Impact of Joint Crisis Plan

NCT ID: NCT03984682

Last Updated: 2024-04-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

96 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-11-21

Study Completion Date

2024-04-04

Brief Summary

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For some patients in department psychiatric, isolation measures are put in place. But the measures is not pleasant for the patient or for the care team.

That's why care team are trying to find ways to improve patient care, including asking them how they would like to be treated.

One of the solutions is called the Joint Crisis Plan. A Joint Crisis Plan is a personalized procedure for a patient. It describes the attitude, the care, the measures in case of crisis with the patient and his family. Patients indicate their wishes regarding their care. However, there is no real scientific proof of the effectiveness of this Joint Crisis Plan, especially to reduce isolation measures.

Detailed Description

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The primary objective of this study is to evaluate efficacy of the Joint Crisis Plan.

Conditions

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Mental Disorders

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

OTHER

Blinding Strategy

NONE

Study Groups

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Experimental group

Patients will benefit from regular care + Joint Crisis Plan

Group Type EXPERIMENTAL

Joint Crisis Plan

Intervention Type PROCEDURE

A Joint Crisis Plan will be drafted with the patient and a nurse

Control group

Patients will benefit from regular care

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Joint Crisis Plan

A Joint Crisis Plan will be drafted with the patient and a nurse

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patients \>18 years
* Patients having had at least one isolation, restraint or forced hospitalization measure in the 24 months before inclusion
* Followed by nurses of a mobile team of psychiatry sector Saint Etienne
* Social security affiliation
* Signed informed consent

Exclusion Criteria

* Patient having already had a Joint Crisis Plan for less than 6 months.
* Patient does not speak French
* Pregnant and lactating women
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Ministry of Health, France

OTHER_GOV

Sponsor Role collaborator

Centre Hospitalier Universitaire de Saint Etienne

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Yvonne QUENUM, Coordinating nurse

Role: PRINCIPAL_INVESTIGATOR

CHU SAINT-ETIENNE

Locations

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CHU Saint-Etienne

Saint-Etienne, , France

Site Status

Countries

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France

Other Identifiers

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ANSM

Identifier Type: OTHER

Identifier Source: secondary_id

18PH221

Identifier Type: -

Identifier Source: org_study_id

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