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A Study on Kinesio Taping for the Precision Prevention and Treatment of Iliotibial Band Syndrome Based on Biomechanics and Clinical Integration

A Study on Kinesio Taping for the Precision Prevention and Treatment of Iliotibial Band Syndrome Based on Biomechanics and Clinical Integration

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500111539
Enrollment
Unknown
Registered
2025-11-02
Start date
2025-11-10
Completion date
Unknown
Last updated
2025-11-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

iliotibial band syndrome

Interventions

Biomechanical Modeling Group (Phase 1):Two patients with ITBS and two running enthusiasts will undergo MRI and CT scans of the hip-thigh-knee segment. Three-dimensional finite element models of the il
tape pre-tension: 10%, 15%, 30%).
ITBS Patient Group (Phase 2):Thirty patients with iliotibial band syndrome (ITBS) each received five kinesio taping interventions in a randomized-order crossover design, including moderate-low tension

Sponsors

Shanghai General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: Phase 1: ITBS Patients: 1. Meeting the diagnostic criteria for iliotibial band friction syndrome (ITBS) (lateral knee pain + positive Ober test + positive Noble compression test); 2. VAS score for lateral knee pain >=4 at rest or during exercise (lasting >=2 weeks); 3. Age 18-55 years old; 4. BMI 18-30 kg/m^2; 5. Forced to reduce exercise volume due to ITBS symptoms in the past month. Running Enthusiasts: 1. Regular exercise habit (running 2-3 times/week for >=6 months, weekly running distance >=30 kilometers, stable pace 5-6 min/km); 2. No history of ITBS (no lateral knee pain, tenderness or functional limitation); 3. Age 18-55 years old; 4. BMI 18-30 kg/m^2. Phase 2: ITBS Patients: 1. Clear exercise history such as running, cycling, etc., and reduced exercise volume due to pain in the past 2 weeks; Clinical manifestations: Unilateral lateral knee pain (VAS >= 4), pain intensifies when knee flexed at 30°; Physical examination: Tenderness at the lateral femoral condyle (+), modified Noble test (+), Ober test (+). 2. Good compliance, voluntarily participating in this study. 3. Age 18-55 years old, BMI 18-30kg/m^2, normal lower limb force line (Q angle < 10° for men, < 15° for women).

Exclusion criteria

Exclusion criteria: Phase 1: ITBS Patients and Running Enthusiasts: 1. Lower limb structural/functional abnormalities (e.g., congenital/ acquired deformities such as genu varum/ valgus, leg length discrepancy >1 cm); 2. Foot malalignment (pes planus or cavus: arch index 0.26); 3. History of other knee injuries (e.g., ligament tear, meniscus injury, chondral lesion); 4. Systemic confounding conditions (e.g., stroke, rheumatoid arthritis, osteoporosis); 5. Presence of metal implants; 6. Claustrophobia or MRI contraindications; 7. Recent interventions (knee surgery or corticosteroid injection within the past 3 months; ITB-specific physical therapy within the past month). Phase 2: ITBS Patients: 1. Poor compliance, unreachable, or unable to complete follow-up; 2. Comorbidities: osteoarthritis, patellofemoral pain syndrome, rheumatoid arthritis, lumbar radiculopathy, sarcoidosis, acromegaly; 3. Cognitive impairment, psychiatric disorders, or current use of psychotropic medications; 4. Recent medication/injections: NSAIDs within 72 hours; knee injections (corticosteroids/PRP) within 4 weeks; 5. Local skin infection or ulceration.

Design outcomes

Primary

MeasureTime frame
Pain intensification distance;Iliotibial Band Stress Suppression Rate;Contact Pressure at the Lateral Femoral Epicondyle;

Secondary

MeasureTime frame
Peak value of hip adduction angle;Delayed activation of the lateral thigh muscle;Iliotibial band thickness;

Countries

China

Contacts

Public ContactFei He

Shanghai General Hospital

hefei111616@163.com+86 135 2405 2516

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026