ClinicalTrials.gg
RecruitingNCT06315075Updated Aug 31, 2026

Dialectical Behavior Therapy for Adolescents With Self-harm and Suicidal Behavior- an Open Trial

An interventional study of Dialectical behavior therapy for adolescents (DBT-A) in Self-harm, Suicidal Ideation and Suicide and Self-harm, sponsored by Haukeland University Hospital. Recruiting at 1 site in Norway. Open to participants aged 13 Years to 18 Years. Per ClinicalTrials.gov, last updated 2026-08-31.

Primary conditionSuicidal IdeationRegistry: Self-Injurious BehaviorReclassifiedWhy we changed it
Registry
Self-Injurious Behavior — the first condition term the registry derived for this study.
ClinicalTrials.gg
Suicidal Ideation
Why
  1. The study's listed conditions name Suicidal Ideation, a narrower term within Self-Injurious Behavior.
Confidence
High: the new condition is named in the study's own listed conditions. Of 351 hand-checked studies reclassified this way, 68% were exactly right and 84% in the right disease family; the registry's first term was right for 5% (measured 2026-10-21). How we classify →
Wrong?
Tell us the study's main condition →

Sponsored by Haukeland University Hospital · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Jan 2024; still recruiting 2 years 9 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
140
Allocation
Not applicable
Ages
13 Years to 18 Years
Sex
All
01

Study summary

The goal of this pre-post-follow-up study is to examine how well the treatment Dialectical behavior therapy for adolescents (DBT-A) with a duration of 20 weeks for adolescents with self-harm and suicidal behavior works in routine clinical practice. The main questions it aims to answer are:

  • to investigate how well DBT-A works after treatment and at 3-month follow-up, measured by episodes of self-harm, suicide attempts, depressive symptoms and quality of life, drop-out from treatment and number of possible participants who decline DBT-A.
  • to investigate how well DBT-A works at 12 months follow-up
  • to investigate whether pre-treatment factors can predict who will benefit from treatment
Read the detailed description

Self-harm and suicidal ideation are prevalent among adolescents and associated with major mental health problems and adverse life events. Dialectical behavior therapy for adolescents (DBT-A) is an empirically supported treatment for self-harm and suicidal ideation in adolescents. However, knowledge is scarce on the effectiveness, long-term outcomes, acceptability, and dropout of DBT-A when implemented and delivered as part of routine clinical practice in the Norwegian national health care system. The main aim of this study is to examine the outcomes from DBT-A in terms of self-harm episodes, suicide attempts, and emergency hospital admission, in addition to acceptability and dropout, when DBT-A is delivered at the Department of Child and adolescent psychiatry (PBU), Haukeland University Hospital (HUS). The study is an uncontrolled pre-post study with one-year follow-up and includes three aims: to evaluate outcomes of DBT-A up to three months post-treatment, at one-year follow-up, and to describe predictors of outcome for adolescents receiving DBT-A.

02

Conditions studied

  • Self-harm
  • Suicidal Ideation
  • Suicide and Self-harm

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Keywords

  • Suicide and Self-harm
  • Adolescents
  • Dialectical behavior therapy for adolescents
  • Routine clinical practice
  • Effectiveness study
03

In context

Suicidal Ideation Reclassified

569 studies on the registry are indexed under Suicidal Ideation; 203 are open to participants now.

This study's planned enrollment of 140 is above the median of 80 across 469 interventional studies indexed under Suicidal Ideation.

Browse Suicidal Ideation studies →

Lead sponsor

Haukeland University Hospital is the lead sponsor of 284 studies on the registry; 59 are open to participants now.

Compared within Suicidal Ideation, this study's primary condition as ClinicalTrials.gg classifies it; the registry's first condition term is Self-Injurious Behavior. The counts are of registry records indexed under each term, refreshed daily. How we classify →

04

Who can participate

Ages eligible
13 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age 13-18 years
  • Ongoing or a history of self-harm the last six months; current suicidal behavior (suicidal thoughts or at least one suicide attempt within the previous six months); at least three criteria of Diagnostic and Statistical Manual -5 () Borderline personality disorder (BPD), or the self-destruction criterion of DSM-5 BPD in addition to minimum two subthreshold criteria as assessed by the Structured Clinical Interview for DSM-5 Personality Disorders (SCID-5-PD) (First et al., 2016)
  • Fluency in Norwegian
  • One parent/trusted adult that can participate together with the adolescent.

