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OpenTrials
Completed

NCT Number: NCT02524535

Alliance With Therapeutic Entourage in Support of Young Suicidal

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.

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Key information

Age range

13 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

service de pédopsychiatrie, CHU de Caen

Caen, 14000, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Therapeutic alliance

Other

Primary outcomes

  1. characteristics of the mobilization of the entourage evaluated with Family Assessment Device

    Time frame: baseline

Sponsors and collaborators

Lead sponsor

University Hospital, Caen

Other

Registry information

Acronym: IPSI2

Important dates

Study start
2007
Primary completion
2013
First posted
Aug 14, 2015
Registry last updated
Aug 14, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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