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Clinical Trials in Turkey / NCT07562425
Recruiting Not applicable

Effects of Isometric, Isotonic, and Eccentric VMO Exercises in Patellofemoral Pain Syndrome

NCT07562425 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-08-20
Last updated
2026-08-11

Condition(s) studied

Patellofemoral Pain SyndromeAnterior Knee Pain

Investigational drug(s) / intervention(s)

Isometric VMO ExerciseIsotonic VMO ExerciseEccentric VMO Exercise

Isometric VMO Exercise: Isometric contractions of the vastus medialis oblique muscle will be performed with the knee supported at approximately 15° flexion, emphasizing maximal voluntary contraction without joint movement.

Isotonic VMO Exercise: Participants will perform controlled concentric and eccentric contractions using ankle weights through a limited range of motion (0-30° knee extension).

Eccentric VMO Exercise: Participants will perform eccentric contractions against resistance during knee flexion, with assisted concentric return to the starting position.

Study summary

Patellofemoral pain syndrome (PFPS) is a common musculoskeletal condition characterized by anterior knee pain, especially during activities such as stair climbing, squatting, running, and prolonged sitting. Weakness or delayed activation of the vastus medialis oblique (VMO) muscle is considered an important contributing factor in the development of PFPS.

This study aims to compare the effects of three different types of VMO strengthening exercises (isometric, isotonic, and eccentric) applied within the terminal knee extension range (0-30°) on pain, functional performance, and muscle architecture in individuals with PFPS.

Participants will be randomly assigned to one of three exercise groups. All participants will receive a standardized physiotherapy program, including heat therapy, TENS, and therapeutic ultrasound, followed by group-specific VMO strengthening exercises. The intervention will be performed three times per week for 8 weeks.

Outcomes will be assessed before and after the intervention and will include pain intensity (Visual Analog Scale), functional performance (WOMAC, 30-second sit-to-stand test, and stair test), and muscle architecture parameters measured by ultrasound imaging.

The results of this study are expected to provide evidence for optimizing rehabilitation strategies in individuals with PFPS.

Eligibility

Sex
ALL
Min age
18 Years
Max age
50 Years
Healthy volunteers
No
Inclusion Criteria: * Aged between 18 and 40 years * Clinically diagnosed with patellofemoral pain syndrome * Presence of anterior knee pain for at least 3 months * Pain during activities such as stair climbing, squatting, running, or prolonged sitting * Pain intensity of at least 3/10 on the Visual Analog Scale (VAS) * Willingness to participate and provide written informed consent Exclusion Criteria: * History of knee trauma or surgery * Meniscal injury, ligament injury, or knee instability * Advanced osteoarthritis * Neurological disorders * Rheumatologic diseases * Participation in a structured knee rehabilitation program within the last 6 months * Pregnancy

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Firat University Elâzığ MErkez Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07562425 on ClinicalTrials.gov ↗ ← All trials in Turkey