[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"patello-femoral-pain-syndrome\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:patello-femoral-pain-syndrome":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,4,0,[8,54,82,111],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":34,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":42,"lastUpdatePostDateStruct":43,"startDateStruct":46,"completionDateStruct":48,"leadSponsor":50,"locationsCount":53},"100644562","effects-of-kinesio-taping-versus-mcconnell-taping-on-clinical-outcomes-in-patients-with-patellofemoral-pain-syndrome-100644562",false,"NCT07671482","Effects of Kinesio Taping Versus McConnell Taping on Clinical Outcomes in Patients With Patellofemoral Pain Syndrome.","Effects of Kinesio Taping Versus McConnell Taping on Clinical Outcomes in Patients With Patellofemoral Pain Syndrome. A Randomized Clinical Trial.","PFPS","Inclusion Criteria:\n\n* Anterior or retropatellar pain for a minimum of 3 months during functional activities.\n* 18-50 years of age.\n* Minimum pain of 3\u002F10 on the VAS score.\n* No LL physical therapy in the past 3 months.\n\nExclusion Criteria:\n\n* Meniscal or ligamentous injury\n* Neurological or systemic conditions affecting proprioception, coordination and balance.\n* Spinal referred pain or rheumatoid arthritis.\n* Hip and ankle disorders.","ALL","18 Years","50 Years",{"count":21,"type":22},80,"ESTIMATED","INTERVENTIONAL",[25],"NA","The primary goal of this randomized clinical trial (RCT) is to evaluate whether Kinesio Taping versus McConnell Taping, when integrated into a standardized hip-knee strengthening and neuromuscular control program, produces significant effects in individuals aged 18-50 with patellofemoral pain syndrome (PFPS).\n\nThe main question it aims to answer is: Does Kinesio Taping compared with McConnell Taping when both combined with a standardized hip-knee exercise program, produce different effects on quadriceps neuromuscular activation (VMO-VL sEMG), pain, functional knee pain, and dynamic knee valgus over a 6 week period intervention?\n\nParticipants will be divided into three groups for comparison: the control group will receive a structured hip-knee physical therapy exercise program without any taping intervention, Kinesio Taping group with a standardized exercise program, and a McConnell Taping group with a standardized exercise program.",[28,29,15,30,31,32,33],"Patello Femoral Pain Syndrome","Anterior Knee Pain Syndrome","Patellofemoral Pain Syndrome","Patellofemoral Disorder","Patellofemoral Pain, PFP","Patellofemoral Pain (PFPS)",[35,36,37,38,39,30,40],"Electromyography","EMG","Kinesio Taping","McConnell Taping","Exercise Therapy","Single-Leg Squat","RECRUITING","2026-06-25",{"date":44,"type":45},"2026-06-26","ACTUAL",{"date":47,"type":22},"2026-06",{"date":49,"type":22},"2026-10",{"name":51,"class":52},"Cairo University","OTHER",1,{"id":55,"slug":56,"hasResults":11,"nctId":57,"briefTitle":58,"officialTitle":59,"acronym":60,"eligibilityCriteria":61,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":62,"enrollmentInfo":63,"targetDuration":4,"studyType":23,"phases":65,"briefSummary":66,"conditions":67,"keywords":68,"overallStatus":41,"whyStopped":4,"lastUpdateSubmitDate":74,"lastUpdatePostDateStruct":75,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":53},"100637264","comparative-effects-of-blood-flow-restriction-resistance-training-versus-blood-flow-restriction-cycling-on-pain-quadriceps-strength-and-functional-outcomes-in-athletes-with-patellofemoral-pain-100637264","NCT07585305","Comparative Effects of Blood Flow Restriction Resistance Training Versus Blood Flow Restriction Cycling on Pain, Quadriceps Strength, and Functional Outcomes in Athletes With Patellofemoral Pain","Comparative Effects of Blood Flow Restriction Resistance Training Versus Blood Flow Restriction Cycling on Pain, Quadriceps Strength, and Functional Outcomes in Athletes With Patellofemoral Pain: A Randomized Controlled Trial","BFR-PFP-RCT","Inclusion Criteria:\n\n1. Male and female athletes aged 18-40 years\n2. Clinically diagnosed with patellofemoral pain syndrome\n3. Anterior or retropatellar knee pain of at least 3 months duration\n4. Pain provoked by at least two functional activities (e.g., squatting, stair climbing, running, prolonged sitting)\n5. Willingness to participate and provide written informed consent\n\nExclusion Criteria:\n\n1. History of knee surgery or significant knee trauma in the past 6 months\n2. Presence of ligament, meniscal, or cartilage injuries\n3. Neurological, vascular, or systemic inflammatory conditions\n4. Contraindications to BFR training (e.g., deep vein thrombosis, uncontrolled hypertension)\n5. Pregnancy","40 Years",{"count":64,"type":22},48,[25],"This randomized controlled trial compares blood flow restriction (BFR) resistance training (leg press and seated knee extension at 30% 1RM) versus BFR cycling (stationary cycling at low resistance) in 60 athletes (aged 18-40 years) diagnosed with patellofemoral pain syndrome. Both interventions are delivered over 8 weeks (3 sessions\u002Fweek) with a pneumatic cuff set at 80% limb occlusion pressure. Primary outcomes include pain intensity (NPRS), quadriceps