Exclusion criteria

Exclusion Criteria:

  • Intellectual disability
  • Significant learning or language impairments
  • Autism spectrum disorder
  • Anorexia Nervosa
  • Any psychotic disorder
  • Substance abuse disorder. These patients will be offered treatment as usual at their local outpatient clinic.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

DSM diagnostic criteria

The American Psychiatric Association’s manual of mental health diagnoses. DSM-5 (2013, revised as DSM-5-TR in 2022) replaced DSM-IV, and some studies still name the older edition. “Meets DSM criteria for …” means diagnosed by that edition’s diagnostic criteria, usually by a clinician in an interview.

05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
140 participants (estimated)

Study arms

  • Experimental
    DBT-A

    Single group uncontrolled study. All participants will receive DBT-A

    Behavioral: Dialectical behavior therapy for adolescents (DBT-A)

Interventions

  • BehavioralDialectical behavior therapy for adolescents (DBT-A)

    A 20-week DBT-A with a weekly individual session (45 minutes), a weekly session of multifamily skills training groups with a caregiver (120 minutes), and telephone consultation with individual therapists outside therapy sessions as needed. The treatment consists of four components and is delivered according to the manual except for the phone coaching that PBU offers workdays until 8 pm.

    Also known as: DBT-A

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What researchers measure

Primary outcomes

  1. Functional Assessment of Self-Mutilation (FASM)

    Number of self-harm episodes in the last four weeks categorized by intention and self-harm method, number of suicide attempts, and number of emergency department visits caused by suicidal behavior. In addition, FASM includes functional assessment of self-mutilation.

    Time frame: pre, after 20 weeks DBT-A ("post"), at 3 and 12 months follow-up

  2. Number of participants in need of emergency department visits caused by suicidal behavior

    Medical record data extraction

    Time frame: pre, after 20 weeks DBT-A ("post"), at 3 and 12 months follow-up

Secondary outcomes

  1. Depressive symptom score measured by Short Mood and Feelings questionnaire (SMFQ)

    Depressive symptoms. SMFQ includes 13 items, measured on a 0-2 Likert scale, with higher scores indicating a higher level of depressive symptoms.

    Time frame: pre, after 20 weeks DBT-A ("post"), 3 and 12 months follow-up

  2. Health related quality of life measured by SCREENing for and Promotion of Health Related Quality of Life in Children an Adolescents (Kidscreen 10)

    Kidscreen includes 10 items measured on a 5 point Likert scale and gives a global measure from 0-100 of health-related quality of life in addition to the individual aspects. Higher scores reflects higher health related quality of life.

    Time frame: pre, after 20 weeks DBT-A ("post"), 3 and 12 months follow-up

  3. Barriers to Treatment Participation Scale (BTPS) score

    The BTPS questionnaire evaluate reasons for treatment discontinuation, and treatment participation barriers.

    Time frame: pre, at dropout at any time between session 1 and end of treatment at session 20.

  4. Perceived benefit of skills training in DBT-A measured by a study specific questionnaire.

    Perceived benefit of skills training in DBT-A is a study-specific patient- and parent reported evaluation measure of perceived benefits of DBT-A components rated on a 0-5 Likert scale.

    Time frame: At dropout at any time between session 1 and end of treatment at session 20, or for completers after 20 weeks DBT-A ("post"),

07

Study locations

1 of 1 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 31, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06315075
Responsible party
Sponsor
First posted
Mar 18, 2024
Start date
Jan 15, 2024
Primary completion
Dec 31, 2027 (estimated)
Completion
Dec 31, 2029 (estimated)
Last update
Aug 31, 2026

Study contacts

Gro Janne H. Wergeland, MD, PhD
Contact
gneh@helse-bergen.no
+47 48176828
Anne Mari Syversen, Psychol
Contact
anne.mari.syversen@helse-bergen.no
+47 55975000
Gro Janne H. Wergeland, MD, PhD
principal investigator · Haukeland University Hospital

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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