Outpatient Nurse Monitoring Under the Prevention of Recurrent Suicidal

Mood Disorder Clinical Trial

— SIPRéS  

Official title:

Randomized Study of Ambulatory Monitoring Nurse Under the Prevention of Recurrent Suicidal

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02721316
• Other study ID #: UF9533
• Status: Completed
• Phase: N/A
• Start date: May 2016
• Est. completion date: October 2021

Study information

• Verified date: February 2022
• Source: University Hospital, Montpellier
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

To evaluate the impact of a specific nursing management (personalized and close, through consultation at the hospital, at home or by phone) monitoring in post-hospitalization, the suicide attempt of recurrence and suicidal crisis, in the year following a suicide attempt in patients suffering from a mood disorder (unipolar or bipolar) or reactive depression.

Description:

Main objective: To evaluate the impact of a specific nursing management (personalized and close, through consultation at the hospital, at home or by phone) monitoring in post-hospitalization, the suicide attempt of recurrence and suicidal crisis, in the year following a suicide attempt in patients suffering from a mood disorder (unipolar or bipolar) or reactive depression. Secondary objectives: Studying during the year following the suicide attempt index, the impact of this device on: - The frequency and intensity of suicidal ideation - the spontaneous use of emergency care - the death rate from suicide and other causes - the cumulative duration of hospitalization for suicidal behavior - The patient's quality of life - the number of patients lost to at the end of search Studying patient compliance with intensive nursing monitoring program. To study the role of the nurse to determine the factors that promote the construction of a therapeutic alliance. Establish a mapping of needs and resources suicidal patient for nursing care in post-emergency.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 380
• Est. completion date: October 2021
• Est. primary completion date: May 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 90 Years

Eligibility

Inclusion Criteria:

• Patient suffering from a mood disorder (unipolar or bipolar) or reactive depression whose reason for hospitalization in the Psychiatric Emergency Unit Post has attempted suicide

Exclusion Criteria:

• Patients with bipolar disorder, current episode manic in
• Patient Hospitalized full-time (for high suicide risk incompatible with an output of emergencies or clinical transfer) within 3-5 days of the TS
• Patient suffering from a somatic pathology associated with the prognosis is committed in the short term.
• Patients suffering from a neurodegenerative pathology of dementia or pre-dementia types.
• Homeless Patient

Related Conditions & MeSH terms

• Adjustment Disorders
• Mood Disorder
• Mood Disorders
• Reactive Depression

Intervention

Other:
• Supported with intensive nursing follow post hospitalization
Intensive nursing follow post - hospitalization

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Montpellier

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change the suicidal rate of recurrence between patients with intensive nursing follow post - hospitalization and patients with usual care		Day 3rd, 6rd day, 3 weeks, 6 weeks and 12 week after emergency exit
Secondary	Change in the number of emergency hospitalization for suicidal crisis without acting out between patients with intensive nursing follow post - hospitalization and patients with usual care		Day 3rd, 6rd day, 3 weeks, 6 weeks and 12 week after emergency exit