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Ilium Mobilization in Patellofemoral Pain Syndrome Treatment

Primary Purpose

Patellofemoral Pain Syndrome

Status
Recruiting
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
posterior ilium mobilization
strengthening and stretching exercises
Sponsored by
Cairo University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Patellofemoral Pain Syndrome focused on measuring patellofemoral pain syndrome, strength, stretch, mobilization, ilium, innominate

Eligibility Criteria

18 Years - 35 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age of the subjects between 18-35 years. BMI will be ≤ 29.5 Anterior or retro patellar knee pain for at least 6 weeks duration. Foot posture index score from +6 to +12. Anterior pelvic tilt angle more than 8 degree. 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. 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: Meniscal or other intraarticular pathologic conditions; cruciate or collateral ligament involvement. A history of traumatic patellar subluxation or dislocation. Previous surgery in the knee, ankle and hip joints. Knee, ankle and hip joints osteoarthritis. Taking non-steroidal anti-inflammatory drugs or corticosteroids within 24 h before the test. History of brain injury or vestibular disorder within the last 6 months. Pregnant female.

Sites / Locations

  • Faculty of Physical Therapy, Cairo UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Group 1

Group 2

Arm Description

Outcomes

Primary Outcome Measures

Changes in pain
Arabic Numeric pain scale (ANPS) will be used to assess pain changes during walking, hopping, squatting, stair negotiation, kneeling, or prolonged sitting.
Changes in knee functional disability
The Arabic version of Anterior knee pain scale (AKPS) will be used to assess the knee functional disability

Secondary Outcome Measures

Changes in hip abductors strength
Handheld dynamometer will be used to assess changes in muscle strength
Changes in hip extensors strength
Handheld dynamometer will be used to assess changes in muscle strength
Changes in hip external rotators strength
Handheld dynamometer will be used to assess changes in muscle strength
Changes in knee extensors strength
Handheld dynamometer will be used to assess changes in muscle strength
Changes in dynamic knee valgus
Cell 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 pelvic tilt angle
Palpation Meter (PALM) will be used to assess changes in pelvic tilt angle

Full Information

First Posted
January 23, 2023
Last Updated
January 23, 2023
Sponsor
Cairo University
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1. Study Identification

Unique Protocol Identification Number
NCT05708495
Brief Title
Ilium Mobilization in Patellofemoral Pain Syndrome Treatment
Official Title
Efficacy of Adding Posterior Ilium Mobilization to Treatment of Patellofemoral Pain Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 1, 2023 (Anticipated)
Primary Completion Date
November 1, 2023 (Anticipated)
Study Completion Date
December 1, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cairo University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Patellofemoral Pain Syndrome
Keywords
patellofemoral pain syndrome, strength, stretch, mobilization, ilium, innominate

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
42 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group 1
Arm Type
Active Comparator
Arm Title
Group 2
Arm Type
Experimental
Intervention Type
Other
Intervention Name(s)
posterior ilium mobilization
Intervention Description
the therapist will mobilize the innominate on the affected side posteriorly
Intervention Type
Other
Intervention Name(s)
strengthening and stretching exercises
Intervention Description
the participants will receive strengthening exercises on the hip and knee joint beside that they will receive stretching exercises
Primary Outcome Measure Information:
Title
Changes in pain
Description
Arabic Numeric pain scale (ANPS) will be used to assess pain changes during walking, hopping, squatting, stair negotiation, kneeling, or prolonged sitting.
Time Frame
It will be assessed at baseline and after 4 weeks
Title
Changes in knee functional disability
Description
The Arabic version of Anterior knee pain scale (AKPS) will be used to assess the knee functional disability
Time Frame
It will be assessed at baseline and after 4 weeks
Secondary Outcome Measure Information:
Title
Changes in hip abductors strength
Description
Handheld dynamometer will be used to assess changes in muscle strength
Time Frame
It will be assessed at baseline and after 4 weeks
Title
Changes in hip extensors strength
Description
Handheld dynamometer will be used to assess changes in muscle strength
Time Frame
It will be assessed at baseline and after 4 weeks
Title
Changes in hip external rotators strength
Description
Handheld dynamometer will be used to assess changes in muscle strength
Time Frame
It will be assessed at baseline and after 4 weeks
Title
Changes in knee extensors strength
Description
Handheld dynamometer will be used to assess changes in muscle strength
Time Frame
It will be assessed at baseline and after 4 weeks
Title
Changes in dynamic knee valgus
Description
Cell 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
Time Frame
It will be assessed at baseline and after 4 weeks
Title
Changes in pelvic tilt angle
Description
Palpation Meter (PALM) will be used to assess changes in pelvic tilt angle
Time Frame
It will be assessed at baseline and after 4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age of the subjects between 18-35 years. BMI will be ≤ 29.5 Anterior or retro patellar knee pain for at least 6 weeks duration. Foot posture index score from +6 to +12. Anterior pelvic tilt angle more than 8 degree. 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. 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: Meniscal or other intraarticular pathologic conditions; cruciate or collateral ligament involvement. A history of traumatic patellar subluxation or dislocation. Previous surgery in the knee, ankle and hip joints. Knee, ankle and hip joints osteoarthritis. Taking non-steroidal anti-inflammatory drugs or corticosteroids within 24 h before the test. History of brain injury or vestibular disorder within the last 6 months. Pregnant female.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Labib M Ghali, MSc
Phone
00201201991948
Email
labibmousa7@cu.ed.eg
Facility Information:
Facility Name
Faculty of Physical Therapy, Cairo University
City
Giza
Country
Egypt
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Labib M Ghali, MSc
Phone
00201558052155
Email
labibmousa7@gmail.com
First Name & Middle Initial & Last Name & Degree
Labib M Ghali, MSc

12. IPD Sharing Statement

Learn more about this trial

Ilium Mobilization in Patellofemoral Pain Syndrome Treatment

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