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Triggers Online Resulting in Non-suicidal Self-Injury

Triggers Online Resulting in Non-suicidal Self-Injury - TORN

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00025905
Enrollment
75
Registered
2021-07-21
Start date
2022-05-01
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-Suicidal Self-Injury F60.3

Interventions

Group 1: Study 1: Ecological Momentary Assessment for one week with NSSI-patients. Study 2: Presenting neutral and NSSI-related stimuli for eyetracking in NSSI-patients. Study 3: Social exclusion (acc

Sponsors

Medizinische Universität Wien - Universitätsklinik für Kinder- & Jugendpsychiatrie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to 18 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria for the clinical group are (a) good German language skills, (b) fulfilling NSSI within the past 12 month after SITBI-G, (c) aged between 14;00 and 17;11 years. Inclusion criteria for the healthy controls are (a) good German language skills and (b) aged between 14;00 and 17;11 years.

Exclusion criteria

Exclusion criteria: Exclusion criteria for the clinical group are (a) adolescents treated with cortisone or suffering from a hormonal dysfunction, (b) fulfilling criteria for an Autism Spectrum Disorder (ASD), (c) IQ < 70 based on previous IQ-tests or clinical impression, (d) any known medical illness or other severe comorbid mental disorder requiring immediate treatment, (e) acute suicidality or severe aggression. Exclusion criteria for the healthy controls are (a) evidence of any current mental disorder or physical disease, (b) adolescents treated with cortisone or suffering from a hormonal dysfunction, (c) IQ < 70 based on previous IQ-tests or clinical impression, (d) acute suicidality or severe aggression.

Design outcomes

Primary

MeasureTime frame
Study 1: Urge/ideation to NSSI, NSSI frequency/intensity during 7 day period (EMA); Study 2: Urge/ideation to NSSI (self-rated), initial fixation & fixation time (both eye-tracking), autonomous response (SCR, HR) during experimental procedure; Study 3: Cortisol stress response, heart rate response, initial fixation & fixation time (eye-tracking) during experimental procedure.

Secondary

MeasureTime frame
Study 1: Mood, motives for NSSI (both, self-rated; ecological momentary assessment; duration: 7 days) Study 2: stress arousal/appraisal, positive and negative affect (all, self-rated), pupil dilatation (eyetracking) during experimental procedure Study 3: fundamental basic needs, stress arousal/appraisal, urge/ideation to NSSI (all, self-rated) during experimental procedure.

Countries

Austria

Contacts

Public ContactOswald Kothgassner

Medizinische Universität Wien - Universitätsklinik für Kinder- & Jugendpsychiatrie, SCAR-Unit

scar@meduniwien.ac.at+4314040032350

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: May 25, 2026