The objective of the study is to compare, with or without wearing an elastic proprioceptive knee brace, the functional proprioceptive capacity of the knee in patients suffering from proprioceptive deficit.
This proprioceptive deficit is found following various traumas or injuries such as Anterior Cruciate Ligament (ACL) rupture, for example. The use of joint stabilizers (such as knee braces) will allow an increase in sensory input (particularly at the level of cutaneous mechanoreceptors), and improve the biomechanics of the injured joint. The objective of the study is to compare, with or without wearing an elastic proprioceptive knee brace, the functional proprioceptive capacity of the knee in patients suffering from proprioceptive deficit.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
15
the patient will perform the tests with the knee brace
the patient will perform the tests without the knee brace
Clinique de la sauvegarde
Lyon, France
Comparison of the functional proprioceptive capacity of the knee in patients with proprioceptive deficit with or without wearing an elastic proprioceptive knee brace.
The functional proprioceptive capacity of the knee is measured via the 3-axis composite score of the Y Balance Test (YBT). This score corresponds to the average of the 3 maximum distances obtained during the YBT test, normalized by leg length.
Time frame: Day 1 (2 times, after condition 1 and after condition 2)
Evaluation of tactile sensitivity (baresthesia) with or without wearing the knee brace
Tactile sensitivity (Baresthesia) via the use of Weinstein monofilaments.
Time frame: Day 1 (2 times, after condition 1 and after condition 2)
Evaluation of the sensitivity to the position of a joint with or without wearing the knee brace
Sensitivity to the position of a joint by determining the perception of the position of the leg in space via the JPS (Joint Position Sense) test.
Time frame: Day 1 (2 times, after condition 1 and after condition 2)
Evaluation of the static stability when using or not the knee brace.
Static stability level is measured by Visual Analogic Scale (VAS) completed by the patient : 0 corresponds to no stability (worst outcome) and 10 to maximum stability (better outcome).
Time frame: Day 1 (2 times, after condition 1 and after condition 2)
Evaluation of the stability when walking when using or not the knee brace.
Stability level when walking is measured by Visual Analogic Scale (VAS) completed by the patient : 0 corresponds to no stability (worst outcome) and 10 to maximum stability (better outcome).
Time frame: Day 1 (2 times, after condition 1 and after condition 2)
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Evaluation of the discomfort level when using or not the knee brace.
Discomfort level when walking is measured by Visual Analogic Scale (VAS) completed by the patient : 0 corresponds to no discomfort (better outcome) and 10 to maximum discomfort (worst outcome).
Time frame: Day 1 (2 times, after condition 1 and after condition 2)
Evaluation of the fluidity level when using or not the knee brace.
Fluidity level is measured by Visual Analogic Scale (VAS) completed by the patient : 0 corresponds to no fluidity (worst outcome) and 10 to maximum fluidity (better outcome).
Time frame: Day 1 (2 times, after condition 1 and after condition 2)
Evaluation of the range of motion ok the knee level when using or not the knee brace.
Range of motion of the knee level is measured by Visual Analogic Scale (VAS) completed by the patient : 0 corresponds to no range of motion (worst outcome) and 10 to maximum range of motion (better outcome).
Time frame: Day 1 (2 times, after condition 1 and after condition 2)
Evaluation of patient satisfaction with the use of the knee brace with a specific questionnaire
Patient satisfaction with the use of the knee brace via a specific questionnaire composed of 15 questions.
Time frame: Day 1
Evaluation of the patient's tolerance to the use of the knee brace.
Evaluation of the patient's tolerance to the use of the knee brace through the collection of adverse events.
Time frame: Day 1