Clinique Saint-Martin Sport
Marseille, 13000, France
NCT Number: NCT07553013
The goal of this trial is to test if functional proprioceptive stimulations combined with continuous passive movement is more efficient than continuous passive movement alone to recover knee joint mobility after anterior cruciate ligament reconstruction in adults. It will also learn about the influence of functional proprioceptive stimulations on pain and pain medication. The main questions it aims to answer are:
* Does functional proprioceptive stimulations combined with continuous passive movement increase knee joint mobility more than continuous passive movement alone? * Does functional proprioceptive stimulations combined with continuous passive movement reduce perceived pain and pain medication use more than continuous passive movement alone? Researchers will compare functional proprioceptive stimulations combined with continuous passive movement to continuous passive movement alone to see if functional proprioceptive stimulations combined with continuous passive movement is more efficient than continuous passive movement alone.
Participants will:
* Follow a supervised rehabilitation intervention comprising functional proprioceptive stimulations combined with continuous passive movement or continuous passive movement alone during five days a week for 2 weeks * Attend the clinic five days a week for 2 weeks for rehabilitation, checkups and assessments
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Notify Me18 year–55 year
All sexes
Interventional
Not applicable
Marseille, 13000, France
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
5 days a week for 2 weeks
5 days a week for 2 weeks
Time frame: From enrollment to the end of intervention at 2 weeks
Active and passive range of motion of the knee joint (in degrees; °) will be assessed with a 30-cm long manual goniometer at the end of the first session, the fifth and the last rehabilitation session of the 2 weeks intervention.
Time frame: Throughout the 2 weeks intervention
Pain intensity will be assessed using a visual analogue scale (VAS) ranging from 0 (no pain) to 10 (worst imaginable pain). Pain scores will be recorded at the beginning and at the end of each rehabilitation session (n = 10).
Participants will reported daily intake of analgesic medication throughout the two-week rehabilitation period by simpling answering "YES" or "NO".
Universite Cote d'Azur
Other
Bénéfices de la Synchronisation Des Stimulations Proprioceptives Fonctionnelles (FPS) Avec la thérapie Par Mouvements Passifs Continus (CPM) après Reconstruction du Ligament croisé antérieur (RLCA).
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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