Orthopedic Disorder, Physical Therapy
Conditions
Keywords
Patellofemoral pain, High intensity laser therapy
Brief 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.
Detailed 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.
Interventions
OTHERHigh Intensity Laser Therapy Group
High Intensity Laser Therapy (HILT) and exercises will be used.
OTHERUltrasound and Transcutaneous Electrical Nerve Stimulation Group
Transcutaneous electrical nerve stimulation(TENS), ultrasound (US) will be applied.
OTHERUltrasound and Interferential Current Stimulation Group
Ultrasound (US) ,interferential current stimulation and exercise will be used.
Sponsors
Istanbul Medipol University Hospital
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)
Masking description
Participants are blinded to allocation and outcomes measures.
Eligibility
Sex/Gender
ALL
Age
25 Years to 45 Years
Healthy volunteers
No
Inclusion criteria
* Unilateral patellofemoral pain syndrome diagnosed by a doctor * 25-45 years old * pain from prolonged sitting, climbing and descending stairs, running,knee bend more than 3 months * positive patellar compression and clarke's tests.
Exclusion criteria
* Previous knee pain, trauma, surgery and other joint diseases, * Knee ligament, bursa, meniscus and synovial fold injury or dysfunction * Osteoarthritis in the knee joint, * Neurological problems that may affect walking * Pregnancy * No chronic disease * Malignancy, * Presence of infection
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Muscle stength assesment | 10 minutes | A myometer will be used to measure the strength of the hamstring and quadriceps muscle groups of all participants. Myometer is an evaluation method that objectively evaluates muscle strength and gives more sensitive results than manual muscle testing. |
| Pain threshold assessment | 10 minutes | Pressure pain threshold measurement will be measured with an algometer device. Algometers are a device that can be used to define pressure and pressure pain threshold. |
| Pain status | 5 minutes | Pain intensity was evaluated with visual analog scale (VAS) in two conditions during activity and resting time. This method, which is developed to determine the intensity of pain to indicate by numbers. It begins with the absence of pain (0) on numerical scale and ends the level of unbearable pain |
| Range of motion assesment | 10minutes | Universal goniometer will used to measure the joint position and joint range of motion measurements based on Kendall and American Association of Orthopedic Surgeons. The participant will in the sitting position and asked to perform active cervical region flexion, extension, right and left rotation, right and left lateral flexion of the neck movements and performed degrees will recorded |
| Functionality | 5 minutes | The patients will asked to start from a sitting position in a chair, to get up at the command given, to walk the predetermined distance of 3 meters as fast as they could, and to return to their seats. The time from the time they got up from the chair and sat down again will recorded with a stopwatch. Measurements will be repeated 3 times and the average will be recorded in seconds (sec). |
| Severity and function of patellofemoral pain | 5 minutes | It will be evaluated with the 'Kujala patellofemoral score' system. These scoring system values range from 100 (normal, pain-free, fully functional knee) to 0 (severe knee pain and dysfunction). |
| Function of lower extremity | 10 minutes | A lower extremity function test will be used to measure lower extremity functionality. It is a test used to measure the functional status of the lower extremities. |
Countries
Turkey (Türkiye)
Outcome results
None listed