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NCT Number: NCT07562425

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

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.

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Key information

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Firat University

Elâzığ, MErkez, 23200, Turkey (Türkiye)

Location contact

Muhammet Şahin Elbastı, PhD

PRINCIPAL_INVESTIGATOR

Muharrem Beydağı, PhD

CONTACT

[email protected]

05323581105

About this study

Patellofemoral pain syndrome (PFPS) is a prevalent condition affecting physically active individuals and is associated with anterior knee pain during functional activities. Alterations in patellofemoral joint biomechanics, particularly related to quadriceps muscle imbalance and insufficient activation of the vastus medialis oblique (VMO), are considered key contributing factors.

Although VMO strengthening is widely used in clinical practice, there is limited evidence comparing the effects of different contraction types-specifically isometric, isotonic, and eccentric exercises-applied within the terminal knee extension range (0-30°), where patellofemoral joint stress and stabilization demands are highest.

This study is designed as a three-arm, parallel-group, randomized controlled trial to investigate the comparative effects of these exercise modalities on pain, functional outcomes, and muscle architecture. The intervention period will last 8 weeks, with sessions conducted three times per week.

A total of 90 participants aged 18-40 years with clinically diagnosed PFPS will be recruited and randomly allocated into three groups: isometric, isotonic, and eccentric exercise groups. All participants will receive a standardized physiotherapy protocol including superficial heat application, transcutaneous electrical nerve stimulation (TENS), and therapeutic ultrasound prior to exercise.

Primary outcomes will include pain intensity assessed by the Visual Analog Scale (VAS) and functional status evaluated using the WOMAC index, 30-second sit-to-stand test, and stair ascent/descent test. Secondary outcomes will include ultrasonographic assessment of muscle architecture, including muscle thickness, fascicle length, pennation angle, and physiological cross-sectional area of the VMO muscle. Additionally, selected hip muscles (adductor group and tensor fascia lata) will be evaluated.

Assessments will be performed at baseline (T0) and after the 8-week intervention (T1) by a blinded assessor. Randomization will be conducted using a computer-generated sequence with allocation concealment.

Statistical analyses will include repeated measures analysis to evaluate within-group and between-group differences, with significance set at p < 0.05.

The findings of this study are expected to contribute to evidence-based rehabilitation by identifying the most effective type of VMO strengthening exercise for improving clinical outcomes and muscle structure in individuals with PFPS.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Isometric VMO Exercise

Other

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.

Other names: Experimental: Isometric Exercise Group

Isotonic VMO Exercise

Other

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

Eccentric VMO Exercise

Other

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

Primary outcomes

  1. VMO Muscle Architecture (Ultrasound)

    Time frame: Baseline and Week 8

    Muscle thickness, fascicle length, pennation angle, and physiological cross-sectional area of the vastus medialis oblique muscle will be assessed using ultrasound imaging.

Secondary outcomes

  1. Pain Intensity (Visual Analog Scale, VAS)

    Time frame: Baseline and Week 8

    Pain intensity will be assessed using the Visual Analog Scale (VAS), a 10-cm scale ranging from 0 (no pain) to 10 (worst imaginable pain). Higher scores indicate greater pain intensity.

  2. Functional Status (WOMAC Index)

    Time frame: Baseline and Week 8

    Functional status will be evaluated using the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), including pain, stiffness, and physical function subscales. Higher scores indicate worse functional status.

  3. 30-Second Sit-to-Stand Test

    Time frame: Baseline and Week 8

    The number of repetitions completed in 30 seconds will be recorded to assess lower extremity functional strength.

  4. Stair Ascent and Descent Test

    Time frame: Baseline and Week 8

    Time required to ascend and descend a standardized 9-step staircase will be recorded in seconds.

  5. Hip Muscle Architecture (Ultrasound)

    Time frame: Baseline and Week 8

    Muscle architecture parameters of the hip muscles (adductors and tensor fascia lata) will be evaluated using ultrasound imaging.

Study contacts

Contact information is provided by the study sponsor or research team.

Muharrem Gökhan Beydağı, PhD

CONTACT

[email protected]

+905323581105

Sponsors and collaborators

Lead sponsor

Firat University

Other

Registry information

Official study title

Comparison of the Effects of Isometric, Isotonic, and Eccentric Vastus Medialis Oblique Strengthening Exercises Applied in Terminal Knee Extension Range on Pain, Function, and Muscle Architecture in Individuals With Patellofemoral Pain Syndrome: A Randomized Controlled Trial

Acronym: VMO-PFPS

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
May 1, 2026
Registry last updated
May 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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