Actively Recruiting

Phase Not Applicable
Age: 17Years - 20Years
All Genders
Healthy Volunteers
NCT07019727

ESSKA/ESMA ACL Injury Prevention Program in Czech Sport

Led by Masaryk University · Updated on 2025-09-30

100

Participants Needed

1

Research Sites

81 weeks

Total Duration

On this page

Sponsors

M

Masaryk University

Lead Sponsor

B

Brno University Hospital

Collaborating Sponsor

AI-Summary

What this Trial Is About

This study aims to address the rising incidence of ACL injuries, particularly among adolescents, by developing and implementing a comprehensive prevention program based on the evidence-based "ACL Prevention for ALL" framework recommended by ESSKA-ESMA. The project focuses on muscle strengthening, flexibility, coordination, proper movement techniques, and a multidisciplinary approach involving coaches, physiotherapists, and physicians. Through targeted exercise modules, education, and dynamic evaluation-including 2D motion analysis-the study seeks to reduce ACL injuries, enhance movement safety, and enable individualized training plans by identifying and correcting muscle and biomechanical imbalances.

CONDITIONS

Official Title

ESSKA/ESMA ACL Injury Prevention Program in Czech Sport

Who Can Participate

Age: 17Years - 20Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Participants aged 17 to 20 years
  • Actively engaged in sports with a high risk of ACL injury
  • No or minimal previous knee injuries that do not limit current physical activity
  • Willingness to participate in the prevention program including regular training and assessments
  • Signed informed consent for participation and testing; for minors, consent from legal guardians
Not Eligible

You will not qualify if you...

  • Current knee joint injury requiring treatment or surgery
  • Chronic diseases or conditions affecting injury prevention outcomes (e.g., congenital abnormalities, neuromuscular disorders, cardiovascular diseases)
  • Unable or unwilling to provide written informed consent
  • Irregular participation in training program or assessments

AI-Screening

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Trial Site Locations

Total: 1 location

1

Faculty of Medicine, Masaryk University

Brno, Czechia, 62700

Actively Recruiting

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Research Team

M

Michael Lujc, MUDr.

CONTACT

F

Filip Huceček, MUDr.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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