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Core Stabilization for the Treatment of Anterior Knee Pain

Not Applicable
Conditions
Patellofemoral Pain Syndrome
Interventions
Other: lower extremity training only
Other: core stabilization
Registration Number
NCT02123602
Lead Sponsor
Youngstown State University
Brief Summary

The investigators hypothesize that the use of trunk (core) stabilization exercises early in treatment combined with lower extremity exercises will enhance the outcome over lower extremity exercises alone in the treatment of young athletes with anterior knee pain.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
50
Inclusion Criteria
  • Subjects between 13-20 years of age clinically diagnosed with anterior knee pain.

  • Pain should be peripatellar and should include at least 3 of the following:

    1. experienced during or after activity
    2. prolonged sitting
    3. with stair climbing or descending
    4. squatting
    5. kneeling.
  • The subject should be active for at least 30 minutes per day.

Exclusion Criteria
  • Previous knee surgery
  • Signs and symptoms of a specific structural diagnosis not consistent with AKP such as meniscal, ACL, PCL, or collateral ligament tears, pain referral from hip or lumbar spine (determined during examination), traumatic patellar dislocation, an inability to adequately understand or communicate in English.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Lower extremity training onlylower extremity training onlyThis arm with receive 6 weeks of impairment based stretching and strengthening to restore function.
Core stabilizationcore stabilizationThis arm will receive 3 weeks of core stabilization training followed by 3 weeks of lower extremity stretching and strengthening as appropriate to address impairments noted in the examination and to progress function.
Primary Outcome Measures
NameTimeMethod
Lower extremity functional scale6 weeks

LEFS is a functional scale that estimates how much the subject's function is disrupted by their condition.

Secondary Outcome Measures
NameTimeMethod
Numeric pain rating scale6 weeks

The NPRS measures the subject's current knee pain

Kujala anterior knee pain scale6 weeks

The Kujala scale measures the amount and impact of anterior knee pain on the subject's life

Patient specific functional scale6 weeks

The PSFS rates subject's ability to do the 3 functional activities that are bothered the most by the knee pain

Trial Locations

Locations (1)

Poland Medical Center

🇺🇸

Poland, Ohio, United States

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