The purpose of this study is to describe and compare the kinematic deficiencies specifically associated with each of the 3 main clinical phenotypes of patellofemoral pain syndrome. The prevalence of patellofemoral pain is high with a high rate of chronicity and recurrence and an overrepresentation of young, athletic and female populations. There are multiple classifications of patellofemoral pain syndrome. A pragmatic classification distinguishes 3 main clinical phenotypes of patellofemoral pain syndrome: with objectively displaceable patella, with extra-patellar alignment problems and without alignment problems. The pathophysiology of patellofemoral pain syndrome is multifactorial involving static and dynamic dysfunctions of the hip, knee and foot, which remain incompletely elucidated to date. The links between the clinical and biomechanical aspects are still unclear and the kinematic and neuromuscular deficiencies associated with the 3 main clinical phenotypes are poorly understood. A validated non-invasive device allows the 3D evaluation of femorotibial rotations during walking.
The diagnostic process is based on clinical examination. The evolution of measuring tools like radios, RMI and kinematics device allows a more precise diagnostic of patellofemoral Pain syndrome. We still don't know what kind of gait parameters could help to categorize the different phenotypes. With a better understanding of these phenotypes the investigators will be able to propose a better personalized rehabilitation. Patellofemoral pain syndrome is defined as an anterior knee pain in front of and around the patella. The diagnosis of patellofemoral pain syndrome is based on clinical examination and standard imaging. The pathophysiology of the patellofemoral pain syndrome is multifactorial involving static and dynamic dysfunctions of the hip, knee and foot, which remain incompletely elucidated to date. The prevalence of patellofemoral pain is high with a high rate of chronicity and recurrence and an overrepresentation of young, athletic and female populations. A pragmatic classification distinguishes 3 main clinical phenotypes of patellofemoral pain syndrome: with objectively displaceable patella, with extra-patellar alignment problems and without alignment problems. The links between the clinic and biomechanics are still unclear and the kinematics and neuromuscular impairments associated with the 3 main clinical phenotypes are poorly understood. The KneeKG is an optoelectronic kinematic assessment device using non-invasive sensors and dedicated to real-time measurement of 3D femoro-tibial position and rotations. The kinematic, neuro-muscular, postural and proprioceptive assessments will allow us to better understand the pathophysiology of the patellofemoral pain syndrome, to establish a more accurate diagnosis of the disease, and provide a better understanding of its causes. Several studies have shown that better adherence to exercise is associated with greater benefit in terms of pain and function in chronic pathologies. Semi-structured interviews will enable the investigators to assess the impact of information derived from kinematic examination of the knees on adherence to treatment.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
45
One EOS exam of lower extremities
Semi-structured interview to identify factors influencing patient adherence behavior for a sub-group of 15 patients. By phone, between 1 to 3 months after inclusion.
Service de Rééducation et de Réadaptation de l'Appareil Locomoteur et des Pathologies du Rachis - Hôpital Cochin
Paris, Île-de-France Region, France
Amplitude of rotation
Amplitude of rotation of the femur with respect to the tibia in the bearing phase in the 3 planes of space
Time frame: Day of inclusion (up to 10 days)
Length measures
EOS femoro-tibial alignment
Time frame: Day of inclusion (up to 10 days)
Q angle (in degree)
EOS femoro-tibial alignment
Time frame: Day of inclusion (up to 10 days)
Varus valgus(in degree)
EOS femoro-tibial alignment
Time frame: Day of inclusion (up to 10 days)
Peak torque (N.m)
Quadriceps isokinetic strenght
Time frame: Day of inclusion (up to 10 days)
Total work (N.m)
Quadriceps isokinetic strenght
Time frame: Day of inclusion (up to 10 days)
Peak torque (N.m)
Hamstrings isokinetic strenght
Time frame: Day of inclusion (up to 10 days)
Total work (N.m)
Hamstrings isokinetic strenght
Time frame: Day of inclusion (up to 10 days)
Quadriceps/Hamstring ratio : 2 measure/leg
Time frame: Day of inclusion (up to 10 days)
Peak torque (N.m)
Hip abductors static strenght
Time frame: Day of inclusion (up to 10 days)
Average torque (N.m)
Hip abductors static strenght
Time frame: Day of inclusion (up to 10 days)
Time for reaching peak (s)
Hip abductors static strenght
Time frame: Day of inclusion (up to 10 days)
Time difference in the onset between the m.vastus lateralis and m.vastus medialis contraction in ms
Activity of the quadriceps measured. Electromyogram was used to quantify the electric potential of quadriceps and referred to as 'quadriceps muscle EMG activity' throughout
Time frame: Day of inclusion (up to 10 days)
Y test
Static and dynamic unipodal balance
Time frame: Day of inclusion (up to 10 days)
Eccentric step-down test
Static and dynamic unipodal balance
Time frame: Day of inclusion (up to 10 days)
Lateral step down test
Static and dynamic unipodal balance
Time frame: Day of inclusion (up to 10 days)
Unipodal stabilometric evaluation
Static and dynamic unipodal balance
Time frame: Day of inclusion (up to 10 days)
Foot posture index
Foot static
Time frame: Day of inclusion (up to 10 days)
Navicular drop test
Foot static
Time frame: Day of inclusion (up to 10 days)
Ober's test
Muscle hypoextensibility. Quadriceps, harmstrings, calves,
Time frame: Day of inclusion (up to 10 days)
Visual Analog Scale
Determine pain / No pain = 0, maximal pain =100
Time frame: Day of inclusion (up to 10 days)
Anterior knee pain scale (AKPS)
Questionnaire to determine pain / 13 questions, minimum score = 0 point, maximum score = 100 points
Time frame: Day of inclusion (up to 10 days)
12-Item Short Form Survey (SF-12)
Quality of life, to determine pain
Time frame: Day of inclusion (up to 10 days)
Semi-structured interview
Semi-structured interview for a sub-group of 15 patients identify factors influencing patient adherence behavior.
Time frame: From month 1 to month 3
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