ClinicalTrials.Veeva

Menu

The Effect of AposTherapy on Knee Pain (AposKnee)

Montefiore Medicine Academic Health System logo

Montefiore Medicine Academic Health System

Status

Terminated

Conditions

Knee Osteoarthritis
Knee Pain

Treatments

Device: AposTherapy
Other: Traditional Physical Therapy

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT03171168
2015-4842

Details and patient eligibility

About

AposTherapy is a home based exercise program utilizing footwear that causes exercise with normal activity that may significantly improve function in patients with knee osteoarthritis since patients with knee osteoarthritis 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 OA, the investigators 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.

Full description

AposTherapy is a home-based exercise program utilizing footwear that causes exercise with normal daily activity that may significantly improve function in patients with knee pain in general, and specifically knee osteoarthritis (OA). Capitalizing on the reported excellent adherence and clinical benefit of Apos Therapy in patients with significant lower limb arthritis, the investigators propose to evaluate this as a conservative treatment that may supplant/supplement traditional pain medications and physical therapy in knee OA population.

A 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 (patients often do not complete the sessions and have very poor adherence (about 50-60%) to home therapy programs), 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, leading 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 with improving/modifying abnormal biomechanics (therefore decreasing pain), and a 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 knee OA. Capitalizing on the reported excellent adherence and clinical benefit of AposTherapy in patients with significant knee OA, the investigators 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 knee OA.

Enrollment

54 patients

Sex

All

Ages

40 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients suffering from symptomatic knee OA (uni/bi lateral) for at least six months, fulfilling the American College of Rheumatology (ACR) clinical criteria for OA of the knee, and having radiographically assessed OA of the knee according to the Kellgren and Lawrence scale.
  • Patients with a Visual Analog Scale (VAS) pain score of ≥3cm (measured at baseline).
  • Males and females between the ages of 40-75.
  • 17<BMI<40
  • Ambulatory and active patients that can participate in a rehabilitation program that includes daily walking
  • Stable medical regimen (no recent changes to the pain medication within a month)
  • Able to walk at least 50 meters and scored positive on the STEADI test
  • Able to understand, read and sign the informed consent form
  • English or Spanish speaking

Exclusion criteria

  • Patients suffering from acute septic arthritis.
  • Patients suffering from inflammatory joint disease such as rheumatoid arthritis.
  • Patients with diagnosis of avascular necrosis of the knee.
  • Patients with diagnosis of neuromuscular disease.
  • Patients with more than 3 falls in the last 12 months, OR any fall with an injury in the last 12 months.
  • 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 in the knees from back or hip joint symptoms.
  • Patients with severe back pain, ≥ 4 cm in visual analogue scale (0-10) [1] or radiating leg pain
  • Patients with generalized body pain (both upper and lower extremities, such as fibromyalgia
  • No major surgery to the affected limb and contralateral limb (e.g. no joint replacements or surgical fracture repair)
  • No major cardiovascular comorbidities (able to enroll in an active exercise program)
  • Patient started on lipid lowering medication in last 3 months
  • Any change in blood pressure medications
  • No recent physical therapy (no more recent than 6 months) on the affected limb
  • No active heart disease (ischemia or heart failure admissions within 6 months) and no active Chronic Obstructive Pulmonary Disease (COPD) (exacerbation within 6 months)
  • No active malignancies on ongoing treatment
  • Patient with neurological gait pattern
  • Patient requiring assistive device during gait analysis.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

54 participants in 2 patient groups

Traditional Physical Therapy
Active Comparator group
Description:
Participants will have traditional physical therapy up to 20 sessions, up to two sessions per week. This will involve exercise and modalities as decided by the therapists and medical providers. Participants will have a home exercise program for the remainder of the year.
Treatment:
Other: Traditional Physical Therapy
AposTherapy
Experimental group
Description:
Participants will have AposTherapy instead of traditional physical therapy over the course of one year. This will include 7 sessions of gait assessment and re-calibration with daily at home exercise with the device over the year.
Treatment:
Device: AposTherapy

Trial documents
1

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2025 Veeva Systems