- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT02809417
Interest of the Use of the Web Platform LICORNE (LIaison and COoRdination With a NumériquE Health Reseau) Concerning Coordination of Care for Dependant Elderly Patients (LICORNE)
This project is associating partners from the public area (university hospital of Nice, Nice university) and the private area (Agfa Health Care, Radhuis, Domicalis) to create a unique medico-psycho-social shared record.
The purpose of this project is to significantly improve coordination of care, especially between hospital and home. We can expect a significant improvement in the patient's living conditions, improving its management, its security and ultimately, lower health care costs.
Aperçu de l'étude
Statut
Les conditions
Description détaillée
The LICORNE project was created to give the possibility for the medical establishments to share there medico-psycho-social informations with all actors taking part of the patient care. Indeed, current informatique systems in medical establishments have an isolated functionning, without transmission of information outsite the wall of the hospital. The idea of this project is to bring together all actors involved in the care of a patient around a single shared patient record, regardless of the structures where professionnals work. This project is associating partners from the public area (university hospital of Nice, Nice university) and the private area (Agfa Health Care, Radhuis, Domicalis) to create a unique medico-psycho-social shared record. The informations will be share between all the professionnal taking car of the patient.
The main objective of this protocol will be to determine the impact of using the LICORNE platform on the coordination of care of elderly patients with multiple diseases. We will assess the impact of using the LICORNE platform on the implementation of electronic health record (Dossier Médical Partagé, public health insurance of the social security), and the benefit of using the LICORNE platform to reduce patient's hospital readmissions.
The purpose of this project is to significantly improve coordination of care, especially between hospital and home. We can expect a significant improvement in the patient's living conditions, improving its management, its security and ultimately, lower health care costs.
Type d'étude
Inscription (Réel)
Contacts et emplacements
Lieux d'étude
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Nice, France, 06000
- Chu De Nice
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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:
- Age> 60 years
- multiple pathologies : having at least two active chronic conditions.
- Polypharmacy : having at least 4 different molecules in its treatment.
- Dependence : GIR 4 or equivalent and less before hospitalization.
- Need medical care at home at least 5 days a week .
- Patient requiring social intervention ( this criterion of judgment is left to the social worker in the patient's file)
Exclusion Criteria:
- Life threatening pathology during current hospitalization .
- Patients undergoing a hospitalization home service .
- Patients without administrative or judicial freedom if the authorization of the legal representative can not be collected.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Modèles d'observation: Cohorte
- Perspectives temporelles: Éventuel
Cohortes et interventions
Groupe / Cohorte |
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Contrôle
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LICORNE platform
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
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Improvment of the coordinnation around the patient defined by a change of at least one point on a 6 points Likert scale
Délai: 6 months
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6 months
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Mesures de résultats secondaires
Mesure des résultats |
Délai |
|---|---|
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Increase of the number of DMP for the patient using the plateform. Decrease of early hospital readmission
Délai: > 15 days
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> 15 days
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Increase of the number of DMP for the patient using the plateform. Decrease of late hospital readmission
Délai: 1 month
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1 month
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Decrease of the time ration hospital/home during the 6 month experimentation
Délai: 6 months
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6 months
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Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
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 (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Autres numéros d'identification d'étude
- 14-PP-17
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