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NCT Number: NCT06677645

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

Prospective, observational, non-interventional, comparative, multicenter RIPH3 study to investigate the impact of HTSH on length of hospital stay in referring services.

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Key information

Age range

60 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

CHU Bicêtre, Paris, Île-de-France Region, France

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About this study

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).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

  • Inclusion Criteria:
  • Patient selection 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.
  • 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.
  • 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.
  • Non-inclusion Criteria:
  • 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.

Treatment and study plan

Primary outcomes

  1. Study to investigate the impact of HTSH on length of hospital stay in referring services

    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.

Secondary outcomes

  1. Analysis of pathways and plans for returning home

    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.

  2. Analysis of HTSH patient profiles a) Proportion of eligible patients and their comorbidities b) Social profile + main reason for hospitalization of patients admitted to HTSH

    Time frame: 24 months

    Evaluation criteria:

    Ratio of hospital ward activity data to pre-screening data collected during the study.

  3. Analysis of discharges and patient outcomes

    Time frame: 24 months

    Proportion of patients remaining at home in the medium term Patients' functional outcome after the trial

  4. Quality of life and caregiver benefit analysis

    Time frame: 24 months

    Quality of life assessment

Study contacts

Contact information is provided by the study sponsor or research team.

Albatoul ZAKARIA, PhD

CONTACT

[email protected]

33 (0)185 781010

ISABELLE DUFOUR

CONTACT

[email protected]

33 (0) 185781011

Sponsors and collaborators

Lead sponsor

Gérond'if

Other

Registry information

Acronym: HTSH

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Nov 7, 2024
Registry last updated
Jun 13, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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