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Comparing the Effectiveness of Kinesio Taping and Knee Orthosis in Patients With Patellofemoral Pain Syndrome

Not Applicable
Completed
Conditions
Anterior Knee Pain Syndrome
Patellofemoral Syndrome
Kinesiotape
Patellofemoral Pain Syndrome
Patellofemoral Pain
Orthotic Devices
Interventions
Procedure: Orthosis
Procedure: Kinesio taping
Procedure: Control
Registration Number
NCT05995210
Lead Sponsor
Istanbul Medipol University Hospital
Brief Summary

The aim of the study is to compare the efficacy of kinesio taping treatment and knee orthosis treatment in Patellofemoral Pain Syndrome (PFAS). 54 patients were included in the study and the patients were divided into 3 groups as kinesio taping group (KTG) (n=18), orthotics group (OG) (n=18) and control group (CG) (n=18). A progressive exercise program was applied to all groups and patients were treated 2 days a week for 6 weeks.While kinesio taping was applied to KTG in each session, knee orthosis was given to OG and they were asked to use it for 6 weeks. Visual Analogue Scale (VAS), Kujala Score, Knee injury and Osteoarthritis Outcome Score (KOOS), isokinetic strength test (IST) and joint position sense (JPS) test were used in the evaluation.

Detailed Description

Patients were divided into 3 groups as patellofemoral knee orthosis group, kinesio taping group and control group. Randomization of group allocation was done using the website "https://www.randomizer.org". Patients were unaware of the other group's treatment program and group allocation. All participants signed an informed consent form before the study. The primary outcome measure of our study was the Kujala Score, and the secondary outcome measures were the Knee Injury and Osteoarthritis Outcome Score (KOOS), Visual Analog Scale (VAS), quadriceps and hamstring isokinetic muscle strength, and knee joint position sense. The evaluations were performed before and after treatment. All patients were informed about the disease and treatment process before treatment. Patients were informed about the things they should pay attention to for pain management in daily life activities and suggestions were made. In addition, all patients received at least 2 weeks of NSAID treatment by the orthopedist. A progressive exercise program was applied to all treatment groups. The progressive exercise program was continued under the supervision of a physiotherapist 2 days a week for 6 weeks. The progressive exercise program consisted of strengthening exercises for the muscles around the knee and hip, stretching exercises for the hamstring and gastrosoleus muscles. The knee orthosis group received the OrthoCare® 6158 Genucare Luxa knee orthosis. T-max Kinesiology Tape® (Tmax Medical Co., South Korea) brand kinesio tape was used in all patients. In kinesio tape application, 2 Y-shaped tapes were used. The activation technique was applied to the VMO muscle with the first band. In the second band, mechanical correction technique was applied to the patella.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
54
Inclusion Criteria
  • Be between the ages of 18-45
  • Patients with a body mass index (BMI) less than 29.9
  • Anterior knee pain defined as 3 points on the 10 cm Visual Analogue Scale when performing at least two activities of sitting for a long time, climbing/descending stairs, squatting, running and jumping
Exclusion Criteria
  • Patients with knee osteoarthritis
  • History of surgery involving the lower extremity
  • Patellar or quadriceps tendinopathy
  • Injury to the meniscus or knee ligaments
  • Patients showing an allergic response to kinesio tape
  • Patients previously treated with PFAS
  • Existing hip pathologies
  • History of patellar subluxation or dislocation
  • Patients with neurological disorders
  • Patients who did not fill out the voluntary consent form

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Orthosis groupOrthosisIn addition to the standard exercise program, they were asked to use a knee orthosis for 6 weeks.
Orthosis groupControlIn addition to the standard exercise program, they were asked to use a knee orthosis for 6 weeks.
Kinesio taping groupControlIn addition to the standard exercise program, kinesio taping was applied to the knee for 6 weeks.
Control groupControlA standard exercise program was applied for 6 weeks.
Kinesio taping groupKinesio tapingIn addition to the standard exercise program, kinesio taping was applied to the knee for 6 weeks.
Primary Outcome Measures
NameTimeMethod
Change in baseline Kujala scores of patients treated at week 66 weeks

It is a score that evaluates symptoms and function in patients with patellofemoral pain syndrome. Patients were asked to complete this score before starting the treatment and again at the end of the 6-week treatment.

Secondary Outcome Measures
NameTimeMethod
Change in baseline Knee Injury and Osteoarthritis Outcome Score of patients treated at week 66 weeks

Knee Injury and Osteoarthritis Outcome Score (KOOS) is a score used to evaluate symptoms and functional status related to knee injury and knee osteoarthritis. Patients were asked to complete this score before starting the treatment and again at the end of the 6-week treatment.

Change in baseline isokinetic strength test of patients treated at week 66 weeks

This test is a strength test performed with an isokinetic strength testing machine. This test was applied to the patients before starting the treatment and at the end of the 6-week treatment.

Change in baseline Visual Analogue Scale of patients treated at week 66 weeks

It is a scale that evaluates pain. Patients were asked to complete this scale before starting the treatment and again at the end of the 6-week treatment.

Trial Locations

Locations (1)

Istanbul Medipol University

🇹🇷

Istanbul, Turkey

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