Comparison Between Foot Segment Mulligan Mobilization and Ilium Mulligan Mobilization in Treatment Patellofemoral Pain Patients With Flatfeet: a Randomized Controlled Comparative Study

NCT ID
NCT07806929
Registry status
Not yet recruiting
Study type
Interventional
Phase
Not applicable
Sponsor
Cairo University
Conditions
Flatfeet, Patellofemoral Pain, PFP

Overview

ClinicalTrials.gov lists this study as Not yet recruiting.

Official title: Targeting the Lower-Limb Kinetic Chain in Patellofemoral Pain: A Randomized Comparison of Foot and Ilium Mulligan Mobilization Combined With Hip-Knee Focused Exercises

Enrollment: 90 participants (Estimated).

What is being studied

  • Other: Hip-knee focused exercises
  • Other: mobilization with movement of the foot segment
  • Other: Mobilization with movement of the Ilium

Who may be eligible

Ages
18 Years to 35 Years
Sex
All
Healthy volunteers accepted
No

ClinicalTrials.gov lists the following eligibility criteria.

Inclusion Criteria: 1. Age of the subjects between 18-35 years 2. BMI was from 18.5 to ≤ 29.5 Kg/m² . 3. Anterior or retro patellar knee pain for at least 6 weeks duration. 4. Foot posture index score from +6 to + 12. 5. Sagittal plane innominate tilt angle more than 8 degrees. 6. Pain elicited at least by two of the following four screening tests; (i) isometric muscle contraction with slight bent knee,(ii) palpation of the patella, (iii) patellar compression against the femoral bone (iv) active resisted knee extension. 7. Pain 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 intra-articular 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 hours before the test. 6. History of brain injury or vestibular disorder within the last 6 months. 7. Pregnant female.

Study locations

1 study location is listed.

Site recruitment status is not specified in the registry data for these locations.

Countries: Jordan

Sample of listed locations

  • Al-Zaytoonah University of Jordan — Amman, 11733, Jordan — Site recruitment status not specified in the registry data

Study details

Start date
October 1, 2026
Primary completion date
November 1, 2027
Completion date
December 1, 2027
First posted
September 8, 2026
Collaborators
Al-Zaytoonah University of Jordan

Source and update information

Source
ClinicalTrials.gov
NCT ID
NCT07806929
Registry last updated
September 8, 2026
QualifiedStudies registry data refreshed
October 5, 2026
QualifiedStudies record fetched
October 5, 2026

View NCT07806929 on ClinicalTrials.gov

Trial information can change. Confirm current study details with the study team or the registry.

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