NCT02809417

Brief Summary

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
57

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Jan 2016

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 28, 2016

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

June 20, 2016

Completed
2 days until next milestone

First Posted

Study publicly available on registry

June 22, 2016

Completed
7 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 5, 2017

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 5, 2017

Completed
Last Updated

September 25, 2017

Status Verified

September 1, 2017

Enrollment Period

11 months

First QC Date

June 20, 2016

Last Update Submit

September 22, 2017

Conditions

Outcome Measures

Primary Outcomes (1)

  • 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 Outcomes (3)

  • Increase of the number of DMP for the patient using the plateform. Decrease of early hospital readmission

    > 15 days

  • Increase of the number of DMP for the patient using the plateform. Decrease of late hospital readmission

    1 month

  • Decrease of the time ration hospital/home during the 6 month experimentation

    6 months

Study Arms (2)

LICORNE platform

Control

Eligibility Criteria

Age60 Years - 100 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

old patient with polypathologies and loss of autonomy

You may qualify if:

  • 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)

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CHU de Nice

Nice, 06000, France

Location

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 20, 2016

First Posted

June 22, 2016

Study Start

January 28, 2016

Primary Completion

January 5, 2017

Study Completion

January 5, 2017

Last Updated

September 25, 2017

Record last verified: 2017-09

Locations