- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica 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
Panoramica dello studio
Stato
Condizioni
Intervento / Trattamento
Descrizione dettagliata
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.
Tipo di studio
Iscrizione
Fase
- Fase 2
- Fase 1
Contatti e Sedi
Luoghi di studio
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Taipei, Taiwan, 100
- Reclutamento
- School and Graduate Institute of Physical Therapy, National Taiwan University
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Contatto:
- Mei-Hwa Jan
- Numero di telefono: 886-2-33228138
- Email: mhjan@ntu.edu.tw
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
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
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione incrociata
- Mascheramento: Separare
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
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muscle strength
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VAS worst
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proprioception
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functional performance
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Collaboratori e investigatori
Investigatori
- Direttore dello studio: Mei-Hwa Jan, Kinesiology Lab, School and Graduate Institute of Physical Therapy, National Taiwan University
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Inizio studio
Completamento dello studio (Anticipato)
Date di iscrizione allo studio
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Stima)
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Stima)
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- 200611006R
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