- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02348892
Evaluation Program of the Benefit of the Coordination of the Course of the Elderly Patient in Health Establishment - Pilot Study. (PROCOPES)
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.
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
-
-
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Nantes, France, 44093
- Recruiting
- Nantes UH
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Contact:
- Gilles Berrut
- Email: gilles.berrut@chu-nantes.fr
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Contact:
- Dibon Christelle
- Email: christelle.dibon@chu-nantes.fr
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
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)
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
With coordinator
Elderly patients, in complex situation, taken care by coordinator
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Patients in complex situation taken care by coordinator
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Without coordinator
Elderly patients, in complex situation, taken care by the classic plan
|
Patients in complex situation taken care by classic plan
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
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.
|
6 months
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start
Primary Completion (Anticipated)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- RC14_0343
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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