Recruiting NCT06803914
Analysis of Biomechanical Parameters and Return to Sport After Total Hip Replacement
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Biomechanical analysis.
- Who it may be relevant to
- Registry conditions: Hip Arthroplasty, Total. Basic parameters: 18 years — 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- France
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
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Overview
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.
Interventions
- Procedure 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.
Primary outcome measures
- Angular measurements by biomechanical sensors [Time frame: 6 months after surgery]
- Vertical forces measured by biomechanical sensors [Time frame: 6 months after surgery]
Eligibility criteria
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
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
France · 1 center
- Clinique du Sport — Mérignac
Identifiers
NCT: NCT06803914 · 2024-31-SBM