Comparing the Effectiveness of Kinesio Taping and Knee Orthosis in Patients with Patellofemoral Pain Syndrome: a Randomized Controlled Study
Kinesio taping
+ Control
+ Orthosis
Joint Diseases
+ Musculoskeletal Diseases
+ Patellofemoral Pain Syndrome
Supportive Care Study
Summary
Study start date: December 9, 2021
Actual date on which the first participant was enrolled.This study is investigating the effectiveness of two different methods, Kinesio taping and knee braces, in treating patients with patellofemoral pain syndrome, a condition that causes pain in the front of the knee. Participants are divided into three groups: one using knee braces, another using Kinesio tape, and a control group. The aim is to determine which method is more effective in reducing knee pain and improving knee function. Addressing patellofemoral pain is crucial as it can hinder daily activities and lower the quality of life, and finding the best treatment option could significantly benefit those affected. Participants in the study follow a structured exercise program to strengthen and stretch the muscles around the knee and hip, under the guidance of a physiotherapist. The knee brace group uses the OrthoCare® 6158 Genucare Luxa knee orthosis, while the Kinesio tape group uses T-max Kinesiology Tape® for specific taping techniques on the knee. Participants' progress is evaluated using several methods including the Kujala Score and other assessments for pain and muscle strength. Each participant also receives advice on pain management and a short course of medication. Evaluations occur before and after treatment to assess the effectiveness of each method.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.54 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Supportive Care Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Any sex
Biological sex of participants that are eligible to enroll.From 18 to 45 Years
Range of ages for which participants are eligible to join.Healthy volunteers allowed
If individuals who are healthy and do not have the condition being studied can participate.Conditions
Pathology
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.3 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
ExperimentalGroup III
Active ComparatorStudy Objectives
Primary Objectives
Secondary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
Istanbul Medipol University
Istanbul, Turkey (Türkiye)Open Istanbul Medipol University in Google Maps