Clinical Trials Logo

Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT06306664
Other study ID # PT.REC/012/004881
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date January 1, 2024
Est. completion date December 1, 2025

Study information

Verified date March 2024
Source Cairo University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purposes of this study are: 1. To examine the combined effects of Yellow CPPNLT and conventional treatment on pain intensity, pain pressure threshold, functional disability, and muscle strength in athletic jumper knee. 2. To examine the combined effects of Green CPPNLT and conventional treatment on pain intensity, pain pressure threshold, functional disability, and muscle strength in athletic jumper knee. 3 3- To compare between the effects of Yellow CPPNLT and Green CPPNLT on pain intensity, pain pressure threshold, functional disability, and muscle strength in athletic jumper knee.


Description:

Jumper's knee is an overuse injury of the tendon that alters the knee due to repeated stress of activities. Symptoms include pain in the front of the knee. The tears are typically caused by accumulated stress on the patellar or quadriceps tendon. As the name implies, the condition is common in athletes from jumping sports, where there is a high demand for the speed and power of leg extensors. These sports often lead to high eccentric quadriceps loadings, such as volleyball, track (long and high jump), basketball, long-distance running, and skiing. The prevalence of jumper knee is not well examined so far. For non-elite adult athletes the prevalence varies between 14.4% and 2.5% for different sports.Only 2.4% of adolescent professional soccer players sustain PT. However, knee pain, focal tenderness or even acute episodes of PT have a major impact on each player's development, time off the pitch, and career.Bioptron was used for treatment of arthritis, neck&back pain by stimulating blood circulation, reducing inflammation and relieving muscle spasm. There are some studies that have discussed the extent of the effect of the Bioptron Light Therapy on musculoskeletal disorders such as; rotator cuff tendinitis, tennis elbow, carpal tunnel syndrome, acute patellar tendinopathy and acute ankle sprain. There is a lack of the evidence of the clinical guidelines of patellar tendinitis. Up to our knowledge, there is no clear recommendation about efficiency of different colors of Bioptron light therapy on jumper knee. So; this study will be conducted to determine efficiency of yellow and green colors of polychromatic non-coherent light. Sixty subjects will participate in this study and will be divided randomly into three equal groups.Group A (Study group): Will receive green filter of bioptron light therapy and conventional treatment for jumper knee,group B (Study group): Will receive yellow filter of bioptron light therapy and conventional treatment for jumper knee and group C (Control group): Will receive conventional treatment (ice application+ exercise program) for jumper knee.


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 60
Est. completion date December 1, 2025
Est. primary completion date November 29, 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 15 Years to 35 Years
Eligibility Inclusion Criteria: - History of Patellar tendinitis and anterior knee pain. - Age will be ranged from 15 to 35 years. - Both genders. - The onset of pain for over 3 months. Exclusion Criteria: - Knee surgery within the previous 6 months. - Chronic joint diseases. - Corticosteroid injection in the patellar tendon within the previous 3 months. - Use of drugs 48 hours previously (e.g., NSAIDs). - Any other concomitant treatment for PT.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Bioptron
Bioptron safely treats arthritis, neck & back pain by stimulating blood circulation, reducing inflammation and relieving muscle spasms. For just ten minutes per day, our life-transforming technology offers the highest levels of pain relief by reaching deep into joints, muscles and ligaments.
Other:
Placebo Comparator
Patients will receive ice application+Exercises program designed for jumper knee

Locations

Country Name City State
Egypt Physical Therapy Giza Dokki

Sponsors (1)

Lead Sponsor Collaborator
Cairo University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Other Muscle strength and endurance ( Biodex-Isokinetic Dynamometer) The subjects will be positioned in sitting on isokinetic chair and we will ask the subjects to perform maximal knee extension and we will record the change of muscle power or endurance The Isokinetic dynamometer will be investigated at baseline and after the treatment period of 4 weeks.
Primary Pain (Visual analogue scale). The visual analog scale (VAS) is a validated, subjective measure for acute and chronic pain. The VAS score for grading of pain consists of a 10 centimeters (cm) line with 10 mm (0.01 cm) to each point of the scale and two end-points representing no pain and worst possible pain. Visual analogue scale will be investigated at baseline and after the treatment period of 4 weeks.
Primary pain intensity (Pressure algometry) Pressure pain threshold will be measured with algometry test FPX25 using 1-cm2 rubber tip on the knee extensors.10, 11 pressures will be applied slowly until the participant first feels the pain and response by saying stop there. Pressure algometry will be investigated at baseline and after the treatment period of 4 weeks.
Primary Disability questionnaire (Victorian institute of sport assessment-patella). The VISA-P, formerly known as the Victorian institute of sport assessment -patella Questionnaire, The VISA-P is questionnaire that assesses symptoms, simple tests of function, and the ability to play sports. The VISA-P questionnaire will be investigated at baseline and after the treatment period of 4 weeks.
Primary Muscle strength (Hand held dynamometer) The subjects will be positioned in sitting on chair and we will apply resistance when performing the dynamometer on patients and they will try to make maximal effort against resistance and we will record the change of length or resistance. The Lafayette hand held dynamometer will be investigated at baseline and after the treatment period of 4 weeks.
See also
  Status Clinical Trial Phase
Completed NCT03096067 - Patellar Tendinopathy - The Effect of Load Magnitude in Exercise-based Treatment N/A
Recruiting NCT05731037 - Influence of Restitution Time in Treatment of Patellar Tendinopathy N/A
Completed NCT03694730 - Continued Activity During Rehabilitation in Patients With Patellar Tendinopathy N/A
Completed NCT01460004 - The Effect of Infrapatellar Strap Treatment on Pain Extent and Athletic Measures in Young Athletes N/A
Completed NCT03917849 - Efficacy of Inertial Flywheel vs Heavy Slow Resistance Training Among Athletes With Patellar Tendinopathy N/A
Recruiting NCT06217432 - A Study of the Effect of Time-of-day of Training on Chronic Patellar Tendinopathy N/A
Active, not recruiting NCT04550013 - Blood Flow Restriction Training for Treatment of Chronic Patellar Tendinopathy N/A