Evaluation of Medical and Social Care for Elderly Patients, Between Hospital and Home: TEMPORARY ACCOMMODATION Out of Hospitalization by Nursing Home and Long-Term Care Units in Ile-de-France Region
NCT ID: NCT06677645
Last Updated: 2025-06-13
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
258 participants
OBSERVATIONAL
2024-11-20
2027-11-20
Brief Summary
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Detailed Description
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Conditions
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Study Design
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OTHER
PROSPECTIVE
Study Groups
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Prospective group
258 subjects in the prospective group
No interventions assigned to this group
Retrospective group
Retrospective data will be collected directly from hospital departments by ARS IDF or from physicians responsible for medical information (RMI) within each hospital center participating in the study, for the 2 years 2021 and 2022 prior to the study and compared with the average length of stay for services to be calculated at the end of the study.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* Patient male or female at least 60 years of age, as initially defined with the Regional Health Agency, discharged from hospital,
* Oral expression of non opposition to participation in the study, documented in the medical record by the physician,
* Presenting a defined and feasible plan for returning home,
* Whose social/medical situation (stabilized) does not allow an immediate return home after hospitalization.
2. Caregiver selection criteria
* Person with an unpaid caregiving activity for their relative in HTSH,
* Person verbally expressing their non-opposition to participating in the study, and documented in the medical record of the patient they are helping,
* A person who is able to understand the study questionnaires and evaluations, and is able to answer them without the help of a third party.
3. Professional selection criteria
* Salaried professional, nursing or not, regularly and directly involved in the HTSH circuit, whether in hospital or in nursing home / long term care units, for at least 6 months,
* Oral expression of non opposition to participation in the study, documented by the establishment.
* Be already included in another clinical study,
* Benefit from a legal protection measure or be unable to express their consent, in accordance with article L1121-8 of the French Public Health Code.
60 Years
ALL
No
Sponsors
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Gérond'if
OTHER
Responsible Party
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Locations
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Résidence ZEMGOR
Cormeilles-en-Parisis, , France
EHPAD Pierre TABANOU
L'Haÿ-les-Roses, , France
Groupe Hospitalier Sud Ile de France (GHSIF)
Melun, , France
GHU Lariboisière
Paris, , France
Broca Hospital
Paris, , France
USDL Vaugirard, APHP
Paris, , France
Centre Hospitalier de Rambouillet
Rambouillet, , France
Centre Hospitalier de Versailles
Versailles, , France
Hopital Paul Brousse
Villejuif, , France
CHU Bicêtre
Paris, Île-de-France Region, France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2024-A00023-44
Identifier Type: -
Identifier Source: org_study_id
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