pain procedures and physical therapy in an at-risk urban inner city population with NSLBP.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • •Patients suffering from symptomatic axial lower back pain for at least 24 weeks.
  • Patients with VAS pain score of ≥3cm (measured at baseline).
  • Males and females between the ages of 30-85.
  • 17<BMI<40
  • Ambulatory and active patients that can participate in a rehabilitation program that includes daily walking
  • Stable medicine regimen (no recent changes to their pain medication within a month)
  • Able to walk at least 50 meters and scored positive on the STEADI test (Supp. 1)
  • Able to understand, read and sign the informed consent form
  • English or Spanish speaking

Exclusion criteria

  • •Patients suffering from active inflammatory joint disease.
  • Patients with diagnosis of neuromuscular disease.
  • Patients with more than 3 falls in the last 52 weeks, OR any balance related fall with an injury in the last 52 weeks.
  • Patients exhibiting a lack of physical or mental ability to perform or comply with the study procedure.
  • Patients with a history of pathological osteoporotic fracture
  • Patients with referred pain consistent with radicular etiology
  • Patients with generalized body pain (both upper and lower extremities).
  • No spine surgery within 24 weeks.
  • No image guided lumbar intervention in the past 8 weeks.
  • No major cardiovascular comorbidities (able to enroll in an active exercise program)
  • Patient started on lipid lowering medication in last 12 weeks
  • Any change in blood pressure medications
  • No recent physical therapy for the back. (within the last 12 weeks)
  • No active heart disease (ischemia or heart failure admissions within 24 weeks) and no active COPD (exacerbation within 24 weeks)
  • No active malignancies on ongoing treatment
  • Patient with neurological gait pattern.
  • Patient requiring assistive device during gait analysis.

Treatment and study plan

AposTherapy

Device

AposTherapy® is a home-based exercise program utilizing footwear that causes exercise with normal daily activity

Traditional Physical therapy

Other

Up to 20 sessions of traditional physical therapy

Primary outcomes

  1. Function

    Time frame: 1 Year

    Improvement in back pain measured and assessed with the Oswestry Disability Index (ODI).

Secondary outcomes

  1. PROMIS (Patient-Reported Outcomes Measurement Information System) Pain Interference and Physical Function

    Time frame: 1 year

    Pain and Function measured through PROMIS short forms

  2. Pain medication consumption

    Time frame: 1 year

    medication consumption

  3. Quality of life survey

    Time frame: 1 year

    Quality of life assessed with Short Form Health Survey questionnaire

  4. Gait assessment

    Time frame: 1 year

    objective analysis of patients' gait assessed with a pressure mat to demonstrate stride length, velocity, and symmetry.

  5. 6-min walk test

    Time frame: 1 year

    objective assessment using maximum distance comfortably walked in 6 minutes on a 100 foot closed course

  6. Dynamic balance

    Time frame: 1 year

    Measured by Berg balance test assessed with a questionnaire

  7. Static balance

    Time frame: 1 year

    functional reach test assessed by physically testing the patient with a standardized set of instructions

  8. Blood pressure

    Time frame: 1 year

    Change in blood pressure , physiological parameter

  9. resting heart rate

    Time frame: 1 year

    change in resting heart rate , physiological parameter

  10. Overall activity

    Time frame: 1 year

    overall activity measured as daily steps, through wristband devices

  11. sleep patterns

    Time frame: 1 year

    Total sleep time measured in minutes through wristband activity monitor (FitBit) measured over one week

  12. Visual Analog Scale (VAS) for pain measurement

    Time frame: 1 year

    questionnaire

  13. Medication Consumption

    Time frame: 1 year

    Track increase or decrease in Medication consumption- assessed through patient interview and patent report

  14. Medication Costs

    Time frame: 1 year

    Calculate monetary savings in Medication Costs- assessed through patient interview and prevailing market cost information

  15. Hospitalization utilizations

    Time frame: 1 year

    Calculate the increase/decrease in hospital facility utilization - assessed with patient interview and health records.

Sponsors and collaborators

Lead sponsor

Montefiore Medical Center

Other

Collaborators

  • Apos Medical and Sports Technology Ltd.

Registry information

Official study title

The Effect of AposTherapy on Pain and Function in a Non Specific Low Back Pain Population. A Randomized Controlled Trial

Acronym: AposBack

Important dates

Study start
2017
Primary completion
2023
Study completion
2023
First posted
May 30, 2017
Registry last updated
May 6, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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