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After reconstruction of the anterior cruciate ligament, the aim for the vast majority of sportspeople is to return to the field. To date, 65% of patients who have undergone ACL rehabilitation return to their previous level, and 55% return to competition. To achieve this, physiotherapy sessions need to prepare the return to sport as well as possible, by simulating the cognitive demands (reading the game, double task, etc.) that might be encountered on the pitch. Tests to assess the athlete's performance do exist, in order to optimise this return to sport, but they do not include the cognitive tasks that are present in sport. The high cognitive demands of the sporting environment therefore justify the inclusion of cognitive tasks in these return to sport tests. The aim of this research is to assess the impact of the cognitive task on the performance of a return to sport test following ACL reconstruction. Patients who have undergone ACL reconstruction and healthy subjects will therefore be given a return to sport test called the 'Single Leg Hop for Distance' with and without a cognitive task in order to observe the influence of the cognitive task on the results of the hop.
Including healthy subjects in this study will make it possible to study the impact of the cognitive task in these subjects, who have no neurophysiological dysfunction linked to ACL reconstruction.
The aim of this study is therefore to try to develop the return to sport tests currently described in the literature by proposing a new, improved test that takes account of the cognitive dimension, which is omnipresent in the sporting environment.
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Inclusion and exclusion criteria
The inclusion criteria for the test group (patients with ACL reconstruction) were as follows :
Patients meeting all these inclusion criteria will be included in the study.
Thus, for the test group, the non-inclusion criteria to be taken into account are as follows:
Finally, for the test group, the exclusion criteria to be taken into account are as follows:
For the control group (healthy persons), the inclusion criteria are similar to those for the test group. They correspond to :
Persons meeting all these inclusion criteria will be included in the study.
Thus, for the control group, the non-inclusion criteria are as follows:
Finally, the exclusion criteria for this group correspond to :
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31 participants in 8 patient groups
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Central trial contact
Simon SV VALOT; Florian FF FORELLI
Data sourced from clinicaltrials.gov
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