Relationship Between Knee Pain And Proprioception During Single Leg Squat In Patellofemoral Pain Syndrome

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-35
SponsorCairo University

About this trial

This study will be conducted to investigate the relationship between knee joint pain intensity and joint position sense accuracy in patients with patellofemoral pain syndrome (PFPS) in a single-leg squat position.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ranges from 18-35 years

BMI ranges from 18-25 kg/m2

Positive eccentric step test

Anterior or retropatellar knee pain present during at least two of the following - ascending/descending stairs, hopping/running, squatting, kneeling and prolonged sitting

Disqualifiers

Knee pain is more than 6 score on ANPRS.

History of traumatic patellar dislocation or subluxation

Osteoarthritis in the knee, ankle or hip joints, injury of cruciate ligaments or menisci

Previous orthopedic disorders or neurologic deficit of the lower limbs, any sensory problems, leg length discrepancy, neuromuscular disease like multiple sclerosis

Trial population

eighty two patellofemoral pain syndrome had Positive eccentric step test,Anterior or retropatellar knee pain present during at least two of the following - ascending/descending stairs, hopping/running, squatting, kneeling and prolonged sitting and Pain on palpation of patellar facets. their ages between 18-35 years old.

Trial design

Design model

Other

Time perspective

Cross-sectional

Treatments tested in this trial

  • patellofemoral pain syndrome patients

    Other intervention

    eighty two patellofemoral pain syndrome had Positive eccentric step test,Anterior or retropatellar knee pain present during at least two of the following - ascending/descending stairs, hopping/running, squatting, kneeling and prolonged sitting and Pain on palpation of patellar facets. their ages between 18-35 years old.

Treatment groups

82 Participants
are divided into 1 treatment group
Group A: patellofemoral pain syndrome patients1 intervention

Trial outcomes

Primary outcomes

1

pain intensity

nemerial pain rating scale will be used to assess pain intensity. It comprises of 11 point ''horizontal scale'' of 0-10 in Arabic numerals anchored by the two ends, the left (0 indicating no pain at all) and right (10 indicating the worst ).

Time frame
up to one day
2

knee disability

The Arabic version of the Kujala patellofemoral pain scoring system is a questionnaire to assess the patient with PFP. It includes 13 points based on the following factors: presence of a limp, need for support, walking ability, stair climbing, squatting, running, jumping, prolonged sitting with knees flexed, pain, swelling, abnormal painful kneecap movement, atrophy of the thigh, and flexion deficiency. Each question has multiple answers with points reflecting the severity of symptoms and level of functional limitation. Each question is assigned a score of either up to 5 or 10, and the total score for the Kujala questionnaire is 100. The higher the score, the better the function

Time frame
up to one day
3

knee joint position error (knee joint proprioception)

Digital-goniometer will be used to assess joint position error.the digital-goniometer will be attached to the knee joint in the neutral knee position. The fixed arm will be placed in parallel to an imaginary line between the head of the fibula and the lateral malleolus. The movable arm will be placed in parallel to an imaginary line between the greater trochanter and the lateral condyle of the femur. The digital-goniometer will be zeroed when the subject is standing motionless in the anatomic position. To prevent slippage during knee joint motion, the end blocks will be adhered to the tested leg with double-sided adhesive tape and further secured in place with adhesive tape. Digital-goniometer readings records knee joint angular displacements relative to zero

Time frame
up to one day

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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