The main objective of this study is to evaluate via a physiological analysis of the movements involved in standing, the level of forward flexion of the spine (in cm on the horizontal axis) obtained with the apparatus "Tina" and to compare levels obtained in the same patients with stander/transfer devices "Turner" and "Vertic'Easy".
Secondary objectives of this study are to compare the three devices in terms of: * the level recovery of the spine on the vertical axis (vertical displacement C7, cm) * standing time, defined by the time between the start of the forward flexion and the beginning of the vertical stabilization phase (seconds) * the success rate of the verticalization of the patient (the attempt is considered successful when the vertical position is held for 10 seconds).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
NONE
Enrollment
30
Included patients had never used any of the three devices evaluated in this study. Therefore the patient will make two attempts at standing on each device to enable him/her to get used to the device at the first attempt. A video recording will be made from a camera positioned laterally. Only the results of the second attempt will be a kinematic analysis and will be used for analyzes.
Included patients had never used any of the three devices evaluated in this study. Therefore the patient will make two attempts at standing on each device to enable him/her to get used to the device at the first attempt. A video recording will be made from a camera positioned laterally. Only the results of the second attempt will be a kinematic analysis and will be used for analyzes
CHU de Nîmes - Hôpital Universitaire Carémeau
Nîmes, France
Level of forward flexion of the spine (position of maximum horizontal displacement of C7)
cm
Time frame: Baseline (Day 0; cross-sectional study)
Level of standing (maximum vertical displacement C7)
cm
Time frame: Baseline (Day 0; transversal study)
Angle of hip flexion (angle formed by the line connecting the acromion and the greater trochanter with the line connecting the greater trochanter and the lateral femoral condyle)
degrees
Time frame: Baseline (Day 0; transversal study)
Standing time (time from start of forward flexion and the beginning of the vertical stabilization phase)
seconds
Time frame: Baseline (Day 0; transversal study)
Verticalization achieved (yes/no)
yes/no
Time frame: Baseline (Day 0; transversal study)
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Included patients had never used any of the three devices evaluated in this study. Therefore the patient will make two attempts at standing on each device to enable him/her to get used to the device at the first attempt. A video recording will be made from a camera positioned laterally. Only the results of the second attempt will be a kinematic analysis and will be used for analyzes