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Comparing Rehabilitation Programs for Patellofemoral Pain Syndrome

Not Applicable
Completed
Conditions
Patellofemoral Pain Syndrome
Interventions
Other: Quad Progressive Resistive Exercises
Other: Hip Progressive Resistive Exercise
Registration Number
NCT00445224
Lead Sponsor
Timothy Uhl
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.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
33
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Quad Progressive Resistive ExercisesQuad Progressive Resistive ExercisesExercises targeting quadriceps musculature such as quadriceps isometric setting, terminal knee extensions, and straight leg raises that was progressed by increased resistance following typical progressive resistive exercise approach..
Hip Progressive Resistive ExercisesHip Progressive Resistive ExerciseExercises targeting hip musculature such as hip abduction and hip external rotation that was progressed by increased resistance following typical progressive resistive exercise approach.
Primary Outcome Measures
NameTimeMethod
Subjective Function by Lower Extremity Functional Scale Report FormBaseline, Mid-Intervention, and Post-Intervention
Visual Analog Pain Scale (Describing Worst Pain Felt During the Past Week)weekly

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

Visual Analog Pain Scale8 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 Outcome Measures
NameTimeMethod
Strength by Isometric DynamometerBaseline, Mid, and Post-Intervention
Neuromuscular Activity by Surface Electromyographical Amplitude During Stair DescentBaseline, Mid and Post-Intervention
Hip Abduction Strength8 week

Side lying Hip Abduction maximal muscular contraction with a hand held dynamometer

Objective Function by Step-down Task for 30 SecondsBaseline, Mid, and Post-Intervention

Trial Locations

Locations (1)

University of Kentucky

🇺🇸

Lexington, Kentucky, United States

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