NCT02348892

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.

Trial Health

43
At Risk

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Dec 2014

Geographic Reach
1 country

1 active site

Status
unknown

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

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 1, 2014

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

January 16, 2015

Completed
12 days until next milestone

First Posted

Study publicly available on registry

January 28, 2015

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

February 1, 2016

Completed
Last Updated

January 28, 2015

Status Verified

January 1, 2015

Enrollment Period

1.2 years

First QC Date

January 16, 2015

Last Update Submit

January 22, 2015

Conditions

Outcome Measures

Primary Outcomes (1)

  • Cost-utility analysis (CUA)

    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.

    6 months

Study Arms (2)

With coordinator

Elderly patients, in complex situation, taken care by coordinator

Other: Coordinator

Without coordinator

Elderly patients, in complex situation, taken care by the classic plan

Other: Classic plan

Interventions

Patients in complex situation taken care by coordinator

With coordinator

Patients in complex situation taken care by classic plan

Without coordinator

Eligibility Criteria

Age70 Years+
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)
Sampling MethodProbability Sample
Study Population

The eligible patients for the study will be the patients of 70 and more years old hospitalized in the Nantes UH in the acute care medical department internal medical departement medical urgency, rehabilitation unit, neurology, gastro-enterology of the CHU of Nantes and which are in complex medical and social situation, whoever is their motive for hospitalization.

You may qualify if:

  • 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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Nantes UH

Nantes, 44093, France

RECRUITING

Study Design

Study Type
observational
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 16, 2015

First Posted

January 28, 2015

Study Start

December 1, 2014

Primary Completion

February 1, 2016

Study Completion

February 1, 2016

Last Updated

January 28, 2015

Record last verified: 2015-01

Locations