EPICInjury Prevention in Youth and Adult Amateur Football via Knee Control+
Support intervention for the use of Knee Control+
+ Information about Knee Control+
Prevention Study
Summary
Study start date: March 25, 2025
Actual date on which the first participant was enrolled.The study aims to prevent injuries among youth and adult amateur football players during the 2025 football season. It focuses on teaching football coaches and players exercises from the Knee Control+ program to reduce injuries. Fitness coaches from an organization called Friskis&Svettis will lead the intervention by educating football coaches through workshops and site visits. This study is essential as it seeks to lower injury rates, allowing players to remain active and healthy throughout the season. By involving club representatives and coaches in the development of support materials, the study ensures the interventions are practical and tailored to the needs of the participants. Participants, including football coaches and players, will engage in workshops and training sessions focused on injury prevention exercises. The study will collect data using online surveys to evaluate the effectiveness of the interventions on injury rates and training behaviors. It will look at how often teams use the Knee Control+ exercises and track injury occurrences throughout the season. The study will compare groups receiving the program against those who do not to determine the success of the intervention. Coaches and players provide feedback throughout the process, ensuring the approach is continually refined and effective.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.1600 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Prevention 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.Over 10 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.Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.2 intervention groups are designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalGroup II
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