Comparison of The Clinical Effects Between Different Physical Therapy Tools in Patellofemoral Pain Patients

NCT ID: NCT00451347

Last Updated: 2007-03-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

PHASE1/PHASE2

Total Enrollment

90 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-11-30

Study Completion Date

2008-08-31

Brief Summary

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Objectives:The purpose of this study was to investigate the different effects among the quadriceps strength training, taping, and stretching exercise of iliotibial band in patients with patellofemoral pain syndrome by randomized control trial study.

Method:An observer blind, prospective, factorial design randomized controlled trail. 90 young adults with patellofemoral pain syndrome were randomly allocated into one of three treatment groups: (1) Quadriceps strength training, (2) taping, and (3) stretch. Each group received treatment for 8 weeks.

Hypothesis:Patients in quadriceps strength training group may get most outcomes in three groups

Detailed Description

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Introduction:Patellofemoral pain syndrome ( PFPS ) is a common knee disorder. Factors that cause patellofemoral pain include: over use, soft tissue imbalance, and malalignment of lower extremity. Patients with patellofemoral pain, caused by soft tissue imbalance was thought to be favorite to receive physical therapies. Clinically, physical therapies for patients with PFPS are including: Quadriceps strength training, taping, and stretching exercise. The aforementioned treatment tools showed different effect mechanism. However, there were few clinical studies to compare the clinical effects among the aforementioned three treatment tools. The purpose of this study was to investigate the different effects among the quadriceps strength training, taping, and stretching exercise of iliotibial band in patients with patellofemoral pain syndrome by randomized control trial study.

Methods:An observer blind, prospective, factorial design randomized controlled trail. 90 young adults with patellofemoral pain syndrome were randomly allocated into one of three treatment groups: (1) Quadriceps strength training, (2) taping, and (3) stretch. Each group received treatment for 8 weeks.

Outcome measures were including visual analog scales for worst pain, active-active joint reposition error test, the Chinese version of the Western Ontario and McMaster Universities Osteoarthritis Index, and one repetition maximum recorded at baseline and after the interventions for 8 weeks.

Conditions

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Patellofemoral Pain Syndrome

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Interventions

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Quadriceps strength training

Intervention Type DEVICE

Taping

Intervention Type DEVICE

Home exercise

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* Anterior or retropatellar knee pain present during at least two of the following: ascending/descending stairs, hopping, running, squatting, kneeling, and prolong sitting
* Insidious onset of symptom unrelated to a traumatic incident
* Pain on palpation of peripatella
* VAS\>3
* Age \<50 years old
* Symptoms sustained for more than 1 month

Exclusion Criteria

* Over activity: athlete, infatry
* Patients with meniscal lesion, ligamentous instability, patellar tendon pathology, radiation pain from spine, referred pain
* Neurological disease involved
Minimum Eligible Age

16 Years

Maximum Eligible Age

50 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Taiwan University Hospital

OTHER

Sponsor Role lead

Principal Investigators

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Mei-Hwa Jan

Role: STUDY_DIRECTOR

Kinesiology Lab, School and Graduate Institute of Physical Therapy, National Taiwan University

Locations

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School and Graduate Institute of Physical Therapy, National Taiwan University

Taipei, , Taiwan

Site Status RECRUITING

Countries

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Taiwan

Central Contacts

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Mei-Hwa Jan, Master

Role: CONTACT

886-2-33228138

Facility Contacts

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Mei-Hwa Jan

Role: primary

886-2-33228138

Other Identifiers

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200611006R

Identifier Type: -

Identifier Source: org_study_id

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