Comparative Effects Of Clamshell And Short Arc Quadriceps Exercises In Patellofemoral Pain (CASCAPE-PFPS)
Comparative Effects Of Clam Shell Exercises And Short Arc Quadriceps Strengthening Exercises On Pain, Functional Disability And Quality Of Life In Patellofemoral Pain Syndrome
This is a research study to compare two different exercises for people who have patellofemoral pain syndrome. Patellofemoral pain syndrome means pain around or behind the kneecap, which is also called "runner's knee".
People in this study will be divided into two groups by chance. One group will do clamshell exercises. This exercise strengthens hip muscles. The other group will do short arc quadriceps exercises. This exercise strengthens thigh muscles near the knee. Both groups will do their exercises for the same number of weeks.
The main goal of this study is to see which exercise reduces knee pain better and helps patients do daily activities more easily. We will also check if quality of life improves after doing these exercises.
Pain level, knee function, and quality of life will be checked before starting exercises and again after finishing the exercise program.
The results may help doctors and physical therapists choose the best exercise for patients with kneecap pain.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
This randomized parallel-group clinical trial will compare the effectiveness of clamshell exercises versus short arc quadriceps strengthening exercises in patients diagnosed with patellofemoral pain syndrome.
Study Design: Participants meeting inclusion criteria for patellofemoral pain syndrome will be randomly allocated into two intervention groups.
Group 1 - Clamshell Exercise Group: Participants will perform clamshell exercises targeting hip abductors and external rotators, specifically gluteus medius and gluteus maximus muscles.
Group 2 - Short Arc Quadriceps Group: Participants will perform short arc quadriceps strengthening exercises focusing on quadriceps femoris muscle, with emphasis on vastus medialis obliquus activation.
Intervention Duration: Both groups will follow supervised exercise protocols for [X weeks]. Frequency and repetitions will be as per standard protocol.
Outcome Measures:
Primary: Pain intensity using Visual Analog Scale, Functional disability using Kujala Anterior Knee Pain Scale, Quality of Life using SF-36 questionnaire.
Assessments will be conducted at baseline, mid-intervention, and post-intervention to compare changes between the two exercise groups.
Hypothesis: Clamshell exercises targeting hip muscles may show superior effects on pain and function compared to short arc quadriceps exercises in PFPS patients.
Type d'étude
Inscription (Réel)
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
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Punjab Province
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Sargodha, Punjab Province, Pakistan, 40100
- Tehsil Headquarter Hospital, Bahlwal
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
Accepte les volontaires sains
La description
Inclusion Criteria:
Patients diagnosed with Patellofemoral Pain Syndrome Age between 18-40 years. Male and female participants Presence of anterior knee pain for at least 4 weeks Pain aggravated by activities such as stair climbing, squatting, running, or prolonged sitting Willingness to participate and provide informed consent
Exclusion Criteria:
History of knee surgery or fracture around the knee joint Ligament injuries (e.g., ACL, PCL tears) or meniscal injuries Presence of other knee conditions (e.g., osteoarthritis, patellar dislocation). Neurological disorders affecting lower limb sensations and gait Current participation in any other physiotherapy or rehabilitation program Systemic inflammatory conditions (e.g., rheumatoid arthritis). Cognitive impairment or inability to follow instructions/attend sessions. Use of long-term steroids, strong analgesics, or anti-inflammatory medications.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Tripler
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Expérimental: Clamshell Exercise Group
Participants in this group will perform clamshell exercises targeting hip abductors and external rotators.
Exercise includes side-lying hip abduction with knees bent at 45 degrees, focusing on gluteus medius and gluteus maximus strengthening.
Sessions will be supervised by physical therapist for [X weeks], [frequency per week].
|
A hip strengthening exercise performed in side-lying position with hips and knees flexed.
Patient opens top knee like a clamshell while keeping feet together to strengthen gluteus medius and external rotators.
Autres noms:
|
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Expérimental: Short Arc Quadriceps Exercise Group
Participants in this group will perform short arc quadriceps strengthening exercises targeting quadriceps femoris muscle with emphasis on vastus medialis obliquus activation.
Exercise performed from 30 to 0 degrees knee extension in short arc range.
Sessions will be supervised by physical therapist for [X weeks], [frequency per week].
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A knee strengthening exercise performed in short range of motion from 30 degrees to full extension.
Patient extends knee against resistance while quadriceps muscle is activated, focusing on vastus medialis obliquus.
Autres noms:
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Change in Pain Intensity
Délai: Baseline and 12 weeks post-intervention
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Pain intensity will be assessed using Visual Analog Scale (VAS).
VAS is a 10cm horizontal line where 0 = no pain and 10 = worst pain imaginable.
Patients mark their current knee pain level.
Change in VAS score will be measured from baseline to post-intervention after completion of exercise program.
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Baseline and 12 weeks post-intervention
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Change in Knee Function
Délai: Baseline and 12 weeks post-intervention
|
Knee function will be assessed using Kujala Anterior Knee Pain Scale (AKPS).
AKPS is a 13-item questionnaire specific for patellofemoral pain syndrome.
Total score ranges from 0 to 100, where 100 = no limitation and 0 = maximum limitation.
Change in AKPS score will be measured from baseline to post-intervention.
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Baseline and 12 weeks post-intervention
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Change in Quality of Life
Délai: Baseline and 12 weeks post-intervention
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Quality of life will be assessed using Short Form-36 Health Survey (SF-36).
SF-36 includes 8 domains: physical functioning, role physical, bodily pain, general health, vitality, social functioning, role emotional, mental health.
Scores range from 0 to 100 for each domain.
Change in SF-36 scores will be measured from baseline to post-intervention.
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Baseline and 12 weeks post-intervention
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Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- GIU/REC/26-40
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Description du régime IPD
Délai de partage IPD
Critères d'accès au partage IPD
Type d'informations de prise en charge du partage d'IPD
- PROTOCOLE D'ÉTUDE
- SÈVE
- CIF
- RSE
Informations sur les médicaments et les dispositifs, documents d'étude
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