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NCT02803632 Clinical Trial

Clinical and Actigraphic Profile of Young Patients Admitted for Attempted Suicide

Suicide, Attempted Clinical Trial

— ACTIHUMEUR  

Official title:
Clinical and Actigraphic Profile of Young Patients Admitted for Attempted Suicide: Investigation of Disruptive Mood Dysregulation Disorder

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT02803632
Other study ID # AOL11-DR -GUILE
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date February 6, 2013
Est. completion date August 24, 2018

Study information
Verified date December 2020
Source Centre Hospitalier Universitaire, Amiens
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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

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.

Recruitment information / eligibility
Status Terminated
Enrollment 98
Est. completion date August 24, 2018
Est. primary completion date August 24, 2018
Accepts healthy volunteers No
Gender All
Age group 6 Years to 17 Years
Eligibility 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

Related Conditions & MeSH terms

Intervention

Behavioral:
• questionnaires

Device:
• actigraphic recording

Locations
Country Name City State
France CHU Amiens Amiens
France AP HP Paris

Sponsors (1)
Lead Sponsor Collaborator
Centre Hospitalier Universitaire, Amiens

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary The variable absence / presence of the disruptive mood dysregulation disorder (DMDD) The variable absence / presence of the disruptive mood dysregulation disorder (DMDD) Day 0
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