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Group therapy for adolescents who repeatedly harm themselves

A two arm single blinded randomised allocation trial of a manualised group therapy in addition to usual care compared with usual care alone for adolescents who repeatedly harm themselves

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN20496110
Enrollment
372
Registered
2009-08-19
Start date
2002-08-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Self-harm (deliberate overdoses, cutting, burning, banging head, ligatures) Mental and Behavioural Disorders Self-harm

Interventions

Intervention: The experimental group therapy intervention is a manualised treatment specifically designed for adolescents who harmed themselves. The group treatment is based on cognitive behaviour and

Sponsors

University of Manchester (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 12 - 17 years, either sex 2. Referred to mental health services in Greater Manchester following self-harm 3. The adolescent reports that in the last year he or she has harmed themselves on at least one other occasion

Exclusion criteria

Exclusion criteria: 1. The adolescent cannot attend groups (e.g., in secure care) 2. Has a psychotic or eating disorder 3. Unlikely to benefit from groups (e.g., learning problems) 4. Non-English speakers

Design outcomes

Primary

MeasureTime frame
Frequency and severity of episodes of self harm assessed using an adapted self harm interview schedule. Steps will be taken with the interview schedule to minimise a recall bias towards more recent events and to get a clear picture of the pattern of self harm over the previous year. The self harm interview will be conducted by research assessors (blinded to treatment allocation) and additionally (to allow for reporting bias from young people) clinicians involved with the young person will also undertake the same interview.

Secondary

MeasureTime frame
1. Time to first and second repetition, number of severe suicidal acts (defined by medical risk of death) 2. Depression measured using the Moods and Feelings Questionnaire (MFQ) 3. Suicidality measured using the Suicidale Ideation Questionnaire 4. Global outcome assessed by the health of the nation outcome scales for children and adolescents (HoNOSCA) 5. Psychosocial stress assessed using the Kiddie Schedule for Affective Disorders and Scizophrenia (K-SADS) 6. Cost benefit analysis measured using the Service Use Inventory All the above administered at baseline, 6 and 12 months. At 3 months an assessment to measure emerging personality problems was undertaken (SCID II).

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026