- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT02098655
Analysis of the Parameters Obtained on Stabilometric Platform in Patients With PD (SPPD001)
Analysis of the Parameters Obtained on Stabilometric Platform in Patients With Parkinson's Disease: a Basis for a Rehabilitation Perspective
Aperçu de l'étude
Statut
Intervention / Traitement
Description détaillée
Background: Posture and balance are the foundation on wich upright stance and walking are executed. Postural instability is the impairment in balance that compromises the ability to maintain or change posture such as standing and walking. It is considered to be one of the cardinal features of PD. In such patients it is present even at diagnosis and worsens with disease progression. It correlates with falls representing a major source of disability and reduced QoL in PD. In this course, the study of balance is important to identify patients who can benefit from specific rehabilitative treatment.
Objective: To analyze different parameters in patients with PD obtained through the use of a stabilometric platform and compare them with those of a control population. To interpret the data in order to find some postural instability indicators that can become useful to build a rehabilitation strategy for balance disorders in PD.
Type d'étude
Inscription (Anticipé)
Contacts et emplacements
Lieux d'étude
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-
Como
-
Gravedona, Como, Italie, 22015
- Recrutement
- Ospedale Generale di Zona "Moriggia-Pelascini"
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Contact:
- Giuseppe Frazzitta, MD
- Numéro de téléphone: +39034492552
- E-mail: frazzittag62@gmail.com
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Chercheur principal:
- Giuseppe Frazzitta, MD
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-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
Méthode d'échantillonnage
Population étudiée
La description
Inclusion Criteria:
- PD according to Gelb et al., in Hoehn-Yahr stage 3, with the ability to walk without any assistance, who had fallen in the last year at least 2 times, with mini-mental state examination score ≥26.
- Healthy volunteers
Exclusion Criteria:
- atypical parkinsonism
- patients with cerebro-vascular disorders or other neurological conditions including cognitive impairment.
- patients with relevant comorbidity or vestibular/visual dysfunctions limiting locomotion or balance.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
Cohortes et interventions
Groupe / Cohorte |
Intervention / Traitement |
---|---|
30 patients with PD
30 patients (12 M, 18 F, mean age 66,8 ± 8,7) with PD in stage 3 of H&Y will undergo training of balance using a stabilometric platform
|
Stabilometric platform is a device used for assessment and training of balance basing on ground reaction force evaluation in static conditions.
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12 healthy volunteers
12 healthy volunteers (3 M, 9 F, mean age 66,5 ± 6,0) served as controls will undergo training of balance using a stabilometric platform
|
Stabilometric platform is a device used for assessment and training of balance basing on ground reaction force evaluation in static conditions.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
Trunk sway
Délai: One week
|
With respect to the average centre of gravity the Standard Deviation of trunk sway (total, in Antero-Posterior and in Medio-Lateral direction) were calculated.
In this way it was possible to obtain a statokinesigram, that is the layout of a line connecting the successive positions of the center of pressure during the recording, and the area of the ellipse containing 90% of the sampled positions of the center of pressure.
These measurements were obtained with open eyes (OE), and while the patient performing a cognitive task (counting).
|
One week
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
BBS
Délai: One week
|
Berg Balance Scale
|
One week
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Collaborateurs et enquêteurs
Les enquêteurs
- Chercheur principal: Giuseppe Frazzitta, MD, Parkinson disease and movement disorders rehabilitation unit, Ospedale Generale di Zona "Moriggia-Pelascini", Gravedona ed Uniti (CO), Italy
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
Achèvement primaire (Anticipé)
Achèvement de l'étude (Anticipé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- SP PD 001 (Autre identifiant: Ospedale Generale di Zona Moriggia-Pelascini)
Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .
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