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Clinical Trials/NCT01332110
NCT01332110
Completed
Phase 1

Treatment for Patellofemoral Pain Syndrome Using Knee Abduction Moment-Reducing Footwear

University of Calgary1 site in 1 country36 target enrollmentJune 2011

Overview

Phase
Phase 1
Intervention
Not specified
Conditions
Patellofemoral Pain Syndrome
Sponsor
University of Calgary
Enrollment
36
Locations
1
Primary Endpoint
Knee joint internal abduction moments of force during running at 4m/s
Status
Completed
Last Updated
12 years ago

Overview

Brief Summary

Patellofemoral pain syndrome (PFPS) is the most common running injury and is believed to be associated with higher than normal knee joint loading. Footwear has been developed that may decrease these knee loads in healthy subjects, but their effects on patients with PFPS are unknown. In this study, we aim to test the effects of such footwear on patients with PFPS. We hypothesize that patients who receive the footwear intervention will show a decrease in knee joint loading, and consequently will show improvements in subjective levels of perceived knee pain over a period of six weeks compared to a control condition.

Registry
clinicaltrials.gov
Start Date
June 2011
End Date
August 2012
Last Updated
12 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Ryan Lewinson

Ryan T. Lewinson

University of Calgary

Eligibility Criteria

Inclusion Criteria

  • Male or Female between 18 and 45 years of age.
  • Have been diagnosed with patellofemoral pain syndrome (PFPS) by a physician.
  • Have nontraumatic unilateral and/or bilateral peripatellar or retropatellar knee pain.
  • Patellofemoral knee pain with and/or after activity.
  • Inactivity patellofemoral pain and/or stiffness, especially with sitting with knees held in flexed posture.
  • Peripatellar tenderness ± mild inferior patellar pole tenderness.
  • Run at least 15km per week.
  • Are heel-toe runners (as opposed to forefoot strikers).

Exclusion Criteria

  • Are currently, or have previously, participated in any other forms of treatment for their knee pain.
  • Significant articular or periarticular effusion or bursitis.
  • Significant joint line tenderness.
  • Intra-articular ligamentous instability.
  • Patellar apprehension.
  • Have undergone any form of knee surgery or arthroscopy.
  • Have any other neuromuscular, musculoskeletal or cardiovascular conditions

Outcomes

Primary Outcomes

Knee joint internal abduction moments of force during running at 4m/s

Time Frame: First day of joining the study

Motion analysis trials will be conducted on each subject with both the control and intervention footwear. Inverse dynamics calculations will reveal the internal joint loading for each subject. Knee joint moments will be compared within subjects for each footwear condition.

Secondary Outcomes

  • Change in subjective levels of perceived knee pain over six weeks(Upon initial recruitment to the study, and once per week for six weeks thereafter)

Study Sites (1)

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