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Clinical Trials in Belgium / NCT07523178
Starting soon Not applicable

Effects of a Targeted Prevention Program on Change-of-Direction Biomechanics and Performance in Elite Female Soccer Players

NCT07523178 · tracked via the Priya Life Science Belgium tracker
Phase
Not applicable
Started
2026-03-30
Last updated
2026-04-17

Condition(s) studied

Anterior Cruciate Ligament Injury

Investigational drug(s) / intervention(s)

Targeted Injury Prevention Program

Targeted Injury Prevention Program: A structured injury prevention program integrated into regular soccer training sessions and performed twice per week for six weeks. The program includes exercises targeting neuromuscular control, lower-limb strength, trunk stability, balance, plyometric ability, and change-of-direction technique.

Study summary

Anterior cruciate ligament (ACL) injuries are common in female soccer and frequently occur during change-of-direction (COD) movements without contact. Biomechanical deficits during these movements are considered important risk factors.

This study aims to evaluate the effects of a targeted injury-prevention program on biomechanical movement quality and performance during change-of-direction tasks in female soccer players.

Participants will perform a 90° cutting task during which biomechanical movement quality will be assessed using the Cutting Movement Assessment Score (CMAS), while performance will be evaluated using cutting time measured with photoelectric timing gates. Participants will also perform the 505 Agility Test to assess additional change-of-direction performance.

In addition, subjective perceptions of functional confidence and performance will be collected using Likert-scale questionnaires.

The study will assess whether a structured prevention program integrated into regular training can improve biomechanical movement patterns and change-of-direction performance.

Eligibility

Sex
FEMALE
Min age
13 Years
Max age
16 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Female soccer players aged 13 to 16 years * Female soccer players training at least 3 times per week * Ability to provide informed consent (parental consent required for minors) Exclusion Criteria: * Previous lower-limb surgery * Current musculoskeletal injury * Refusal to participate or withdrawal of consent

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
University of Liège Liège Liège

More University of Liege trials in Belgium

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07523178 on ClinicalTrials.gov ↗ ← All trials in Belgium