Condition: Self-harm · Personality Disorder, Borderline · Epigenetic Disorder · Sponsor: University of Ljubljana, Faculty of Medicine
In the proposed study, three objectives will be pursued: 1. To develop a method to identify more effectively the acute and long-term risk of adolescents with the most threatening self-harm behaviours. 2. To identify the factors that influence the risk of self-harm behaviours and the success of treatment/treatment of these behaviours in the most at-risk adolescents (changes in these factors). 3. Develop guidelines for more effective treatment of the most at-risk adolescents. For this purpose, a sample of approximately 200 young people who will be hospitalised for suicide risk (the most at risk in Slovenia) and an approximately equal number of healthy adolescents will be included. At inclusion, the presence of several factors will be assessed by reviewing demographic data, clinical diagnosis, self-assessment questionnaires and clinical psychological tests (CSSRS, B-NSSI-AT, ISAS, LPFS-BF2.0, BPFSC-11, TSCC, PAI, ECR-RS, DASA-YV, ASHRS), social assessment, and blood sampling for genetic analyses (DNA isolation, sequencing, nucleotide sequence recognition, quantification and evaluation of short tandem repeats, identification of methylation sites). Longitudinal tracking of autoaggressive events and heteroaggressive events during hospitalisation will be performed and recorded on an ongoing basis. The risk and protective factors of the adolescents most at risk will be compared with a control group of adolescents. The same factors will be reassessed in the most at-risk adolescents …
This description comes directly from the study's public registry record.
Maja Drobnič Radobuljac · 015874840 · maja.radobuljac@psih-klinika.si
Maja Drobnič Radobuljac · maja.radobuljac@psih-klinika.si
Always discuss trial participation with your own doctor first.
| Medical Faculty - University of Ljubljana | Ljubljana, Slovenia | Active Not Recruiting |
| University Psychiatric Clinic Ljubljana | Ljubljana, Slovenia | Recruiting |
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Source record: clinicaltrials.gov/study/NCT05765864