Cross-over Study of Three Modular Devices for Aid in Patient Standing and Transfer (VTT)
25 mars 2015 mis à jour par: Centre Hospitalier Universitaire de Nīmes
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".
Aperçu de l'étude
Statut
Complété
Les conditions
Description détaillée
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).
Type d'étude
Interventionnel
Inscription (Réel)
30
Phase
- N'est pas applicable
Contacts et emplacements
Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.
Lieux d'étude
-
-
-
Nîmes Cedex 09, France, 30029
- CHU de Nîmes - Hopital Universitaire Caremeau
-
-
Critères de participation
Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.
Critère d'éligibilité
Âges éligibles pour étudier
75 ans et plus (Adulte plus âgé)
Accepte les volontaires sains
Non
Sexes éligibles pour l'étude
Tout
La description
Inclusion Criteria:
- The patient must have given his/her informed and signed consent
- The patient must be insured or beneficiary of a health insurance plan
- The patient is in stable medical condition (no complications in the last 10 days)
- The patient is unable to stand up by his/her self and requires help during transfers
- The patient has muscular force (quadriceps) > 3 out of 5.
Exclusion Criteria:
- The patient is participating in another study
- The patient is in an exclusion period determined by a previous study
- The patient is under judicial protection, under tutorship or curatorship
- The patient refuses to sign the consent
- It is impossible to correctly inform the patient
- The patient is pregnant, parturient, or breastfeeding
- The patient has a limited support from at least one lower limb
- The patient has an unstable fracture
- The patient has a fragile heart
- The patient has joint pain localized in the knee, hip or ankle.
- The patient has already used one of three mechanisms to help with standing and transfer used in this study
- Behavioral problems (opposition, agitation)
Plan d'étude
Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Soins de soutien
- Répartition: Randomisé
- Modèle interventionnel: Affectation croisée
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: Turner-Vertic'Easy-Tina
Standing will be attempted with the three devices in the following order: (1) Turner; (2) Vertic'Easy; (3) Tina.
|
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.
Autres noms:
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
Autres noms:
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
Autres noms:
|
|
Expérimental: Turner-Tina-Vertic'Easy
Standing will be attempted with the three devices in the following order: (1) Turner; (2) Tina; (3) Vertic'Easy.
|
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.
Autres noms:
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
Autres noms:
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
Autres noms:
|
|
Expérimental: Vertic'Easy-Turner-Tina
Standing will be attempted with the three devices in the following order: (1) Vertic'Easy; (2) Turner; (3) Tina.
|
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.
Autres noms:
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
Autres noms:
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
Autres noms:
|
|
Expérimental: Vertic'Easy-Tina-Turner
Standing will be attempted with the three devices in the following order: (1) Vertic'Easy; (2) Tina; (3) Turner.
|
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.
Autres noms:
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
Autres noms:
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
Autres noms:
|
|
Expérimental: Tina-Turner-Vertic'Easy
Standing will be attempted with the three devices in the following order: (1) Tina; (2) Turner; (3) Vertic'Easy.
|
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.
Autres noms:
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
Autres noms:
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
Autres noms:
|
|
Expérimental: Tina-Vertic'Easy-Turner
Standing will be attempted with the three devices in the following order: (1) Tina; (2) Vertic'Easy; (3) Turner.
|
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.
Autres noms:
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
Autres noms:
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
Autres noms:
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Level of forward flexion of the spine (position of maximum horizontal displacement of C7)
Délai: Baseline (Day 0; cross-sectional study)
|
cm
|
Baseline (Day 0; cross-sectional study)
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Level of standing (maximum vertical displacement C7)
Délai: Baseline (Day 0; transversal study)
|
cm
|
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)
Délai: Baseline (Day 0; transversal study)
|
degrees
|
Baseline (Day 0; transversal study)
|
|
Standing time (time from start of forward flexion and the beginning of the vertical stabilization phase)
Délai: Baseline (Day 0; transversal study)
|
seconds
|
Baseline (Day 0; transversal study)
|
|
Verticalization achieved (yes/no)
Délai: Baseline (Day 0; transversal study)
|
yes/no
|
Baseline (Day 0; transversal study)
|
Collaborateurs et enquêteurs
C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.
Dates d'enregistrement des études
Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.
Dates principales de l'étude
Début de l'étude
1 septembre 2012
Achèvement primaire (Réel)
1 novembre 2012
Achèvement de l'étude (Réel)
1 novembre 2012
Dates d'inscription aux études
Première soumission
17 juillet 2012
Première soumission répondant aux critères de contrôle qualité
23 juillet 2012
Première publication (Estimation)
24 juillet 2012
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
26 mars 2015
Dernière mise à jour soumise répondant aux critères de contrôle qualité
25 mars 2015
Dernière vérification
1 mars 2015
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- LOCAL/2012/EV-03
- 2012-A00638-35 (Autre identifiant: RCB number)
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