Actively Recruiting
The Relationship Between Gait and Severity of Femoroacetabular Impingement
Led by Gazi University · Updated on 2024-08-02
25
Participants Needed
1
Research Sites
156 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
In this study, the spatiotemporal gait parameters of symptomatic femoroacetabular impingement (FAI) patients scheduled for hip arthroscopy are evaluated. Radiological measurements, including the Alpha angle (AA), Lateral Center-Edge Angle (LCEA), and Kellgren-Lawrence (KL) osteoarthritis classification, are recorded from patient files. The relationship between these radiological measurements and walking parameters is assessed. Additionally, the spatiotemporal gait parameters of FAI patients are compared with those of a healthy control group. Walking assessments provide valuable insights into how Femoroacetabular Impingement (FAI) affects movement and aid in evaluating treatment outcomes. Research indicates that individuals with FAI experience reduced hip motion and slower walking speeds. By analyzing spatiotemporal gait parameters-such as gait velocity, cadence, step length, and vertical center of mass-the impact of FAI on walking can be better understood, leading to the development of targeted treatment strategies. The goal is to explore the correlation between these gait parameters and imaging-based FAI characteristics in affected individuals.
CONDITIONS
Official Title
The Relationship Between Gait and Severity of Femoroacetabular Impingement
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients with femoroacetabular impingement scheduled for hip arthroscopy
You will not qualify if you...
- Severe hip osteoarthritis
- Hip dysplasia
- Previous ipsilateral and/or contralateral hip surgery
- Any orthopedic or neurologic pathology that may affect gait patterns
AI-Screening
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Trial Site Locations
Total: 1 location
1
Gazi University Hospital
Ankara, Turkey (Türkiye), 06500
Actively Recruiting
Research Team
İ
İnci H Ayas, Msc
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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