Alliance With Therapeutic Entourage in Support of Young Suicidal

Suicide Clinical Trial

— IPSI2  

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02524535
• Other study ID #: 06-088
• Status: Completed
• Phase: N/A
• First received: August 13, 2015
• Last updated: August 13, 2015
• Start date: April 2007

Study information

• Verified date: August 2015
• Source: University Hospital, Caen
• Contact: n/a
• Is FDA regulated: No
• Health authority: France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
• Study type: Interventional

Clinical Trial Summary

Regardless of age, the quality of hospital care, the confidence that the young can have in the health care team, joining parents are pivotal elements and influence followed. Family support is all the more important as 14% of young people realize a new suicidal act within three months of hospitalization for attempted suicide, and that the essential predictors appear to be the young age and quality of intra-family relationships.

The main objective of this study is to determine, through the construction of an instrument to quantify the therapeutic alliance, defined by the characteristics of the mobilization of the entourage and the mutual commitments in the care of nursing teams and the entourage, the role of early therapeutic alliance with the entourage of suicidal youth 13-40 years, whether primosuicidants or repeat offenders, on short and medium term recurrences and early mortality.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 292
• Est. primary completion date: January 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 13 Years to 40 Years

Eligibility

Inclusion Criteria:

• Patient aged 13-40 years

• From male or female

• Supported the waning of a suicidal gesture.

• speaking and writing fluent French

• living in Upper or Lower Normandy

• signed informed consent form, and at least one of his parents after oral and written information about the study for minors.

Exclusion Criteria:

• Age <13 years or > 40 years

• Do not live in the Upper and Lower Normandy regions

• Detained patient

• forced hospitalization

• Patient under guardianship

• Patient with severe somatic pathology (cancer, heart failure, kidney or respiratory, central neurological disorder), scalable, or likely to be life-threatening within a period of less than one year

• Refusal to participate in the study

• Inability to respond

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care

Related Conditions & MeSH terms

• Suicide

Intervention

Other:
• Therapeutic alliance

Locations

Country	Name	City	State
France	service de pédopsychiatrie, CHU de Caen	Caen

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Caen

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	characteristics of the mobilization of the entourage evaluated with Family Assessment Device		baseline	No