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Clinical Trials/NCT02348892
NCT02348892
Unknown
N/A

Evaluation Program of the Benefit of the Coordination of the Course of the Elderly Patient in Health Establishment - Pilot Study.

Nantes University Hospital1 site in 1 country100 target enrollmentDecember 2014

Overview

Phase
N/A
Intervention
Not specified
Conditions
Elderly Patients in Complex Situations
Sponsor
Nantes University Hospital
Enrollment
100
Locations
1
Primary Endpoint
Cost-utility analysis (CUA)
Last Updated
11 years ago

Overview

Brief Summary

The large share of chronic diseases correlated with an aging population calls to develop necessary coordination between the hospital and non-hospital (professional of the city, home ...) to create new complementarities.

Since July 2013, the Nantes University Hospital experiences the establishment of a coordinator route patient in Gerontology. The evaluation program of the benefit of coordinating the course in elderly patients in health establishment (PROCOPES) must allow to prove the efficiency of the intervention of a coordinator route patient, following elderly patients in complex situations, both within the hospital and outside the hospital (home, nursing home,...). The objective of PROCOPES is to show the added value of an innovative position that can make the link between the hospital and the city on deemed complex situations.The pilot study results present a strong interest for health care settings, nursing home and in the world of research. It will also permit to have preliminary data for bigest studies.

Registry
clinicaltrials.gov
Start Date
December 2014
End Date
February 2016
Last Updated
11 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patient of 70 and more years old
  • Patient living on Nantes
  • Hospitalized in Nantes UH
  • Patient whose the hospitalization is not relevant at the time of the request of trajectory case manager
  • Patient whose the situation is complex (without solution at the time of the request)
  • Patient (or legal representative) having given his assent of participation

Exclusion Criteria

  • Patient (or legal representative) refusing to participate in the protocol
  • Patient whose follow-up is impossible (ex: programmed move, life expectation)

Outcomes

Primary Outcomes

Cost-utility analysis (CUA)

Time Frame: 6 months

A differential cost-utility ratio will be used to compare both interventions. The evaluation of costs will take into account direct health care insurance cost, hospital costs and patient cost (according to the french health care insurance system). The evaluation of utility will be based on the evaluation of patient's quality of life, measured by EuroQol EQ-5D.

Study Sites (1)

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