Popliteus Muscle Release Versus Patellofemoral Mobilization in Patellofemoral Pain Syndrome

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-30
SponsorCairo University

About this trial

This study will be conducted to compare the effect of popliteus muscle release and patellofemoral mobilization on pain intensity, function, and quadriceps muscle strength in patients with patellofemoral pain syndrome?

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Male and female participants aged 18-30 years.

minimum history of 3 months of unilateral PFP.

pain intensity score of ≥3 on a 10-cm Visual Analog Scale (VAS) for worst pain experienced during the previous week.

Pain reproduced during at least two of the following functional activities: stair ascent or descent, running, hopping, prolonged sitting, squatting, or kneeling.

Disqualifiers

Clinical, x-ray, or MRI findings indicative of other specific pathology including osteoarthritis, meniscal, ligament or cartilage injury, apophysitis.

Recurrent patellar subluxation or dislocation.

Cortisone use over an extended period of time.

Previous surgery to the knee joint; trauma to the knee joint affecting the presenting clinical condition.

Trial design

Design model

Parallel

Treatments tested in this trial

  • Popliteus Muscle Release

    Other intervention

    the participant will lie supine and relaxed on a treatment bench. The therapist will begin the treatment by flexing the participant's knee to approximately 15-25 degrees. Then, the therapist will apply pressure to the popliteus muscle while simultaneously extending the knee to approximately 5 degrees of flexion. When the knee is extended, the pressure will be released. The therapist will repeat this procedure for up to 2 minutes plus tradional therapy

  • Patellofemoral Mobilization

    Other intervention

    Following the clinical guidelines established by Brukner and Khan, the mobilization will be performed with the patient in a supine position to ensure complete relaxation of the quadriceps musculature, thereby minimizing joint compressive forces. The intervention will include multidirectional glides tailored to specific functional deficits:Superior glides,Inferior glides,Medial-lateral excursions and tilt mobilization.Each mobilization will be applied as a gentle sustained glide for duration of 30 to 60 seconds per repetition

  • traditional therapy

    Other intervention

    patients will receive quadriceps muscle strength, hip extension strength, hamstring stretch.

Treatment groups

48 Participants
are divided into 3 treatment groups
Group A: Popliteus Muscle ReleaseExperimental treatment 2 interventions
Group B: Patellofemoral MobilizationExperimental treatment 2 interventions
Group C: traditional therapyActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

pain intensity

The scale used will be the visual analogue scale (VAS), which consists of a line, usually 10 cm long, the patient will be instructed to place a vertical mark on to indicate his/ her pain, ranging from no pain or discomfort (0), to the worst pain that could possibly feel

Time frame
up to four weeks

Secondary outcomes

1

knee disability

The Kujala Arabic version will be used to assess knee disability. it is 13 items on the scale are used to assess subjective symptoms and functional restrictions. A score can have a minimum of 0 points or a maximum of 100 points.Lower scores reflect greater pain and disability

Time frame
up to four weeks
2

quadriceps muscle strength

A handheld dynamometer will be used to assess quadrecips muscle strength

Time frame
up to four weeks

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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