Clinical and Actigraphic Profile of Young Patients Admitted for Attempted Suicide

Not Applicable

Terminated

• Conditions: Suicide, Attempted
• Interventions: Behavioral: questionnaires; Device: actigraphic recording

• Registration Number: NCT02803632
• Lead Sponsor: Centre Hospitalier Universitaire, Amiens

Brief Summary

An excess suicide-related morbidity is observed among young people in the Picardie region, as reflected by the \> 100% occupation rate of the Amiens University Hospital Adolescent Medicine Unit

Detailed Description

An excess suicide-related morbidity is observed among young people in the Picardie region, as reflected by the \> 100% occupation rate of the Amiens University Hospital Adolescent Medicine Unit. New approaches have been proposed to these problems that have led us to reorganize our diagnostic practices: 1) more precise characterization of suicidal behaviour by using standardized instruments such as the French version of the Columbia-Suicide Severity Rating Scale developed by Posner (C-SSRS); 2) new clinical entities, such as disruptive mood dysregulation disorder, are now proposed in international classifications (DSM 5 field trial); 3) investigations such as recording of the circadian rhythm of motor activity by actigraphy are being studied as a laboratory complement to psychiatric diagnosis.

Study Timeline

• Study Start: 2013-02-06
• Study First Submitted: 2016-06-09
• Study First Submitted QC: 2016-06-14
• Study First Posted: 2016-06-17
• Primary Completion: 2018-08-24
• Study Completion: 2018-08-24
• Status Verified: 2020-12
• Last Update Submitted: 2020-12-04
• Last Update Posted: 2020-12-08

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 98

Inclusion Criteria

• children/adolescents admitted after a suicide attempt

Exclusion Criteria

• severe depression
• mental retardation
• pervasive developmental disorder
• active psychotic episode,
• drug and alcohol abuse at the time of admission
• organic sleep-wake disorders (sleep-related respiratory and motor disorders, narcolepsy)
• any contraindication formulated by the clinical team
• patients not covered by French national health insurance, patients deprived of their freedom as stipulated in Article L.1121-6 of the French Public Health Code

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
suicide attempt	questionnaires	questionnaires actigraphic recording
suicide attempt	actigraphic recording	questionnaires actigraphic recording

Primary Outcome Measures

Name	Time	Method
The variable absence / presence of the disruptive mood dysregulation disorder (DMDD)	Day 0	The variable absence / presence of the disruptive mood dysregulation disorder (DMDD)

Trial Locations

Locations (2)

AP HP; 🇫🇷 Paris, France

CHU Amiens; 🇫🇷 Amiens, France