strength (handheld dynamometer), and functional ability (Kujala Anterior Knee Pain Scale), assessed at baseline and post-intervention.",[28],[69,70,71,72,73],"Patellofemoral pain","Blood flow restriction training","Quadriceps strength","Athletic Performance","resistance training","2026-06-23",{"date":44,"type":45},{"date":77,"type":45},"2026-05-10",{"date":79,"type":22},"2026-07-25",{"name":81,"class":52},"Ibadat International University, Islamabad",{"id":83,"slug":84,"hasResults":11,"nctId":85,"briefTitle":86,"officialTitle":87,"acronym":4,"eligibilityCriteria":88,"healthyVolunteers":89,"sex":17,"minAge":18,"maxAge":90,"enrollmentInfo":91,"targetDuration":4,"studyType":93,"phases":4,"briefSummary":94,"conditions":95,"keywords":98,"overallStatus":102,"whyStopped":4,"lastUpdateSubmitDate":103,"lastUpdatePostDateStruct":104,"startDateStruct":106,"completionDateStruct":108,"leadSponsor":109,"locationsCount":53},"100625646","ultrasound-examination-of-the-vmo-in-patellofemoral-pain-syndrome-100625646","NCT07425340","Ultrasound Examination of the VMO in Patellofemoral Pain Syndrome","Ultrasonography Examination of the Vastus Medialis Obliquus and Vastus Medialis Longus Muscles in Patellofemoral Pain Syndrome","Inclusion Criteria:\n\n* Between the ages of 18 and 65\n* Have had localized pain in the front of the knee for at least the past 3 months\n* Experience pain during activities that require stair climbing, squatting, prolonged sitting, or knee flexion\n* Have been diagnosed with patellofemoral pain syndrome based on clinical evaluation\n* Volunteer to participate in the study and sign the informed consent form\n\nExclusion Criteria:\n\n* History of previous surgery on the knee joint\n* History of significant trauma to the knee region within the last 6 months\n* Diagnosis of meniscus, ligament injuries, knee osteoarthritis, or inflammatory rheumatic disease\n* Neurological diseases or systemic diseases affecting the musculoskeletal system\n* Presence of other lower extremity pathologies causing pain at a level that could affect measurements",true,"65 Years",{"count":92,"type":22},40,"OBSERVATIONAL","The aim of this study is to examine in detail the ultrasonographic characteristics of the vastus medialis obliquus and vastus medialis longus muscles in individuals with patellofemoral pain syndrome and to compare these findings with those of healthy individuals. It is anticipated that the results obtained will contribute to a better understanding of the muscle-based mechanisms of PFAS and provide a scientific basis for the development of muscle-specific assessment and intervention strategies in physical therapy and rehabilitation practices.",[96,97,28],"Vastus Medialis","Ultrasonographic",[99,100,101],"Patellofemoral Pain","Vastus Medialis Obliqus","Ultrasonographic measurement","NOT_YET_RECRUITING","2026-02-13",{"date":105,"type":45},"2026-02-20",{"date":107,"type":22},"2026-02-25",{"date":42,"type":22},{"name":110,"class":52},"Hasan Kalyoncu University",{"id":112,"slug":113,"hasResults":11,"nctId":114,"briefTitle":115,"officialTitle":116,"acronym":117,"eligibilityCriteria":118,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":62,"enrollmentInfo":119,"targetDuration":4,"studyType":23,"phases":120,"briefSummary":121,"conditions":122,"keywords":4,"overallStatus":102,"whyStopped":4,"lastUpdateSubmitDate":123,"lastUpdatePostDateStruct":124,"startDateStruct":126,"completionDateStruct":128,"leadSponsor":130,"locationsCount":131},"100624084","ai-driven-ex-versus-conventional-in-pfps-100624084","NCT07405034","AI Driven EX Versus Conventional in PFPS","Artificial Intelligence Driven Exercises Versus Conventional Exercises Therapy for Patellofemoral","AI- PFPS","Inclusion Criteria:\n\n* Their ages range from 18- 40 years old, including both genders (male \\& female).\n* Their BMI will be ≤ 29 kg\u002Fm2.\n* A traumatic knee pain persisting for at least three months.\n\nExclusion Criteria:\n\n* Any congenital deformity of the lower limb,\n* Any recent injuries and surgeries\n* severe foot deformities such as hallux valgus and claw toe\n* Neuromuscular and neurological disorders.- history of patellofemoral dislocation, subluxation .",{"count":92,"type":22},[25],"This study aims to investigate and compare the effect of AI driven exercises program versus the conventional exercises therapy program on pain, function and dynamic knee valgus angle in treatment of patellofemoral pain syndrome.This study is randomized controlled trial and includes 40 participants .These participants divided into 2 groups (A, B), each group will be assessed with 3 measurments (vas ,dynamic knee valgus, Kujala Anterior Knee Pain Scale) and each group will receive difeerent treatments.\n\nThe individuals in group A(study group) will preceive AI driven exercises program while the individual in group B will receive conventional exercises therapy program. Participants in the both groups are prescribed a 6-week comprehensive exercises program (3 sessions per week) day after day and assessment procedure will be performed pre and post treatmeant .",[28],"2026-02-09",{"date":125,"type":45},"2026-02-12",{"date":127,"type":22},"2026-02-26",{"date":129,"type":22},"2027-01-01",{"name":51,"class":52},2]