Neuromuscular Inhibition Technique on Iliotibial Band Friction Syndrome
NCT ID: NCT06980324
Last Updated: 2025-05-20
Study Results
Results pending
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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Recruitment Status
ACTIVE_NOT_RECRUITING
Clinical Phase
NA
Total Enrollment
40 participants
Study Classification
INTERVENTIONAL
Study Start Date
2024-03-02
Study Completion Date
2025-07-31
Brief Summary
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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
* 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
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Detailed Description
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Conditions
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Iliotibial Band Syndrome
Study Design
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Allocation Method
RANDOMIZED
Intervention Model
PARALLEL
Primary Study Purpose
TREATMENT
Blinding Strategy
QUADRUPLE
Participants
Caregivers
Investigators
Outcome Assessors
Study Groups
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control group
Group Type
EXPERIMENTAL
conventional physical therapy treatment
Intervention Type
OTHER
Conventional physical therapy treatment:
* Ultrasound
* Hotpacks
* Iliotibial band stretching
* Static quadriceps and hamstring exercises
Interventional group
Group Type
EXPERIMENTAL
integrated neuromuscular inhibition technique
Intervention Type
OTHER
integrated neuromuscular inhibition technique consists of:
* ischemic compression
* Positional release
* Muscle energy technique
Interventions
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integrated neuromuscular inhibition technique
integrated neuromuscular inhibition technique consists of:
* ischemic compression
* Positional release
* Muscle energy technique
Intervention Type
OTHER
conventional physical therapy treatment
Conventional physical therapy treatment:
* Ultrasound
* Hotpacks
* Iliotibial band stretching
* Static quadriceps and hamstring exercises
Intervention Type
OTHER
Eligibility Criteria
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Inclusion Criteria
* 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
* 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
Exclusion Criteria
* 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
* Pregnancy
* Auto immune disease
* Chronic disease (Diabetes mellitus and Hypertension)
* 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
* Pregnancy
* Auto immune disease
* Chronic disease (Diabetes mellitus and Hypertension)
Minimum Eligible Age
30 Years
Maximum Eligible Age
50 Years
Eligible Sex
ALL
Accepts Healthy Volunteers
No
Sponsors
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Cairo University
OTHER
Sponsor Role
lead
Responsible Party
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Esraa Tarek Farouk
Basic science physical therapist
Responsibility Role
PRINCIPAL_INVESTIGATOR
Principal Investigators
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AMIR MO Saleh, Professor of Physical Therapy
Role: STUDY_CHAIR
Cairo University
Doaa RA Elazab, Assistant professor
Role: STUDY_DIRECTOR
Cairo University
Hassan HU Ahmed, Orthopedic Surgery Professor
Role: STUDY_DIRECTOR
Faculty of Medicine Banha University
Esraa TA Farouk, Physical therapist
Role: PRINCIPAL_INVESTIGATOR
Cairo University
Locations
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Faculty of physical therapy, Cairo university
Giza, , Egypt
Site Status
Countries
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Egypt
References
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Other Identifiers
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P.T.REC/012/004885
Identifier Type: -
Identifier Source: org_study_id
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