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Comparative Effects Of Clamshell And Short Arc Quadriceps Exercises In Patellofemoral Pain

Comparative Effects Of Clam Shell Exercises And Short Arc Quadriceps Strengthening Exercises On Pain, Functional Disability And Quality Of Life In Patellofemoral Pain Syndrome

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07646431
Acronym
CASCAPE-PFPS
Enrollment
34
Registered
2026-06-12
Start date
2025-11-02
Completion date
2026-05-05
Last updated
2026-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Patellofemoral Pain Syndrome

Keywords

Patellofemoral Pain Syndrome, Clamshell Exercises, Short Arc Quadriceps, Knee Pain, Hip Strengthening, Quadriceps Strengthening, Physical Therapy

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.

Detailed description

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.

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.

PROCEDUREShort Arc Quadriceps Exercise

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.

Sponsors

Green International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)

Intervention model description

Randomized parallel-group study. Patients with patellofemoral pain syndrome will be assigned to Group 1: Clamshell exercise or Group 2: Short arc quadriceps exercise. Both groups receive supervised exercise for same duration.

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frameDescription
Change in Pain IntensityBaseline and 12 weeks post-interventionPain 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.

Secondary

MeasureTime frameDescription
Change in Knee FunctionBaseline and 12 weeks post-interventionKnee 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.
Change in Quality of LifeBaseline and 12 weeks post-interventionQuality 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.

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 13, 2026