NCT05136989

Brief Summary

Psychiatric establishments show significant disparities in terms of coercion: while some use it frequently, others use it only exceptionally. This project aims at a better understanding of the less coercive establishments, which are currently little investigated and whose study may allow to identify the levers of a psychiatry more respectful of individual liberties.

Trial Health

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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
98

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Dec 2021

Typical duration for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 16, 2021

Completed
14 days until next milestone

First Posted

Study publicly available on registry

November 30, 2021

Completed
1 day until next milestone

Study Start

First participant enrolled

December 1, 2021

Completed
2.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 1, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 1, 2024

Completed
Last Updated

March 12, 2024

Status Verified

March 1, 2024

Enrollment Period

2.5 years

First QC Date

November 16, 2021

Last Update Submit

March 8, 2024

Conditions

Keywords

PsychiatryReduction of coercionInterviewsObservationsSociologyNursing

Outcome Measures

Primary Outcomes (1)

  • understand the history of less coercive institutions

    identify and characterize the presence of tools, knowledge, rules, organizational specificities and collaborations in the territories allowing for less recourse to coercion.

    Baseline from 24 months

Secondary Outcomes (4)

  • Analysis of professionals' satisfaction

    Baseline from 24 months

  • Analysis of ex-patients' satisfaction

    Baseline from 24 months

  • Analysis of the impact on care pathway

    Baseline from 24 months

  • Analysis of the impact on career paths

    Baseline from 24 months

Study Arms (2)

Professionals from the seven least coercive facilities

Volunteer professionals selected on the basis of their experience in reducing the use of coercion.

Behavioral: Individual and collective semi-structured interviewsBehavioral: Observations out in the services

Voluntary ex-patients

Voluntary ex-patients who were hospitalized in these establishments in the two years preceding the survey and whose condition is stabilized

Behavioral: Individual semi-structured interviews with ex-patients

Interventions

Individual and collective semi-structured interviews will be performed with professionals to identify levers (practices, knowledge, tools, regulations) which, at the level of services and establishments, enable the development of a policy of less recourse to coercion

Professionals from the seven least coercive facilities

Individual semi-structured interviews will be performed with ex-patients in order to gather their experiences in the seven institutions concerned and to better understand the impact of their hospitalization in these institutions on their lives

Voluntary ex-patients

Observations will be carried out in the services in order to measure the gap between rhetoric and practice, and to observe the effective implementation of lesser use practices

Professionals from the seven least coercive facilities

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The research focuses mainly on care and support professionals, administrative and management staff, and users of seven establishments or poles identified as less coercive (three establishments in the Auvergne-Rhône-Alpes region, and four establishments on the national territory).

You may qualify if:

  • Professionals who worked in one of the seven establishments identified
  • Ex-patients who were hospitalized in these establishments in the two years preceding the survey and whose condition is stabilized

You may not qualify if:

  • People who refused to participate to the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CHU Saint Etienne

Saint-Etienne, 42000, France

RECRUITING

Study Officials

  • Sébastien SAETTA, PhD

    CHU de Saint-Etienne

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Study Design

Study Type
observational
Observational Model
ECOLOGIC OR COMMUNITY
Time Perspective
OTHER
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 16, 2021

First Posted

November 30, 2021

Study Start

December 1, 2021

Primary Completion

June 1, 2024

Study Completion

June 1, 2024

Last Updated

March 12, 2024

Record last verified: 2024-03

Locations