- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning 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.
Studieöversikt
Status
Betingelser
Detaljerad beskrivning
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.
Studietyp
Inskrivning (Faktisk)
Kontakter och platser
Studieorter
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Nice, Frankrike, 06000
- Chu De Nice
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Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Testmetod
Studera befolkning
Beskrivning
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.
Studieplan
Hur är studien utformad?
Designdetaljer
- Observationsmodeller: Kohort
- Tidsperspektiv: Blivande
Kohorter och interventioner
Grupp / Kohort |
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Kontrollera
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LICORNE platform
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Tidsram |
|---|---|
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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
Tidsram: 6 months
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6 months
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Sekundära resultatmått
Resultatmått |
Tidsram |
|---|---|
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Increase of the number of DMP for the patient using the plateform. Decrease of early hospital readmission
Tidsram: > 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
Tidsram: 1 month
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1 month
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Decrease of the time ration hospital/home during the 6 month experimentation
Tidsram: 6 months
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6 months
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Samarbetspartners och utredare
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Uppskatta)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Andra studie-ID-nummer
- 14-PP-17
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