Actively Recruiting
Evaluation of Medical and Social Care for Elderly Patients Between Hospital and Home Temporary Accommodation in Nursing Home and Long-Term Care Units in Ile-de-France Region
Led by Gérond'if · Updated on 2025-06-13
258
Participants Needed
10
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are evaluating the impact of a temporary accommodation program called HTSH on elderly patients' length of stay in hospital services. This observational, multicenter study involves elderly patients discharged from hospitals in the Ile-de-France region who require short-term accommodation in nursing homes or long-term care units. The study aims to assess how this program supports medical and social care and influences decisions about returning home after hospitalization. The study includes a prospective group of 258 subjects and a retrospective group using data from 2021 and 2022. Temporary accommodation beds are provided in dedicated units with specialized staff, physically grouped within establishments supported by the Regional Health Agency. The study compares hospital stay lengths before and after the program's implementation to evaluate its efficiency. Participants will be observed over 24 months with data collected on hospital stay length, patient pathways, profiles, discharge outcomes, quality of life, and caregiver benefits. Medical records and social evaluations are reviewed, and caregivers and professionals involved in the HTSH circuit may also participate. This non-interventional study monitors outcomes without changing usual care, with no specified maximum age and no healthy volunteers included.
CONDITIONS
Brief Title
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
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient male or female at least 60 years of age, 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
- Social or medical situation stabilized but does not allow immediate return home after hospitalization
- Person with unpaid caregiving activity for their relative in HTSH, able to understand and answer study questionnaires without help
- Salaried professional involved directly in the HTSH circuit for at least 6 months, with oral non opposition to participation documented
You will not qualify if you...
- Already included in another clinical study
- Under legal protection measures or unable to express consent according to French Public Health Code article L1121-8
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 24 months
Participants who undergo routine care in temporary accommodation between hospital and home are observed to evaluate their medical and social care and the decision to return home.
Assessments as per routine care during temporary accommodation
Trial Site Locations
Total: 10 locations
1
Résidence ZEMGOR
Cormeilles-en-Parisis, France, 95240
Not Yet Recruiting
2
EHPAD Pierre TABANOU
L'Haÿ-les-Roses, France, 94240
Actively Recruiting
3
Groupe Hospitalier Sud Ile de France (GHSIF)
Melun, France, 77000
Not Yet Recruiting
4
GHU Lariboisière
Paris, France, 75010
Not Yet Recruiting
5
Broca Hospital
Paris, France, 75013
Actively Recruiting
6
USDL Vaugirard, APHP
Paris, France, 75015
Actively Recruiting
7
Centre Hospitalier de Rambouillet
Rambouillet, France, 78514
Not Yet Recruiting
8
Centre Hospitalier de Versailles
Versailles, France, 78157
Active, Not Recruiting
9
Hopital Paul Brousse
Villejuif, France, 94800
Not Yet Recruiting
10
CHU Bicêtre
Paris, Île-de-France Region, France, 94270
Actively Recruiting
Research Team
I
ISABELLE DUFOUR
A
Albatoul ZAKARIA, PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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