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Patellofemoral Pain Syndrome clinical trials

View clinical trials related to Patellofemoral Pain Syndrome.

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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: NCT03620799 Not yet recruiting - Clinical trials for Anterior Knee Pain Syndrome

Efffectiveness of a Roller Intervention in Anterior Knee Pain

Start date: August 15, 2018
Phase: N/A
Study type: Interventional

Anterior knee pain is one of the most frequent reasons for consultation within knee conditions in adolescents and young adults. However, despite the high prevalence of this disorder, its pathogenesis and therefore its treatment are not clearly understood. Foam rolling has become a common intervention to enhance joint mobility and muscle recovery after exercise. the aim of this study is analyze the effectiveness of a roller intervention in patients with anterior knee pain.

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: NCT03468491 Not yet recruiting - Clinical trials for Patellofemoral Pain Syndrome

The Additional Effect of Hallux Valgus Correction on Runners With First Ray Instability and Patellofemoral Pain Syndrome

Start date: June 20, 2018
Phase: N/A
Study type: Interventional

The study purpose is to investigate the effectiveness of a program combining biomechanical taping with lower extremity neuromuscular exercises for runners with patellofemoral pain syndrome (PFPS) and hallux valgus

NCT ID: NCT03450824 Terminated - Clinical trials for Patellofemoral Pain Syndrome

Relationship Between Constitutional Varus Knee and Patellofemoral Pain

Start date: March 23, 2018
Phase:
Study type: Observational

This study aims to research on the relationship between constitutional varus knee and patellofemoral pain. The standardized standing whole-lower-extremity radiographs, the knee lateral view and skyline view of the participants will be taken. The hip-knee-ankle angle will be obtained from the radiographs. According to the hip-knee-ankle angle, the knees will be labelled knee varus or knee nonvarus. The knee varus incidences of the two groups will be determined and compared.

NCT ID: NCT03364855 Recruiting - Clinical trials for Patellofemoral Pain Syndrome

Star Excursion Balance for Patellofemoral Pain Syndrome

SEBT
Start date: January 12, 2018
Phase: N/A
Study type: Interventional

Patellofemoral pain syndrome (PFPS) is a common and painful musculoskeletal condition that affects physically active young adults and causes pain front of the knee. Patients with PFPS has bilateral impairment in proprioception, as well as more in the affected knee than the normal; also the decrease of muscular strength, range of motion, and neuromuscular control are known to result with impaired static and dynamic balance.This study aimed to investigate the efficacy of a-four week YDT balance exercises on pain, quality of life and functional state in patients with PFPS with impaired balance.

NCT ID: NCT03324204 Recruiting - Clinical trials for Patellofemoral Pain Syndrome

Shock Wave Therapy Versus Neuromuscular Training in Women With Patellofemoral Pain

Start date: August 1, 2014
Phase: N/A
Study type: Interventional

The aim of the trial is to compare the efficacy of extracorporeal shock wave therapy (ESWT) versus neuromuscular training (TR) in reducing pain in women with patellofemoral pain (PFP). Women with PFP will be randomly divided into two therapeutic groups: ESWT and TR. The ESWT group will undergo extracorporeal shock wave therapy to the iliotibial band and tensor fascia latae. The TR group will be treated with neuromuscular training. The women's gait will be analysed and the strength of hip abductors and internal rotators will be measured. Additionally, the women's pain and health status will be assessed with the visual analogue scale and the Lysholm Scale. Outcomes will be registered at baseline, and then at five weeks and at three months post-therapy

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.

NCT ID: NCT03285464 Completed - Clinical trials for Patellofemoral Pain Syndrome

Utilizing the Trunk as a Proximal Lever to Strengthen the Hip Musculature and Alter Lower Extremity Function

Start date: August 9, 2017
Phase: N/A
Study type: Interventional

Does a rotary based triplanar exercise intervention that utilizes the trunk as a proximal lever, strengthen the hip and alter dynamic LE alignment in running females?