Improving Outcomes in Social Services Through Routine Outcome Monitoring and Systematic Client Feedback
NCT07303608
Behavior, Chemically-Induced Disorders
Linköping, Sweden
View Trial DetailsNCT Number: NCT06677645
Prospective, observational, non-interventional, comparative, multicenter RIPH3 study to investigate the impact of HTSH on length of hospital stay in referring services.
Interested in participating?
Request Info60 year and older
All sexes
Observational
CHU Bicêtre, Paris, Île-de-France Region, France
This is a multi-center study involving many hospital departments temporary accommodation at the end of hospitalization in several Nursing home/long term care units in Ile de France region. The temporary accommodation program was designed for elderly people living at home to find an accommodation solution in nursing home to meet a short-term need. Temporary accommodation beds are deployed and perpetuated in the Île-de-France region by the Regional Health Agency, physically grouped together in establishments within units with dedicated staff. The resources allocated to these beds have been increased. The aim of the study is to demonstrate the efficiency of the HTSH circuit, for elderly patients leaving hospital, in their medical and social care and the decision or not to return home. This project is supported by Regional Health Agency (ARS-IDF).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Time frame: 24 months
The main assessment criterion is based on the average length of stay observed at the end of the study, compared with that of the previous two years, 2021 and 2022, in the referring services.
Time frame: 24 months
Evaluation criteria:
Calculation of the proportion of patients in the life project on admission to nursing home / long term care units and the return home at the end of the stay.
Time frame: 24 months
Evaluation criteria:
Ratio of hospital ward activity data to pre-screening data collected during the study.
Time frame: 24 months
Proportion of patients remaining at home in the medium term Patients' functional outcome after the trial
Time frame: 24 months
Quality of life assessment
Contact information is provided by the study sponsor or research team.
Albatoul ZAKARIA, PhD
CONTACT
ISABELLE DUFOUR
CONTACT
Gérond'if
Other
Acronym: HTSH
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