Actively Recruiting

Phase Not Applicable
Age: 20Years - 40Years
All Genders
ID06875804

Effects of Compressive Myofascial Release of the Vastus Lateralis on Lateral Patellar Tracking in Patients With Patellofemoral Pain Syndrome

Led by Riphah International University · Updated on 2025-03-13

24

Participants Needed

1

Research Sites

1 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Patellofemoral Pain Syndrome (PFPS) is a common condition causing pain at the front of the knee, especially during activities like squatting, running, or climbing stairs. It is often linked to improper movement of the kneecap, particularly when it moves too far to the side. This can be influenced by muscle imbalances, especially involving the vastus lateralis muscle. This research investigates how compressive myofascial release (CMFR) therapy on this muscle might improve kneecap movement and reduce symptoms in people with PFPS. The study is a randomized controlled trial involving 26 patients diagnosed with PFPS, aged 20 to 40 years. Participants are divided into two groups: one receiving standard physical therapy focused on pain relief, muscle relaxation, and strengthening, and the other receiving the same therapy plus CMFR on the vastus lateralis muscle. Treatments are given three times per week for four weeks. CMFR involves applying pressure and stretching techniques to reduce muscle tightness and improve function. During the study, participants will have their kneecap movement measured using q-angle analysis before and after treatment. Pain levels and knee function will also be assessed with the Numeric Pain Rating Scale and Kujala Patellofemoral Score. Researchers will track progress and compare results between groups using statistical analysis. The study aims to understand the effects of CMFR on knee mechanics and symptoms over the four-week treatment period.

CONDITIONS

Brief Title

Compressive Myofascial Release of the Vastus Lateralis on Lateral Patellar Tracking in Patellofemoral Pain Syndrome

Who Can Participate

Age: 20Years - 40Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age group between 20 to 40 years
  • Male and female gender
  • Diagnosed cases of Patellofemoral syndrome
  • Participants with positive J sign and Clarke's test
  • Pain provoked during knee loading physical activity, such as jumping, running, squatting, or going up or down stairs in last 3 months
  • Presence of excessive lateral patellar tracking on axial view radiographs
Not Eligible

You will not qualify if you...

  • History of knee surgery in the past year
  • Any contraindications to myofascial release therapy, such as active infections, open wounds
  • Presence of hip pathology or other knee conditions such as ligament tears, meniscal injuries, Osgood-Schlatter or Sinding-Larsen-Johanssen syndrome or jumpers knee
  • Participants with a history of trauma or repetitive episodes of patellar subluxation or dislocation
  • Use of intra-articular corticosteroid injections
  • Presence of auto-immune disorder (spondylolisthesis, spondylitis, Rheumatoid arthritis etc.) other than knee OA or systemic conditions such as severe cardiovascular disease

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 4 weeks

Participants receive baseline physical therapy treatment focusing on pain relief, muscle relaxation, and strengthening. The experimental group also receives compressive myofascial release of the vastus lateralis to address lateral patellar tracking.

Multiple visits during the 4-week treatment period

Trial Site Locations

Total: 1 location

1

Social Security Hospital

Lahore, Punjab Province, Pakistan, 54000

Actively Recruiting

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Research Team

I

Imran Amjad, PHD*

I

Imran Amjad, PHD*

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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Published Research Related To This Trial

The Effect of Self-Myofascial Release on the Pennation Angle of the Vastus Medialis Oblique and the Vastus Lateralis in Athletic Male Individuals: An Ultrasound Investigation.

Queenie Mae Torrente, Alban Killingback, Claire Robertson...

https://pubmed.ncbi.nlm.nih.gov/35693863

Comparison of Compressive Myofascial Release and the Graston Technique for Improving Ankle-Dorsiflexion Range of Motion.

Justin Stanek, Taylor Sullivan, Samantha Davis

https://pubmed.ncbi.nlm.nih.gov/29373060

Osteopathic Manipulative Treatment Versus Exercise Program in Runners With Patellofemoral Pain Syndrome: A Randomized Controlled Trial.

Julio Zago, Fellipe Amatuzzi, Tatiana Rondinel...

https://pubmed.ncbi.nlm.nih.gov/33333491

Ultrasound characteristics of the lateral retinaculum in 10 patients with patellofemoral pain syndrome compared to healthy controls.

Esther J M Schoots, Igor J R Tak, Bertil J Veenstra...

https://pubmed.ncbi.nlm.nih.gov/24139014