"Mulligan Technique vs Phonophoresis With Chitosan for Patellofemoral Pain"

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-35
SponsorAhram Canadian University

About this trial

Patellofemoral pain syndrome (PFPS) is a common knee condition causing pain and dysfunction. This study aims to compare the effectiveness of two physical therapy treatments for PFPS: Mulligan mobilization with movement technique versus phonophoresis with chitosan gel.

Forty-five participants with patellofemoral pain syndrome will be randomly assigned to one of three groups: (1) Mulligan technique group, (2) Phonophoresis with chitosan gel group, or (3) Control group receiving standard physical therapy exercises. Each group will receive treatment 3 times per week for 4 weeks.

The researchers want to determine which treatment is more effective in improving neuromuscular control, reducing pain, and improving function in patients with patellofemoral pain syndrome. Participants will be assessed before and after the treatment period.

This study may help physical therapists and healthcare providers choose the most effective treatment approach for patients with patellofemoral pain.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Insidious onset of anterior knee pain

Retro patellar or peripatellar pain

Pain duration more than four weeks (chronic/subacute)

Pain severity ≥ 3/10 on Visual Analog Scale (VAS)

Disqualifiers

Traumatic injury (e.g., dislocation, fracture, ligament or meniscus pathology)

Inflammatory arthritis (e.g., rheumatoid arthritis, gout)

Prior knee surgery

Current use of NSAIDs or corticosteroids

Trial design

Design model

Parallel

Treatments tested in this trial

  • Mulligan technique

    Procedure/Surgery

    Each mobilization with movement (MWM) is performed in three sets of 10 repetitions, with a 30-second rest interval between sets, 3 times per week for 6 weeks, before hip and knee strengthening exercises.

  • Phonophoresis with Chitosan Gel

    Procedure/Surgery

    Phonophoresis (ultrasound with chitosan gel) is applied at 1 MHz, 1.0 W/cm², continuous mode, for 5 minutes, 3 times per week for 6 weeks before hip and knee exercises.

  • Standard Physical Therapy Exercise Program

    Behavioral

    Participants attend 3 sessions per week for 6 weeks. Each session includes stretching and hip and knee focused exercises. Progression involves weekly increases in repetitions and resistance based on pain levels (less than 3/10).

Treatment groups

45 Participants
are divided into 3 treatment groups
Group A: Mulligan Technique GroupExperimental treatment 1 intervention
Group B: Phonophoresis with Chitosan GroupExperimental treatment 1 intervention
Group C: Control Group ( Standard Physical Therapy Group)Active comparator 1 intervention

Trial outcomes

Primary outcomes

1

Maximal rate of force development (RFD)

Calculated from the slope of force- or torque-time curves obtained during rapid, explosive voluntary contractions also termed ballistic or rapid actions has become a key metric for assessing explosive strength in diverse populations, including athletes, older adults, and clinical patients

Time frame
Baseline and 6 weeks
2

Pain at patella

Pain measured using the Kujala Anterior Knee Pain Scale (AKPS). The scale ranges from 0 to 100 points, with 0 indicating maximum disability and 100 indicating no disability. Higher scores indicate better outcome (less pain and better function)

Time frame
Baseline and 6 weeks

Secondary outcomes

Other outcomes

Locations

1

Map coordinates are unavailable for these locations. Locations are shown below instead.

Ahram Canadian unveracity Status unavailable 12573, Cairo, Giza GovernorateEgyptEgypt

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

This trial is not recruiting at the moment. You can still explore other options: