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Patellofemoral Pain Syndrome clinical trials

View clinical trials related to Patellofemoral Pain Syndrome.

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NCT ID: NCT03998241 Completed - Clinical trials for Proprioceptive Disorders

Joint Position Sense in Individuals With Anterior Knee Pain

Start date: February 1, 2017
Phase:
Study type: Observational [Patient Registry]

Introduction Anterior knee pain (AKP) commonly affects physically active as well as sedentary individuals and the aetiology remains unknown. Altered joint position sense (JPS) impacts accurate motor action and knee joint stability. It is unclear whether people with AKP have altered JPS. The aim of this study was to investigate the JPS of individuals with AKP. Methods A descriptive cross-sectional design was used to measure JPS in twenty-five participants with unilateral or bilateral AKP. The Vicon 3D motion analysis system was used to assess JPS by means of active joint position sense testing during single leg squat and active knee extension in sitting. Target angles were self-determined based on each participant's capabilities. The absolute error (AE) was used as the main outcome measure. Impaired JPS was classified as an AE equal to or greater than five degrees.

NCT ID: NCT03966937 Completed - Clinical trials for Patellofemoral Pain Syndrome

Trigger Point Dry Needling In Patient With Patellofemoral Pain Syndrome

Start date: March 19, 2019
Phase: N/A
Study type: Interventional

This study intends to determine the effects of trigger point dry needling in patients with Patellofemoral pain Syndrome.

NCT ID: NCT03897907 Completed - Clinical trials for Patellofemoral Pain Syndrome

The Effect of Psychologically Informed Education in Adolescents With Patellofemoral Pain

Start date: April 5, 2019
Phase: N/A
Study type: Interventional

This is a randomized prospective study assessing the impact of psychosocial factors on pain and physical performance among adolescents with anterior knee pain. A set of psychosocial surveys assessing activity-related fear, stress, anxiety and depression will be completed by the participant/parents. Participants will then complete clinical tests of physical performance, numeric pain rating scale, and a self-report questionnaire of functional ability. Participants will then be randomized into one of two psychosocial intervention groups (psychologically informed education group and a control group). After participants receive their assigned education intervention, the clinical tests of pain and self-reported functional ability will be readministered. Participants with anterior knee pain will then complete follow-up surveys of their psychosocial beliefs, pain and self-reported functional ability through REDcap at immediately post-intervention, 2 weeks, 6 weeks, and 3 months.

NCT ID: NCT03897569 Completed - Clinical trials for Patellofemoral Pain Syndrome

Association Between Ankle Dorsiflexion and Frontal Projection Angle in PFPS

Start date: March 30, 2019
Phase:
Study type: Observational

The study will investigate an association between ankle dorsiflexion and altered frontal knee kinematics during step down test in patients with PFPS.

NCT ID: NCT03784235 Completed - Clinical trials for Patellofemoral Pain Syndrome

Bone Metabolic Activity in the Patellofemoral Joint in Patients With Unilateral PFP

Start date: January 2, 2019
Phase:
Study type: Observational

This study aims to examine whether individuals with unilateral patellofemoral pain (PFP) have increased subchondral bone remodelling and thus increased 18F Sodium Fluoride (18F-NaF) uptake in the painful knee compared to the opposite knee measured by simultaneous positron emission tomography and computed tomography (PET/CT) and to examine whether the increased uptake is associated with pain intensity, with patient-reported function and with pain localization. Furthermore we aim to investigate the effect of an acute patellofemoral loading bout on the bone remodelling.

NCT ID: NCT03771495 Completed - Clinical trials for Patellofemoral Pain Syndrome

The Immediate Effects of Passive Hip Joint Mobilization on Hip Muscle Strength in Patients With Anterior Knee Pain

Start date: December 21, 2018
Phase: N/A
Study type: Interventional

The aim of the study is to assess the immediate effects of passive hip joint mobilisation (in comparison to a sham mobilisation) on eccentric hip abductor/external rotator muscle strength on the basis of manual muscle testing with a hand-held-dynamometer within a double-blinded cross-over study design. Patients with anterior knee pain and signs of impaired hip function will be recruited in Vienna and surrounding area, measurements/data collection will be conducted by two experienced physiotherapists in a physiotherapy group practice in 1150 Vienna.

