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Clinical Trials/NCT00445224
NCT00445224
Completed
Not Applicable

Comparison of Early Hip Strengthening to Early Quadriceps Strengthening in the Treatment of Females With Patellofemoral Pain

Timothy Uhl1 site in 1 country33 target enrollmentJanuary 2008

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Patellofemoral Pain Syndrome
Sponsor
Timothy Uhl
Enrollment
33
Locations
1
Primary Endpoint
Subjective Function by Lower Extremity Functional Scale Report Form
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

Patellofemoral pain syndrome (PFPS) is a common knee disorder affecting physically active people. Despite the growing base of support for the early introduction of hip strengthening exercises into the rehabilitation of PFPS, there have been few randomized clinical trials comparing isolated hip to isolated quadriceps strengthening. The purpose of this study is to determine how different exercises affect pain, strength, muscle activity, and function in female subjects with patellofemoral pain. The researchers hypothesize that females diagnosed with PFPS who initially participate in a hip strengthening program will report a greater perceived level of function, greater strength, less pain, and improved neuromuscular activity than those who participate in a progressive quadriceps strengthening intervention.

Detailed Description

Methods: Thirty-three females with PFPS will perform either initial hip strengthening (hip group) or initial quadriceps strengthening (quad group) for 4 weeks, prior to 4 weeks of a similar program of functional weight-bearing exercises. Self-reported pain, function, and functional strength were measured. Isometric strength was assessed for hip abductors, external rotators, and knee extensors. A mixed-model analysis of variance will be used to determine group differences over time.

Registry
clinicaltrials.gov
Start Date
January 2008
End Date
January 2010
Last Updated
9 years ago
Study Type
Interventional
Study Design
Crossover
Sex
Female

Investigators

Responsible Party
Sponsor Investigator
Principal Investigator

Timothy Uhl

Professor

University of Kentucky

Eligibility Criteria

Inclusion Criteria

  • anterior or retropatellar knee pain reported during at least 2 of the following activities: ascending and descending stairs, hopping and running, squatting, kneeling, and prolonged sitting
  • insidious onset of symptoms not related to trauma
  • pain with compression of the patella
  • pain on palpation of the patellar facets

Exclusion Criteria

  • symptoms present for less than one month
  • clinical evidence of other knee pathology
  • history of recent knee surgery within past one year
  • history of patellar dislocations or subluxations
  • current significant injury affecting other lower extremity joints

Outcomes

Primary Outcomes

Subjective Function by Lower Extremity Functional Scale Report Form

Time Frame: Baseline, Mid-Intervention, and Post-Intervention

Visual Analog Pain Scale (Describing Worst Pain Felt During the Past Week)

Time Frame: weekly

0 to 10 cm line with 0 representing no pain and 10 representing severe pain

Visual Analog Pain Scale

Time Frame: 8 week

Visual analog pain scale at end of intervention. 0 to 10 cm line with 0 representing no pain and 10 representing severe pain

Secondary Outcomes

  • Strength by Isometric Dynamometer(Baseline, Mid, and Post-Intervention)
  • Neuromuscular Activity by Surface Electromyographical Amplitude During Stair Descent(Baseline, Mid and Post-Intervention)
  • Hip Abduction Strength(8 week)
  • Objective Function by Step-down Task for 30 Seconds(Baseline, Mid, and Post-Intervention)

Study Sites (1)

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