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Alliance With Therapeutic Entourage in Support of Young Suicidal (IPSI2)

C

Caen University Hospital

Status

Completed

Conditions

Suicide

Treatments

Other: Therapeutic alliance

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Enrollment

292 patients

Sex

All

Ages

13 to 40 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Supportive Care

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

292 participants in 1 patient group

Therapetic alliance
Other group
Treatment:
Other: Therapeutic alliance

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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