Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
246 participants
OBSERVATIONAL
1994-01-31
2010-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
ACCeptation and Qualitative Evaluation of Phone-delivered Intervention
NCT02949453
Suicide Re Attempts in Young Adults After First Suicide Attempt : Socio-demographic, Clinical and Biological Correlates
NCT03538197
Qualitative Assessment of the Brief Contact Intervention "Stay in Contact" in Suicide Prevention
NCT03325478
The Life Paths That Lead Teenagers to Attempted Suicide:Trajectories of Proximal Adversity
NCT04638205
Effect of Telephone Follow-up on Repeated Suicide Attempt in Patients
NCT02932709
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
RETROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
13 Years
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Central Hospital, Nancy, France
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
GUILLEMIN Francis, MD
Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Fabienne LIGIER
Role: PRINCIPAL_INVESTIGATOR
Nancy University Children's Hospital
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
CHRU Nancy
Nancy, , France
Countries
Review the countries where the study has at least one active or historical site.
References
Explore related publications, articles, or registry entries linked to this study.
Ligier F, Guillemin F, Angot C, Bourion S, Kabuth B. Recurrence of suicide attempt in adolescents lost to contact early by clinicians: The 10-year REPEATERS cohort of French adolescents. J Adolesc. 2015 Aug;43:111-8. doi: 10.1016/j.adolescence.2015.05.011. Epub 2015 Jun 12.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
u000420
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.