Actively Recruiting

Age: 18Years - 65Years
All Genders
NCT06250296

Evaluation of a New Recovery-oriented Model of Psychiatric Inpatient Care

Led by University Hospital, Geneva · Updated on 2024-07-03

700

Participants Needed

1

Research Sites

84 weeks

Total Duration

On this page

Sponsors

U

University Hospital, Geneva

Lead Sponsor

F

Fondation Privée des HUG

Collaborating Sponsor

AI-Summary

What this Trial Is About

This project will study the effects of a major reorganization of psychiatric inpatient wards. This reorganization will affect many aspects of day-to-day work, with the aim of improving the individualization of care, the integration of relatives and the participation of the patients in treatment planning. This new organization will initially involve a first pilot ward, before being extended to other wards. The aim of this project is to understand whether this new organization has positive effects on the use of coercive measures, the average length of stay, the improvement in patients' clinical condition, as well as on patient satisfaction, their perception of coercion, the wards' atmosphere on the unit and patients' personal recovery. All patients admitted to three wards of the Division of adult psychiatry of the Geneva University Hospital aged 18 and over, with a good knowledge of French and being treated for any type of diagnosis except dementia, are invited to take part in the study. They will be assessed at discharge regarding the selected outcomes. The study will last 18 months: during the first 9 months, the new model will be applied on the pilot ward, and the wo other wards will serve as comparison wards. After 9 months, the model will also be applied to these other two wards.

CONDITIONS

Official Title

Evaluation of a New Recovery-oriented Model of Psychiatric Inpatient Care

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients hospitalized in one of the three participating wards
Not Eligible

You will not qualify if you...

  • Incapacity to give informed consent
  • Insufficient knowledge of French

AI-Screening

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Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

HUG - Hôpital de Belle-Idée

Thônex, Switzerland, 1226

Actively Recruiting

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Research Team

A

Alexandre Wullschleger, MD

CONTACT

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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