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
1 other identifier
interventional
34
1 country
1
Brief Summary
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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Nov 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 2, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 29, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
May 5, 2026
CompletedFirst Submitted
Initial submission to the registry
June 9, 2026
CompletedFirst Posted
Study publicly available on registry
June 12, 2026
CompletedJune 12, 2026
June 1, 2026
6 months
June 9, 2026
June 9, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change in Pain Intensity
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.
Baseline and 12 weeks post-intervention
Secondary Outcomes (2)
Change in Knee Function
Baseline and 12 weeks post-intervention
Change in Quality of Life
Baseline and 12 weeks post-intervention
Study Arms (2)
Clamshell Exercise Group
EXPERIMENTALParticipants 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 \[X weeks\], \[frequency per week\].
Short Arc Quadriceps Exercise Group
EXPERIMENTALParticipants 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 \[X weeks\], \[frequency per week\].
Interventions
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.
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.
Eligibility Criteria
You may qualify if:
- 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
You may not qualify if:
- 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.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Tehsil Headquarter Hospital, Bahlwal
Sargodha, Punjab Province, 40100, Pakistan
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
June 9, 2026
First Posted
June 12, 2026
Study Start
November 2, 2025
Primary Completion
April 29, 2026
Study Completion
May 5, 2026
Last Updated
June 12, 2026
Record last verified: 2026-06
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF, CSR
- Time Frame
- It will be available after the completion of the study.
- Access Criteria
- Data requests should be sent to the corresponding author. Access will be granted to qualified researchers for approved research proposals. Data will be de-identified before sharing.
Only IPD used in the results publication willbe shared.