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Clinical Trials/NCT02721316
NCT02721316
Completed
Not Applicable

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

University Hospital, Montpellier0 sites380 target enrollmentMay 2016

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Mood Disorder
Sponsor
University Hospital, Montpellier
Enrollment
380
Primary Endpoint
Change the suicidal rate of recurrence between patients with intensive nursing follow post - hospitalization and patients with usual care
Status
Completed
Last Updated
3 years ago

Overview

Brief 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.

Detailed 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.

Registry
clinicaltrials.gov
Start Date
May 2016
End Date
October 2021
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

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

Outcomes

Primary Outcomes

Change the suicidal rate of recurrence between patients with intensive nursing follow post - hospitalization and patients with usual care

Time Frame: Day 3rd, 6rd day, 3 weeks, 6 weeks and 12 week after emergency exit

Secondary Outcomes

  • 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)

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