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Effects of Hip Abductor and External Rotator Strength Training in Patients With Patellofemoral Pain Syndrome

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00736736
Enrollment
85
Registered
2008-08-18
Start date
2008-03-31
Completion date
Unknown
Last updated
2008-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patellofemoral Pain Syndrome

Brief summary

The first purpose was to compare the difference between leg press exercise(LPE) and additional hip abductor and external rotator muscle strength training to leg press exercise(LPE+HAE) in muscle strength, hip kinematics during step down, pain severity and function for patients diagnosed with patellofemoral pain syndrome. The second one was to discover the relationship between the change in muscle strength performance and the difference of hip joint kinematics post treatment.

Interventions

OTHERAdditional Hip Muscle Strengthening to Leg Press Exercise

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
19 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* Patellofemoral pain syndrome ( Bilateral or unilateral) * Special tests: crepitus during compression test, patellar grind test (Clarke's sign), pain during compression test, palpation ( at least 2 ) * Below 50 years old * Pain :after long sitting, up/down stair, squat, kneeling, running & jumping ( at least 2 ) * Pain duration at least 1 month * At least 1 item of PSS score more than 3 cm

Exclusion criteria

* Knee operation * Central or peripheral neurological deficits * Obvious knee joint or lower extremity malalignment * People involved in competitive sports * PSS sub-scale pain experienced last week more than 8cm * Have been taking anti-inflammatory drugs , received anti-inflammatory injection or received other therapy for past 3 months

Design outcomes

Primary

MeasureTime frame
Muscle Strength by hand-held dynamometry, hip joint kinematics during step down by electromagnetic motion tracking system (FASTRAK, Polhemus ), pain severity by PFPS pain severity scale (PSS), functional performance by Anterior Knee Pain Scale(AKP).Pre and Post 8 weeks of exercise

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026