MedPath

Kinematic and Neuromuscular Deficiencies Phenotypes Associated with Patellofemoral Pain Syndrome

Not Applicable
Completed
Conditions
Patellofemoral Pain Syndrome
Interventions
Other: EOS Radiation
Behavioral: Semi-structured interview
Registration Number
NCT05441332
Lead Sponsor
Assistance Publique - Hôpitaux de Paris
Brief Summary

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.

Detailed Description

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.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
45
Inclusion Criteria
  • Medical diagnosis of SDFP :
  • Anterior pain of the knee, mechanical, in front of and around the patella noted at more than 3/10 on a simple numerical scale (ligament or meniscal damage, synovial plicae, tendinopathies, apophysitis, neuromas, and osteoarthritis FT are differential diagnoses),
  • Pain during any of the following activities: Going up / down stairs, squats, jumps, jogging, sitting, crouching.
  • Duration of knee anterior pain greater than 1 month
  • Affiliation to a social insurance
  • Signature of the consent to participate
Exclusion Criteria
  • Neurological disorders affecting the lower extremities
  • Radiographic FT osteoarthritis
  • History of surgery or trauma to the lower limb less than 1 year old
  • Intra-articular knee infiltration ≤ 2 months
  • Cognitive or behavioral problems making it impossible to assess
  • Participates in intervention research or is in the exclusion period following a previous research, if applicable
  • Unable to speak, read and write French
  • Patients under guardianship or curatorship,
  • Patients receiving AME (French State Medical aid)

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Patellofemoral pain syndromeEOS RadiationKinematic and neuromuscular assessment
Patellofemoral pain syndromeSemi-structured interviewKinematic and neuromuscular assessment
Primary Outcome Measures
NameTimeMethod
Amplitude of rotationDay of inclusion (up to 10 days)

Amplitude of rotation of the femur with respect to the tibia in the bearing phase in the 3 planes of space

Secondary Outcome Measures
NameTimeMethod
Total work (N.m)Day of inclusion (up to 10 days)

Hamstrings isokinetic strenght

Average torque (N.m)Day of inclusion (up to 10 days)

Hip abductors static strenght

Length measuresDay of inclusion (up to 10 days)

EOS femoro-tibial alignment

Varus valgus(in degree)Day of inclusion (up to 10 days)

EOS femoro-tibial alignment

Time for reaching peak (s)Day of inclusion (up to 10 days)

Hip abductors static strenght

Q angle (in degree)Day of inclusion (up to 10 days)

EOS femoro-tibial alignment

Peak torque (N.m)Day of inclusion (up to 10 days)

Hip abductors static strenght

Quadriceps/Hamstring ratio : 2 measure/legDay of inclusion (up to 10 days)
Eccentric step-down testDay of inclusion (up to 10 days)

Static and dynamic unipodal balance

Lateral step down testDay of inclusion (up to 10 days)

Static and dynamic unipodal balance

Navicular drop testDay of inclusion (up to 10 days)

Foot static

Visual Analog ScaleDay of inclusion (up to 10 days)

Determine pain / No pain = 0, maximal pain =100

Anterior knee pain scale (AKPS)Day of inclusion (up to 10 days)

Questionnaire to determine pain / 13 questions, minimum score = 0 point, maximum score = 100 points

Unipodal stabilometric evaluationDay of inclusion (up to 10 days)

Static and dynamic unipodal balance

Foot posture indexDay of inclusion (up to 10 days)

Foot static

Semi-structured interviewFrom month 1 to month 3

Semi-structured interview for a sub-group of 15 patients identify factors influencing patient adherence behavior.

Time difference in the onset between the m.vastus lateralis and m.vastus medialis contraction in msDay of inclusion (up to 10 days)

Activity of the quadriceps measured. Electromyogram was used to quantify the electric potential of quadriceps and referred to as 'quadriceps muscle EMG activity' throughout

Y testDay of inclusion (up to 10 days)

Static and dynamic unipodal balance

Ober's testDay of inclusion (up to 10 days)

Muscle hypoextensibility. Quadriceps, harmstrings, calves,

12-Item Short Form Survey (SF-12)Day of inclusion (up to 10 days)

Quality of life, to determine pain

Trial Locations

Locations (1)

Service de Rééducation et de Réadaptation de l'Appareil Locomoteur et des Pathologies du Rachis - Hôpital Cochin

🇫🇷

Paris, Ile de France, France

© Copyright 2025. All Rights Reserved by MedPath