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Effect of Specific Versus General Hamstring Stretch on Clinical Outcomes in Patellofemoral Pain Syndrome (PFPS)

Not Applicable
Not yet recruiting
Conditions
Hamstring Shortness
Patellofemoral Pain Syndrome
Hamstring Flexibility
Patellofemoral Pain (PFPS)
Registration Number
NCT07013617
Lead Sponsor
Cairo University
Brief Summary

This randomized, Single-blind, parallel-group trial will compare the effects of three hamstring stretching interventions-general hamstring Muscle Energy Technique (MET), medial hamstring MET, and lateral hamstring MET-each combined with standardized TENS and progressive hip/knee strengthening, on hamstring flexibility (knee-extension ROM), anterior knee pain (Arabic Kujala score), pain intensity visual analogue scale (VAS), and lower-limb strength (hand-held dynamometer) in adults with patellofemoral pain syndrome (PFPS).

Detailed Description

Patients with chronic PFPS will be randomized (1:1:1) into:

General MET group: standard non-specific hamstring MET stretch

Medial MET group: targeted medial-hamstring MET stretch

Lateral MET group: targeted lateral-hamstring MET stretch

All groups receive:

TENS: 20 min asymmetric biphasic square-pulse, 120 μs pulse width, 180 Hz, electrodes around patella (5-7 cm apart)

Strengthening: 3×/week for 4 weeks; hip/knee exercises, start 3×10 reps → 3×20, progress with weights or resistance bands.

Outcomes are measured pre-intervention and at 4 weeks. Analysis by mixed-design MANOVA (α \< 0.05).

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Anterior or retropatellar knee pain lasting at least three months
  • Pain reproduced by at least two functional tasks: squatting, kneeling, prolonged sitting, stair climbing, hopping or running
  • Pain intensity of ≥3 on a Visual Analog Scale
  • positive active knee extension test (inability to achieve greater than 160° of knee extension with the hip at 90° of flexion)
  • Body mass index (BMI) < 30 Kg/m² and > 18Kg/m²
Exclusion Criteria
  • Previous knee surgery
  • History of knee pathologies, such as meniscal injury' ligament injury, or knee osteoarthritis
  • Psychological, cardiovascular' or neurological disorders
  • Dizziness or fainting while doing exercises, pregnancy, or any contraindications to exercise
  • Physical therapy treatment in the last 3 months

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
hamstring flexibility (knee extension range of motion )4 weeks

measuring knee extension range of motion(hamstring flexibility) by active knee extension test using kinovea software

Arabic Kujala Anterior knee pain score4 weeks

Arabic Kujala Anterior knee pain score is used to measure pain and functional activities in anterior knee pain patients consisting of 13 questions, the Patient will be asked to mark the most suitable answer for him. Each answer has points up to 5 or 10, and the total score is 100.

The higher the score, the better for the patient.

Secondary Outcome Measures
NameTimeMethod
pain intensity by visual analogue scale (VAS)4 weeks

from 0 to 10 centimeter line patient will detect on it the usual pain felt and the worst pain during the day

lower limb strength using handheld dynamometer4 weeks

using handheld dynamometer to assessment the strength of hip abductor, extensors, external rotators and knee extensors

Trial Locations

Locations (1)

faculty of physical therapy Cairo university

🇪🇬

Giza, Egypt

faculty of physical therapy Cairo university
🇪🇬Giza, Egypt
Amna Ibrahim Shemila, BSc
Principal Investigator
Ahmed Omar Abdelnaeem, lecturer
Contact
2011407368020
ahmed.omar@pt.cu.edu.eg

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