Ignite Creation Date:
2024-05-06 @ 6:57 PM
Last Modification Date:
2024-10-26 @ 2:57 PM
Study NCT ID:
NCT05842200
Status:
COMPLETED
Last Update Posted:
2024-01-22
First Post:
2023-04-24
Brief Title:
Influence of Selected Lower Limb Biomechanical Variables on Pain Disability and Balance in Women With PFPS
Sponsor:
Cairo University
Organization:
Cairo University
Study Overview
Official Title:
Influence of Selected Lower Limb Biomechanical Variables on Pain Disability and Balance in Women With Patellofemoral Pain Syndrome A Cross Sectional Study
Status:
COMPLETED
Status Verified Date:
2024-01
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Purpose The aim of this study is to figure out how does the selection of lower-extremity biomechanical variables presented by dynamic knee valgus tibial torsion and navicular drop may influence pain disability and balance in women with patellofemoral pain syndrome
Methods Sixty-five women with patellofemoral pain syndrome will be evaluated for lower limb biomechanical variables
Methods Sixty-five women with patellofemoral pain syndrome will be evaluated for lower limb biomechanical variables
Detailed Description:
Subjects
Sixty five women who will be referred by an Orthopedist with patellofemoral pain syndrome diagnosis
Inclusion criteria
Women were enrolled in this study according to the following criteria
1 Female participants with patellofemoral pain syndrome
2 Age ranges between 18 and 38 years old
3 Bilateral or unilateral involvement
4 Minimum score 3 out of 10-point numerical pain scale NPR
5 Orthopedic clinical confirmation revealing a history of anterior or retro-patellar knee pain aggravated by at least 2 of the following functional activities 1 prolonged sitting 2 stairs use 3 squatting 4 running 5 kneeling 6 hoppingjumping andor insidious onset of symptoms unrelated to any traumatic incident and persistent for at least 6 weeks
Exclusion criteria
A woman was excluded from the study if she has one or more of the following
1 History of patellar dislocation or subluxation
2 Osteoarthritis in the patellofemoral joint
3 Meniscal or other intraarticular pathologic conditions
4 cruciate or collateral ligament involvement
5 Lower limb surgery
6 Fracture low back pain condition such as spondylolisthesis and spondylosis
7 Neurological deficits
8 Traumatic injury or any abnormality in the lower extremity
Methods Sixty-five women with patellofemoral pain syndrome will be evaluated for dynamic knee valgus using Kinovea software program tibial torsion using universal goniometer and navicular drop using calliper
Numerical pain rating scale NPRS will be used to measure pain severity Arabic version of Kujala score will assess the functional disability in these patients
Biodex Balance System will screen and will record the Medial-lateral stability index MLSI Anterior-posterior stability index APSI and an Overall stability index OSI
Assessments will be performed in a single session Then correlation between these variables will be calculated
Sixty five women who will be referred by an Orthopedist with patellofemoral pain syndrome diagnosis
Inclusion criteria
Women were enrolled in this study according to the following criteria
1 Female participants with patellofemoral pain syndrome
2 Age ranges between 18 and 38 years old
3 Bilateral or unilateral involvement
4 Minimum score 3 out of 10-point numerical pain scale NPR
5 Orthopedic clinical confirmation revealing a history of anterior or retro-patellar knee pain aggravated by at least 2 of the following functional activities 1 prolonged sitting 2 stairs use 3 squatting 4 running 5 kneeling 6 hoppingjumping andor insidious onset of symptoms unrelated to any traumatic incident and persistent for at least 6 weeks
Exclusion criteria
A woman was excluded from the study if she has one or more of the following
1 History of patellar dislocation or subluxation
2 Osteoarthritis in the patellofemoral joint
3 Meniscal or other intraarticular pathologic conditions
4 cruciate or collateral ligament involvement
5 Lower limb surgery
6 Fracture low back pain condition such as spondylolisthesis and spondylosis
7 Neurological deficits
8 Traumatic injury or any abnormality in the lower extremity
Methods Sixty-five women with patellofemoral pain syndrome will be evaluated for dynamic knee valgus using Kinovea software program tibial torsion using universal goniometer and navicular drop using calliper
Numerical pain rating scale NPRS will be used to measure pain severity Arabic version of Kujala score will assess the functional disability in these patients
Biodex Balance System will screen and will record the Medial-lateral stability index MLSI Anterior-posterior stability index APSI and an Overall stability index OSI
Assessments will be performed in a single session Then correlation between these variables will be calculated
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None