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.
Studieoversikt
Status
Intervensjon / Behandling
Studietype
Registrering (Forventet)
Kontakter og plasseringer
Studiesteder
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Nantes, Frankrike, 44093
- Rekruttering
- Nantes UH
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Ta kontakt med:
- Gilles Berrut
- E-post: gilles.berrut@chu-nantes.fr
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Ta kontakt med:
- Dibon Christelle
- E-post: christelle.dibon@chu-nantes.fr
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Prøvetakingsmetode
Studiepopulasjon
Beskrivelse
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)
Studieplan
Hvordan er studiet utformet?
Designdetaljer
Kohorter og intervensjoner
Gruppe / Kohort |
Intervensjon / Behandling |
|---|---|
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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
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Patients in complex situation taken care by classic plan
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Cost-utility analysis (CUA)
Tidsramme: 6 months
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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.
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6 months
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Samarbeidspartnere og etterforskere
Sponsor
Studierekorddatoer
Studer hoveddatoer
Studiestart
Primær fullføring (Forventet)
Studiet fullført (Forventet)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Andre studie-ID-numre
- RC14_0343
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