Polypathology Clinical Trial
— LICORNEOfficial title:
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
| Verified date | September 2017 |
| Source | Centre Hospitalier Universitaire de Nice |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Observational |
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.
| Status | Completed |
| Enrollment | 57 |
| Est. completion date | January 5, 2017 |
| Est. primary completion date | January 5, 2017 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 60 Years to 100 Years |
| Eligibility |
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. |
| Country | Name | City | State |
|---|---|---|---|
| France | CHU de Nice | Nice |
| Lead Sponsor | Collaborator |
|---|---|
| Centre Hospitalier Universitaire de Nice |
France,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Improvment of the coordinnation around the patient defined by a change of at least one point on a 6 points Likert scale | 6 months | ||
| Secondary | Increase of the number of DMP for the patient using the plateform. Decrease of early hospital readmission | > 15 days | ||
| Secondary | Increase of the number of DMP for the patient using the plateform. Decrease of late hospital readmission | 1 month | ||
| Secondary | Decrease of the time ration hospital/home during the 6 month experimentation | 6 months |
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Not yet recruiting |
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