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IRIS-A: A brief and easily applicable two-session smartphone app-supported program of Imagery Rescripting of Imagery Self-Injury – for Adolescents with nonsuicidal self-injury disorder (NSSID)

IRIS-A: A brief and easily applicable two-session smartphone app-supported program of Imagery Rescripting of Imagery Self-Injury – for Adolescents with nonsuicidal self-injury disorder (NSSID) - IRIS-A

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00025345
Enrollment
60
Registered
2021-06-24
Start date
2021-07-15
Completion date
Unknown
Last updated
2026-06-01

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

Conditions

nonsuicidal self-injury (NSSI)

Interventions

Group 1: "Imagery Rescripting"-intervention group (consisting of 2 sessions "Imagery Rescripting" for processing selfharming related imaginations). Pre-post survey as well as 3-month follow-up of ps

Sponsors

Klinikum Christophsbad
Lead Sponsor

Eligibility

Sex/Gender
All
Age
13 Years to 24 Years

Inclusion criteria

Inclusion criteria: - The presence of mental images of self-injury - NSSV research diagnosis according to DSM V - Participant age between 13 and 24 years (Kaess, Edinger, Fischer-Waldschmidt, Parzer, Brunner, & Resch, 2019) - Fluent in written and spoken German

Exclusion criteria

Exclusion criteria: - Reduced general health and below average IQ (IQ < 80). - Current psychotherapy or unwillingness to pause current psychotherapy for the duration of the examination (from T1 to T4). If current psychotherapy is paused, this will take place in consultation with the attending physician or psychotherapist. - Severe mental disorders such as schizophrenia-type disorders and bipolar affective disorders. - Acute suicidal tendencies - Dependency disorders (addiction disorder)

Design outcomes

Primary

MeasureTime frame
Reduction of self-injury Self-injurious thoughts and behaviours interview (SITBI) Measurement time points: Baseline, at the end of the second intervention session after 2 weeks, after one month and follow-up after 3 months.

Secondary

MeasureTime frame
Emotion regulation (FEEL-E, ERQ), emotional distress (Depressiveness - BDI II, anxiety – STAI-S), self-efficacy (WIRKALL_r), intrusive imagery (IFES-S), urge to self-harm (CEQ-SH), real-time imagery, app use frequency and duration. Assessment of safety: suicidality (C-SSRS) Control variables: social desirability (KSE-G) Acceptability of intervention (BIKEB; ZUF-8)

Countries

Germany

Contacts

Public ContactElisa Schmied

Universitätsklinikum Ulm, Klinik für Psychiatrie und Psychotherapie III

elisa.schmied@uniklinik-ulm.de015753667649

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Jun 11, 2026