Clinical Trials Logo

Clinical Trial Summary

The aim of this study is to investigate the effectiveness of high-intensity laser therapy on pain and lower extremity function in the treatment of patellofemoral pain syndrome.


Clinical Trial Description

Participants between the ages of 25-45 who were diagnosed with Unilateral patellofemoral pain syndrome by the doctor will be included in the study. Also positive Clarke's test and patellar compression tests will be determined as inclusion criteria. The 45 participants will be randomly divided into three groups. Both groups will receive 2 weeks (5 sessions per week) of therapy. First group patients underwent High Intensity Laser Therapy (HILT) and exercises. Second group patients will be treated by transcutaneous electrical nerve stimulation(TENS), ultrasound (US) and exercise for 10 sessions. Also In the third group patients will be treated with ultrasound (US),interferential current stimulation and exercise. All groups receive the same exercise exercise protocol including muscle strengthening and flexibility training for 12 weeks. The outcomes will be pain intensity measured by visual analog scale (VAS) , knee flexion range of motion (FROM), timed up and go test (TUG),muscle strength measured with handheld dynamometer, Pressure Pain Threshold with an algometry and functionality of knee measured by the Lower extremity functional scale and Kujala patellofemoral questionnaire. Statistical analyzes will be performed to compare amounts at baseline, immediately after treatment, and after 12 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05075525
Study type Interventional
Source Istanbul Medipol University Hospital
Contact
Status Active, not recruiting
Phase N/A
Start date September 10, 2021
Completion date June 10, 2022

See also
  Status Clinical Trial Phase
Recruiting NCT05864833 - METabolism After Orthopedic Surgery
Completed NCT03286543 - Electrical Stimulation for the Treatment of Pain Following Total Knee Arthroplasty Using the SPRINT Beta System N/A
Recruiting NCT05461326 - Quadriceps Tendon Versus Bone Patellar Tendon Bone Autograft ACL Reconstruction RCT N/A
Completed NCT06080685 - Efficacy of Character Strengths Intervention in Enhancing Character Strengths and Self-esteem Among Adolescents N/A
Not yet recruiting NCT06002009 - SupraScapular Cuff Study: Assessing the Effects of Size and Type of Rotator Cuff Tear on Suprascapular Nerve Function
Completed NCT04730115 - Evaluation of Architectural Changes in Mandibular Bone Pattern After Functional Treatment by Fractal Dimension Analysis
Withdrawn NCT03436667 - Perioperative Factors Impacting Surgical Risk and Outcomes in Children
Completed NCT03299920 - Opioid Consumption After Knee Arthroscopy N/A
Completed NCT06158165 - Evaluating The Cardiovascular Effects of Tourniquet Application
Recruiting NCT04891549 - Tension Band Versus Locking Plate Fixation for the Treatment of Patella Fractures N/A
Recruiting NCT04676841 - Wound Contamination During Orthopaedic Surgery
Not yet recruiting NCT03899298 - Safety and Clinical Outcomes With Amniotic and Umbilical Cord Tissue Therapy for Numerous Medical Conditions Phase 1
Completed NCT04514601 - A Quality Improvement Project to Assess and Refine the Handover Process at Morning Trauma Meetings
Not yet recruiting NCT04546594 - Epidemiological Data on Pain
Completed NCT05396924 - Rectal Temperature Measurement in Detecting Hypothermia During Hip Arthroscopy N/A
Active, not recruiting NCT05795127 - Risk for Reoperation After First MTP Joint Arthrodesis
Completed NCT04481711 - Total Knee Arthroplasty and Clinical Findings N/A
Completed NCT05928663 - The Effect of Using Double Gloves on Perforation in Orthopedic Surgery N/A
Completed NCT03395171 - Vitamin D3 Supplementation and Stress Fracture Occurrence in High-Risk Collegiate Athletes N/A
Not yet recruiting NCT05603871 - Ligamentoplasty of Ligamentum Tere Developmental Dysplasia of the Hip