NCT ID: NCT03685812 Completed - Clinical trials for Patellofemoral Pain Syndrome

Validity and Reliability of Autocad Software Assessment of JPS in PFPS

Start date: September 25, 2018
Phase:
Study type: Observational

The overall aim of the study is to assess the reliability and validity of Autocad software to measure JPS in PFPS, especially: 1. To assess the intra-tester and between day reliability of measurement of JPS using Autocad software. 2. To assess the validity of these measurements against those found during an IKD.

NCT ID: NCT03663595 Completed - Clinical trials for Patellofemoral Pain Syndrome

Treatment Effects on Neuromuscular Properties on Young Women Symptomatic for Patellofemoral Pain Syndrome

Start date: October 1, 2018
Phase: N/A
Study type: Interventional

Patellofemoral Pain Syndrome (PFPS) is characterized by diffuse pain around the knee joint. This presence of pain is the most common manifestation in sports medicine among adults and young people. Women are more likely to develop PFPS. Among the young adult population, it is estimated that 13% of the women are affected by PFPS. There is a consensus among clinicians that PFPS etiology is multifactorial, including local factors (structures present or acting directly on the patellofemoral joint) and nonlocal factors [extrinsic to the patellofemoral joint, including proximal factors (hip, trunk and pelvis), and distal factors (ankle and foot)]. PFPS is not a degenerative syndrome, and conservative treatment offers good results. However, the most appropriate therapeutic approach is still unclear, and the rate of nonresponders to treatment is high. One of the possible explanations for failure of the therapeutic intervention is that the triggering mechanisms of PFPS are not the same for all subjects, and probably some patients cannot be reached by standard treatment. The traditional intervention model focuses on the strengthening of the knee extensor muscles, but recent literature has pointed out that multi-articular treatment models (i.e., exercises for the proximal or distal factors, in addition to exercises for the quadriceps) have shown better results. It is believed that the elaboration of treatment protocols combining local and non-local factors, present greater responsiveness and results retention, thus reducing treatment failure. Based on this, and due to the lack of experimental studies that aimed to compare the effects of a multi-articular intervention protocol combining local and non-local factors in women affected by PFPS, this study aims to evaluate the effects of two multi-articular intervention protocols based on exercises (1) for the proximal and local factors versus (2) for the distal and local factors on the clinical, functional and neuromechanical outcomes of young women with PFPS. Participants of the PFPS group will be submitted to one of two intervention models for an 12-week rehabilitation program. Model 1 will be composed of exercises focusing on local and proximal PFPS factors, and Model 2 will be composed of exercises focused on the local and distal factors.

NCT ID: NCT03615976 Completed - Clinical trials for Anterior Knee Pain Syndrome

Does Arthroscopic Patellar Denervation With High Tibial Osteotomy Improve Anterior Knee Pain

Start date: March 1, 2017
Phase: N/A
Study type: Interventional

Arthroscopy will be done in all cases before osteotomy to assess lat. Comp and grade of patellofemoral O.A Arthroscopic patellar denervation with vaper or diathermy will be done plus open wedge high tibial osteotomy in one group and other group OWHTO only will be done comparing the rustles of two groups to assess the efficacy of this procedure followed by an average follow up to 12 months. And follow up( 6th weeks ,3rd month ,6th month , 12th month) By clinical examinationan and x-ray and knee scores 1. Scoring of patellofemoral disorders( Kujala) score 2. Knee Injury and Osteoarthritis Outcome Score (KOOS)

NCT ID: NCT03293121 Completed - Clinical trials for Patellofemoral Pain Syndrome

Effect of Strength and Coordination Training on Biomechanics and Injury in New Runners

Start date: January 15, 2017
Phase: N/A
Study type: Interventional

The investigators hypothesize that new runners participating in an 8 week strength and coordination training program prior to beginning to run will 1) display different coordination patterns , and 2) experience fewer injuries, compared to new runners who do not perform strength or coordination training prior to running.