Clinical Trials Directory

Trials / Completed

CompletedNCT01332110

Treatment for Patellofemoral Pain Syndrome Using Footwear

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

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
36 (actual)
Sponsor
University of Calgary · Academic / Other
Sex
All
Age
18 Years – 50 Years
Healthy volunteers
Not accepted

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.

Conditions

Interventions

TypeNameDescription
DEVICEKnee abduction moment-reducing footwearPatients in each study group will be asked to run using their assigned footwear at least 3 times per week (minimum 15 km per week) for six weeks. Each patient will document their perceived knee pain each week throughout the six week intervention.

Timeline

Start date
2011-06-01
Primary completion
2012-01-01
Completion
2012-08-01
First posted
2011-04-08
Last updated
2014-02-19

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT01332110. Inclusion in this directory is not an endorsement.