High-Intensity Laser Acupuncture for Treating Patellofemoral Pain Syndrome
1 other identifier
interventional
60
0 countries
N/A
Brief Summary
Patellofemoral pain syndrome (PFPS) is among the most prevalent forms of knee discomfort. The main complaint is typically anterior knee pain, which gets worse while jumping, bending knee, going up or down stairs, or sitting for long periods of time with bent knee. Teens and early adulthood are commonly affected by patellofemoral pain syndrome, with a higher frequency in females. In healthy general populations, the prevalence of patellofemoral pain syndrome is 22.7%, and in teens, it is 28.9%.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Jun 2026
Shorter than P25 for not_applicable
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 12, 2026
CompletedFirst Posted
Study publicly available on registry
June 17, 2026
CompletedStudy Start
First participant enrolled
June 20, 2026
ExpectedPrimary Completion
Last participant's last visit for primary outcome
August 31, 2026
Study Completion
Last participant's last visit for all outcomes
August 31, 2026
June 17, 2026
June 1, 2026
2 months
June 12, 2026
June 12, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Pain Intensity
The visual analogue scale represents the pain range that a patient thinks they might experience. The line is typically 10 centimetres long, with or without markings at each centimetre serves as a representation of the range. The worst pain the patient could possibly envision is represented by one end, while; no pain; is represented by the other. The patient marks the scale by drawing a line on it to indicate the amount of discomfort they are experiencing from 0-10. Higher scores represent worse pain.
4 weeks
Secondary Outcomes (2)
Function of knee joint
4 weeks
patient Satisfaction
4 weeks
Study Arms (2)
high-intensity laser acupuncture and exercise therapy program.
EXPERIMENTALThe patients will receive high-intensity laser acupuncture and exercise therapy program.three times a week for four weeks.
sham laser acupuncture and exercise therapy program.
SHAM COMPARATORThe patients will receive sham acupuncture laser and exercise therapy program three times a week for four weeks.
Interventions
The experimental group will receive high-intensity lasers and the treatment will be applied at over six points (ST34, ST 35, GB34, EX-LE4, SP9, and SP10) Exercise therapy program consisted of stretching for hamstring, gastrocnemius and iliotibial band, and strengthening exercises, which include isometric quadriceps exercises, straight leg raising, lateral straight leg raise, isometric hip adduction and squat to 30° knee flexion, 3 times /week for 4 weeks
Sham laser acupuncture and exercise therapy Program. Exercise therapy program consisted of stretching for hamstring, gastrocnemius and iliotibial band, and strengthening exercises, which include isometric quadriceps exercises, straight leg raising, lateral straight leg raise, isometric hip adduction and squat to 30° knee flexion, 3 times /week for 4 weeks
Eligibility Criteria
You may qualify if:
- Patients with patellofemoral pain syndrome (positive Clarkes sign and Waldron test)
- Age from 18 to 25 years
- Patients suffering from pain which aggravated by prolonged sitting, stair climbing, running, squatting, kneeling, hopping\\jumping, overuse activities and relieved by rest for at least 3 months
- Visual analog scale (VAS) greater than 3 points in daily activity
- The ability to participate in the study and follow the treatment schedule.
You may not qualify if:
- Physiotherapy in the last 12 months
- Intra-articular injection in the last 3 months
- Other knee disorders such as: (osteoarthritis, previous knee surgery, history of knee arthroplasty, or traumatic injury related joint deformity)
- BMI greater than or equal 30
- Pregnancy
- Pacemaker insertion
- Photosensitivity
- History of using oral analgesic or NSAIDs in the previous 4 weeks,
- History of malignancy, psychiatric disorder, mental retardation, neurologic dysfunction, diabetes mellitus, or uncontrolled hypertension.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Masking Details
- random generator
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Lecturer of physical therapy for basic science department., faculty of physical Therapy
Study Record Dates
First Submitted
June 12, 2026
First Posted
June 17, 2026
Study Start (Estimated)
June 20, 2026
Primary Completion (Estimated)
August 31, 2026
Study Completion (Estimated)
August 31, 2026
Last Updated
June 17, 2026
Record last verified: 2026-06