Biomechanical analysis: Biomechanical assessment is performed using a set of sensors (Qualisys Sports Marker Set - functional assessment, already in use at the Clinique du Sport) as well as 3D optoelectronic cameras and force and pressure platforms. These sensors are placed at various points on both lower limbs (hip, knee, ankle) and provide data in different planes (sagittal, frontal, transverse), as well as a comparison of both sides.
Study summary
This prospective study aims to evaluate the dynamic biomechanical parameters of gait in active patients who have undergone total hip replacement (THR), focusing on movements critical for return to sport.
Eligibility
Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria:
* Patient scheduled for total hip replacement surgery
* Active patient with low to high level of physical activity prior to surgery
* Informed consent
* Complete medical file
Exclusion Criteria:
* Contralateral hip surgery
* Neurological disorder affecting movement (e.g. Parkinson's disease, stroke)
* Spinal pathology affecting movement or posture
* Dementia or inability to complete questionnaires and assessments
* Pregnant or breast-feeding patient
* Patient under protective supervision
* Patient not covered by a social security scheme
Primary outcome measure(s)
Angular measurements by biomechanical sensors — 6 months after surgery Angle measurements at hip, pelvis, knee and ankle in the three planes of space (sagittal, frontal and transverse), measured by biomechanical sensors.
Vertical forces measured by biomechanical sensors — 6 months after surgery Vertical forces, push and landing, will be evaluated for each phase of the movements. Biomechanical specific sensors will be used to measure these data
Trial sites (1)
Facility
City
Region
Status
Clinique du Sport
Mérignac
France
Recruiting
More Clinique du Sport, Bordeaux Mérignac trials in France
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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