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Study identifier: NCT06206200 Synced from ClinicalTrials.gov · July 29, 2026
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The Effects of Cognitive Dual-Tasking in Later Stages of Rehabilitation After ACL Reconstruction

Condition: Anterior Cruciate Ligament Reconstruction · Athrogenic Muscle Responses · ACL Injury  ·  Sponsor: University Ghent

PhaseNA
Planned participants80
Who can joinAll sexes, 18 Years to 40 Years
Healthy volunteersNo

About this study

Anterior cruciate ligament (ACL) injuries are common in sports and often require a long and challenging rehabilitation process. Athletes who sustain these injuries typically engage in pivoting and cutting sports, where these motor tasks must be performed simultaneously with cognitive tasks such as decision-making and keeping an eye on the opponent. Directing attention to both cognitive and motor tasks leads to cognitive-motor interference, which is associated with movement patterns that increase the risk of ACL (re)injury. Therefore, it is crucial that before returning to such demanding sports after ACL reconstruction, athletes sufficiently develop and automate safe yet efficient motor skills to free up attentional capacity for decision-making, thereby reducing the risk of suboptimal movement patterns and reinjury. However, current rehabilitation programs often primarily focus on the motor component in a single-task manner, giving insufficient attention to the cognitive component that is inseparable from sports. This randomized controlled trial aims to investigate the effects of implementing motor-cognitive dual tasks in the end phase rehabilitation after ACL reconstruction on muscle function, functional outcomes, and patient-reported outcomes.

This description comes directly from the study's public registry record.

Talk to the study team

Evy Deschaumes, MSc  ·  +32 9 332 5503  ·  evy.deschaumes@ugent.be

Erik Witvrouw, prof. dr.  ·  +32 9 332 26 32  ·  erik.witvrouw@ugent.be

Always discuss trial participation with your own doctor first.

Locations (1)

AZ Delta Roeselare (Campus Brugsesteenweg)Roeselare, West-Vlaanderen, BelgiumRecruiting

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Source record: clinicaltrials.gov/study/NCT06206200