Clinical Trials Logo

Clinical Trial Summary

Losing contact with adult suicide attempters in the year after the suicide attempt (SA) increases the risk of recurrence. The situation with adolescents is unknown. Investigators aimed to determine whether being lost to contact early (LCE) by clinicians is a risk factor of longterm SA recurrence among adolescents and the associated factors.


Clinical Trial Description

Local clinical practice :

After an SA, adolescents receive treatment in the Children's Hospital or in the center of psychiatric consultation (few go to a private care clinic). All centers of psychiatric consultation belong to the same hospital center, which uses a unique medical record. According to the local clinical practice, patients and their parents systematically meet the child and adolescent psychiatric-department social worker at the time of the SA. The social worker informs the family that they will be called after 1 year to determine whether patients are safe or whether they need to resume care. For this call, the social worker uses the phone number listed in the medical record or finds the phone number in the national phone directory. If the social worker fails to contact the patient, the patient is considered LCE.

Patient follow-up :

Ten years after the index SA (every other year from 2004 to 2010), a self-reporting questionnaire will be sent to all adolescent suicide attempters and their parents, with a letter explaining the research. If the address of the patient is not available, the hospital records department will be contacted to collect these data for patients who will be re-hospitalized during the study period. When adolescent suicide attempters will be not contacted and when no information will be found in hospital records, the French Civil status Office will be called to determine whether patients were still alive. When no further information will be obtained, the adolescent will be considered lost to follow-up (LF) at the time of the last information from 1 to 10 years after the index SA.

Data collection :

At the time of the index SA, personal and family data will be collected from medical records for adolescents: personal characteristics (sex, age, history of SA [yes/no], psychiatric comorbidities of the SA [yes/no] according to the International Classification of Disease 10 (WHO, 1993), school difficulties [yes/no], and family characteristics (marital relationship of parents [separated or not], professional status of each parent [working or not], family history of SA [yes/no], and alcoholic dependence of parents [yes/no]). After the index SA, data on duration of hospitalization, psychiatric follow-up [yes/no], recurrence of SA in the year following the index SA (early SA recurrence [yes/no]), and LCE status [yes/no]) will be collected. Ten years after the index SA, a self-reporting questionnaire will be sent to the patient to assess SA recurrence. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02887170
Study type Observational
Source Central Hospital, Nancy, France
Contact
Status Completed
Phase
Start date January 1994
Completion date December 2010

See also
  Status Clinical Trial Phase
Recruiting NCT05848089 - Real-time Intervention for Suicide Risk Reduction N/A
Not yet recruiting NCT04686162 - Bae: A Smartphone Application for a Better Following Adolescents at Risk of Suicidal Behavior: Study of Acceptability and Preliminary Results of Efficacy N/A
Completed NCT04026308 - Written vs Electronic Safety Planning Study N/A
Recruiting NCT04770168 - Harry Potter as a Novel Educational Paradigm to Improve Mental Wellness in Children: A Prospective Trial N/A
Completed NCT03427190 - Suicide Prevention Algorithm in the French Overseas Territories N/A
Recruiting NCT05996172 - Swift Outpatient Alternatives for Rapid Stabilization N/A
Not yet recruiting NCT06378541 - Smartphone App Enhanced Facilitation Among Veterans in a Mental Health Inpatient Setting (Project HOPE) N/A
Recruiting NCT03026387 - Evaluation of the Risk Associated With Impulsivity and Other Neuropsychological Factors on Suicidal Relapse Within Hospital Emergencies N/A
Recruiting NCT04585802 - Expansion and Reevaluation of the Implicit Association Test in Suicide Ideators and Suicide Attempters
Completed NCT01398891 - Development of a Positive Psychology Intervention to Reduce Suicide Risk N/A
Completed NCT00735540 - Clinical Diagnosis of Teenagers Admitted to Pediatric Departments N/A
Completed NCT01502436 - An Exploration of the Relationship Between Chronic Pain and Suicide Attempt Among Veterans
Completed NCT00736918 - RCT of Post-Suicide Attempt Case Management (ACTION-J) Phase 3
Completed NCT02414763 - Pilot Study of a Brief Intervention for Medically Hospitalized Suicide Attempt Survivors Phase 1
Completed NCT02505373 - ASSIP, Attempted Suicide Short Intervention Program. Two Year Follow-Up Study N/A
Recruiting NCT06233747 - Improving Care, Accelerating Recovery and Education N/A
Recruiting NCT06223867 - Efficacy, Effectiveness, and Implementation of Jaspr Health in Emergency Department- Part A N/A
Completed NCT05158946 - A Future-oriented Group Training for Suicidal Patients N/A
Recruiting NCT05955807 - Momentary Assessment.Tracking Suicidal Ideation
Recruiting NCT05707975 - Eco-anxiety and Suicide