- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT00451347
Comparison of The Clinical Effects Between Different Physical Therapy Tools in Patellofemoral Pain Patients
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
Studieöversikt
Status
Betingelser
Intervention / Behandling
Detaljerad beskrivning
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.
Studietyp
Inskrivning
Fas
- Fas 2
- Fas 1
Kontakter och platser
Studiekontakt
- Namn: Mei-Hwa Jan, Master
- Telefonnummer: 886-2-33228138
- E-post: mhjan@ntu.edu.tw
Studieorter
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Taipei, Taiwan, 100
- Rekrytering
- School and Graduate Institute of Physical Therapy, National Taiwan University
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Kontakt:
- Mei-Hwa Jan
- Telefonnummer: 886-2-33228138
- E-post: mhjan@ntu.edu.tw
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-
Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
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
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Crossover tilldelning
- Maskning: Enda
Vad mäter studien?
Primära resultatmått
Resultatmått |
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muscle strength
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VAS worst
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proprioception
|
functional performance
|
Samarbetspartners och utredare
Utredare
- Studierektor: Mei-Hwa Jan, Kinesiology Lab, School and Graduate Institute of Physical Therapy, National Taiwan University
Studieavstämningsdatum
Studera stora datum
Studiestart
Avslutad studie (Förväntat)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Uppskatta)
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- 200611006R
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