Neuromuscular Inhibition Technique on Iliotibial Band Friction Syndrome
Effect of Integrated Neuromuscular Inhibition Technique on Iliotibial Band Friction Syndrome
1 other identifier
interventional
40
1 country
1
Brief Summary
The goal of this clinical trial is to find the effect of integrated neuromuscular inhibition technique for iliotibial band in iliotibial band friction syndrome on pain intensity level, pressure pain threshold, knee range of motion, knee function and knee angle . The main questions it aims to answer are:
- Is there an effect of integrated neuromuscular inhibition technique for iliotibial band on pain intensity level in iliotibial band friction syndrome?
- Is there an effect of integrated neuromuscular inhibition technique for iliotibial band on pressure pain threshold in iliotibial band friction syndrome?
- Is there an effect of integrated neuromuscular inhibition technique for iliotibial band on knee range of motion in iliotibial band friction syndrome?
- Is there an effect of integrated neuromuscular inhibition technique for iliotibial band on knee function in iliotibial friction syndrome? Is there an effect of integrated neuromuscular inhibition technique for iliotibial band on knee angle in iliotibial band friction syndrome? Researchers will compare integrated neuromuscular inhibition technique to conventional physiotherapy to see if integrated neuromuscular inhibition technique works to treat iliotibial band syndrome. Participants will:
- Take sessions for 2 weeks
- Visit the department 3 times per week
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 Mar 2024
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 2, 2024
CompletedFirst Submitted
Initial submission to the registry
March 23, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2025
CompletedFirst Posted
Study publicly available on registry
May 20, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2025
CompletedMay 20, 2025
October 1, 2024
1.2 years
March 23, 2025
May 17, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
Pain intensity
The Visual Analogue Scale (VAS) was used to evaluate pain severity. It is a self-reported pain measurement scale, consisting of a horizontal or vertical line, usually 10 cm long. The extremes of the line are labeled as no pain and worst pain. Each subject was asked to mark the point on the line that exactly corresponded to his/her pain
after 2 weeks
lower extremity function
Lower extremity functional scale (LEFS): LEFS is a questionnaire containing 20 items assessing the lower extremity function based on the intensity of the related activities' performance. This scoring system is designed based on the five-score Likert scale ranging from zero as the worst condition to four as without bothersome. This scale scores from zero to eighty and the higher score represent a better condition. LEFS-Arabic version will be used to quantify activity limitation in Arabic-speaking individuals with lower extremity musculoskeletal disorders
after 2 weeks
Knee range of motion
Digital goniometer: A goniometer is a device that measures an angle or permits the rotation of an object to a definite position .To measure knee joint ROM goniometer was lined up with the lateral side of femur with the proximal arm between trochanter major and the middle of the lateral joint space of the knee and the distal arm between the middle of the lateral joint space of the knee and the lateral malleoli
after 2 weeks
Secondary Outcomes (2)
pressure pain threshold
after 2 weeks
knee angle
after 2 weeks
Study Arms (2)
control group
EXPERIMENTALInterventional group
EXPERIMENTALInterventions
integrated neuromuscular inhibition technique consists of: * ischemic compression * Positional release * Muscle energy technique
Conventional physical therapy treatment: * Ultrasound * Hotpacks * Iliotibial band stretching * Static quadriceps and hamstring exercises
Eligibility Criteria
You may qualify if:
- Body mass index from 25-30 kg/m2
- Both males and females will be included their age from 30-50.
- The subjects that will be included in the study will be referred from orthopeadic physician with iliotibial band friction syndrome with these signs and symptoms
- local tenderness of the lateral knee inferior to the epicondyle and superior to the joint line
- Pain with ITBS can be reported anywhere along the iliotibial (IT) band from the lateral thigh to the lateral femoral condyle and Gerdy's tubercle.
- Pain is most intense at approximately 30 degrees of knee.
- A sharp, burning pain when the practitioner presses on the lateral epicondyle during knee flexion and extension associated with one of these cases:
- Tibiofermoral knee pain.
- Patellofemoral knee pain.
- osteoarthritis with medial knee joint pain
- Lateral patellar pressure syndrome.
- Medial meniscus degeneration.
- Excessive lateral pressure syndrome
You may not qualify if:
- Traumatic injury to the knee joint within 6 months.
- Surgical procedure on the affected knee within the last 12 months.
- Meniscus injury
- knee ligaments injury
- Malignancies, tumors or infections associated with the knee joint.
- Impaired thermal sensation over the knee.
- Subject with psychiatric disorder.
- Peripheral vascular disease.
- Severe joint deformity.
- Current back or ankle pain.
- Rheumatoid arthritis.
- Lower extremity fracture.
- Neurological defecit or movement disorder.
- Athletes.
- Menopause
- +3 more criteria
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Sites (1)
Faculty of physical therapy, Cairo university
Giza, Egypt
Related Publications (38)
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BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
AMIR MO Saleh, Professor of Physical Therapy
Cairo University
- STUDY DIRECTOR
Doaa RA Elazab, Assistant professor
Cairo University
- STUDY DIRECTOR
Hassan HU Ahmed, Orthopedic Surgery Professor
Faculty of Medicine Banha University
- PRINCIPAL INVESTIGATOR
Esraa TA Farouk, Physical therapist
Cairo University
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- QUADRUPLE
- Who Masked
- PARTICIPANT, CARE PROVIDER, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Basic science physical therapist
Study Record Dates
First Submitted
March 23, 2025
First Posted
May 20, 2025
Study Start
March 2, 2024
Primary Completion
May 1, 2025
Study Completion
July 1, 2025
Last Updated
May 20, 2025
Record last verified: 2024-10
Data Sharing
- IPD Sharing
- Will not share