Patello Femoral Pain Syndrome

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Review clinical trials related to Patello Femoral Pain Syndrome. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Effects of Kinesio Taping Versus McConnell Taping on Clinical Outcomes in Patients With Patellofemoral Pain Syndrome.

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). The 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? Participants 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.

Participants needed: 80
Trial details
Age: 18-50Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Jun 26, 2026Locations: 1
Eligibility criteria

Anterior or retropatellar pain for a minimum of 3 months during functional activ... [+3]

Meniscal or ligamentous injury [+3]

Status: Recruiting

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

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/week) 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.

Participants needed: 48
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Ibadat International University, IslamabadUpdated: Jun 26, 2026Locations: 1
Eligibility criteria

Male and female athletes aged 18-40 years [+4]

History of knee surgery or significant knee trauma in the past 6 months [+4]

Status: Not yet recruiting

Ultrasound Examination of the VMO in Patellofemoral Pain Syndrome

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.

Participants needed: 40
Trial details
Age: 18-65Biological sex: AllType: ObservationalSponsor: Hasan Kalyoncu UniversityUpdated: Feb 20, 2026Locations: 1
Eligibility criteria

Between the ages of 18 and 65 [+4]

History of previous surgery on the knee joint [+4]

Status: Not yet recruiting

AI Driven EX Versus Conventional in PFPS

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. The 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 .

Participants needed: 40
Trial details
Age: 18-40Biological sex: AllType: InterventionalSponsor: Cairo UniversityUpdated: Feb 12, 2026Locations: 2
Eligibility criteria

Their ages range from 18- 40 years old, including both genders (male & female). [+2]

Any congenital deformity of the lower limb, [+3]