Skip to content

Ilium Mobilization in Patellofemoral Pain Syndrome Treatment

Efficacy of Adding Posterior Ilium Mobilization With Movement to Treatment of Patellofemoral Pain Syndrome

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05708495
Enrollment
36
Registered
2023-02-01
Start date
2023-06-01
Completion date
2024-05-01
Last updated
2025-05-30

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

Conditions

Patellofemoral Pain Syndrome

Keywords

patellofemoral pain syndrome, strength, stretch, mobilization, ilium, innominate

Brief summary

Aim of the study is to investigate the effect of adding posterior ilium mobilization on knee pain, knee function, anterior pelvic tilt, dynamic knee valgus, muscle strength of extensors, abductors and external rotators of hip and knee extensors in patients with patellofemoral pain syndrome.

Interventions

OTHERposterior ilium mobilization

the therapist will mobilize the innominate on the affected side posteriorly

the participants will receive strengthening exercises on the hip and knee joint beside that they will receive stretching exercises

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

1. Age of the subjects between 18-35 years. 2. BMI will be ≤ 29.5 3. Anterior or retro patellar knee pain for at least 6 weeks duration. 4. Foot posture index score from +6 to +12. 5. Anterior pelvic tilt angle more than 8 degree. 6. Pain elicited at least by two of the following four tests; (i) Isometric muscle contraction with slight bent knee,(ii) palpation of the patellofemoral joint line, (iii) patellar compression against the femoral bone (iv) active resisted knee extension. 7. Pain intensity more than 3 at ANPS and provoked by at least two of the following activities: running, walking, hopping, squatting, stair negotiation, kneeling, or prolonged sitting.

Exclusion criteria

1. Meniscal or other intraarticular pathologic conditions; cruciate or collateral ligament involvement. 2. A history of traumatic patellar subluxation or dislocation. 3. Previous surgery in the knee, ankle and hip joints. 4. Knee, ankle and hip joints osteoarthritis. 5. Taking non-steroidal anti-inflammatory drugs or corticosteroids within 24 h before the test. 6. History of brain injury or vestibular disorder within the last 6 months. 7. Pregnant female.

Design outcomes

Primary

MeasureTime frameDescription
Changes in painIt will be assessed at baseline and after 4 weeksArabic Numeric pain rating scale will be used to assess pain changes during walking, hopping, squatting, stair negotiation, kneeling, or prolonged sitting. This scale measures pain severity on a scale of 0 to 10 points, with 0 representing no pain and 10 signifying the most severe pain possible.
Changes in knee functional disabilityIt will be assessed at baseline and after 4 weeksThe Arabic version of Anterior knee pain scale will be used to assess the knee functional disability. It is a self-administered, weighted questionnaire that analyzes 13 items, including pain and function, with a maximum score of 100 points and minimum score of 0 points. Higher scores indicate greater lower extremity function. It documents responses to six activities linked with anterior knee pain (walking, running, jumping, climbing stairs, squatting, and sitting for prolonged periods with knee bent).

Secondary

MeasureTime frameDescription
Changes in hip external rotators strengthIt will be assessed at baseline and after 4 weeksHandheld dynamometer will be used to assess changes in muscle strength
Changes in knee extensors strengthIt will be assessed at baseline and after 4 weeksHandheld dynamometer will be used to assess changes in muscle strength
Changes in hip abductors strengthIt will be assessed at baseline and after 4 weeksHandheld dynamometer will be used to assess changes in muscle strength
Changes in pelvic tilt angleIt will be assessed at baseline and after 4 weeksPalpation Meter (PALM) will be used to assess changes in pelvic tilt angle
Changes in dynamic knee valgusIt will be assessed at baseline and after 4 weeksCell phone Camera, tripod device and Kinovea Computer Program (KCP) will be used to assess knee frontal plane projection angle to detect changes in knee valgus during step down test
Changes in hip extensors strengthIt will be assessed at baseline and after 4 weeksHandheld dynamometer will be used to assess changes in muscle strength

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026