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Emotion Regulation Individual Therapy for Adolescents With NSSI - An Open Pilot Study

Emotion Regulation Individual Therapy for Adolescents With NSSI - An Open Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02326012
Enrollment
17
Registered
2014-12-25
Start date
2014-03-31
Completion date
2016-01-31
Last updated
2016-01-05

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

Conditions

Nonsuicidal Self-Injury

Brief summary

The primary aim is to investigate the effectiveness of Emotion Regulation Individual Therapy for Adolescents (ERITA) who self-harm.

Interventions

BEHAVIORALEmotion Regulation Individual Therapy for Adolescents

Sponsors

Karolinska Institutet
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
13 Years to 17 Years
Healthy volunteers
No

Inclusion criteria

* a primary diagnosis of NSSI as defined by DSM-5 Section 3 * \< 1 NSSI episode during the past month * at least one parent needs to commit to participate in the parent program

Exclusion criteria

* bipolar disorder I or primary psychosis * severe suicidal ideation * ongoing substance dependence * Insertion/withdrawal of psychopharmacological substances within two months prior to the treatment * other acute primary axis I diagnosis (e.g. anorexia nervosa) that demand treatment in first hand * current life circumstances that would hinder the treatment (i.e. ongoing domestic abuse) * insufficient Swedish language skills * Cocurrent treatment with Mentalization based therapy (MBT) or Dialectical behavioral therapy (DBT)

Design outcomes

Primary

MeasureTime frameDescription
Deliberate Self-Harm Inventory - 9 item versionBaseline (7 days prior to treatment start), weekly (once a week following treatment start), post-treatment (12 weeks) and six months follow-upChange from baseline in self-harming behaviors when measures weekly, after 12 weeks and at 6 months after treatment has ended.

Secondary

MeasureTime frameDescription
Difficulties in Emotion Regulation Scale -16 item version (DERS-16)Baseline (7 days prior to treatment start), weekly (once a week following treatment start), post-treatment (12 weeks) and six months follow-upChange from baseline in difficulties in emotion regulation when measures weekly, after 12 weeks and at 6 months after treatment has ended.
Diary questionnaire (DQ)Baseline (7 days prior to treatment start), weekly (once a week following treatment start), post-treatment (12 weeks) and six months follow-upChange from baseline in difficulties in emotion regulation when measures weekly, after 12 weeks and at 6 months after treatment has ended.
Difficulties in Emotion Regulation Scale (DERS)Baseline (7 days prior to treatment start), post-treatment (12 weeks) and six months follow-upChange from baseline in difficulties in emotion regulation after 12 weeks and at 6 months after treatment has ended.
Strengths and Difficulties Questionnaire Child and Parent version (SDQ-C/P)Baseline (7 days prior to treatment start), post-treatment (12 weeks) and six months follow-upChange from baseline in strengths and difficulties after 12 weeks and at 6 months after treatment has ended.
Borderline personality features in childhood (BPFS-C)Baseline (7 days prior to treatment start), post-treatment (12 weeks) and six months follow-upChange from baseline in borderline personality features after 12 weeks and at 6 months after treatment has ended.
The alcohol use disorders identification test - C (AUDIT-C)Baseline (7 days prior to treatment start), post-treatment (12 weeks) and six months follow-upChange from baseline in alcohol use after 12 weeks and at 6 months after treatment has ended.
Evaluation of the Drug Use Disorders Identification Test - C (DUDIT-C)Baseline (7 days prior to treatment start), post-treatment (12 weeks) and six months follow-upChange from baseline in drug use after 12 weeks and at 6 months after treatment has ended.
Borderline Symptom List Behavior supplement (BSL-supplement)Baseline (7 days prior to treatment start), weekly (once a week following treatment start), post-treatment (12 weeks) and six months follow-upChange from baseline in self-destructive and risky behaviors when measures weekly, after 12 weeks and at 6 months after treatment has ended.

Other

MeasureTime frameDescription
Patient Health Questionnaire (PHQ9)Baseline (7 days prior to treatment start), post-treatment (12 weeks) and six months follow-upChange in patient parent health from baseline after 12 weeks and at 6 months after treatment has ended.
General Anxiety Disorder (GAD7)Baseline (7 days prior to treatment start), post-treatment (12 weeks) and six months follow-upChange in patient parent health from baseline after 12 weeks and at 6 months after treatment has ended.
The treatment credibility scaleOne week after treatment startPerceived treatment credibility
Working Alliance Inventory (WAI) short versionThree weeks after treatment startPerceived working alliance
Trimbos/iMTA questionnaire for Costs associated with Psychiatric Illness - Child version (TiC-P)Baseline (7 days prior to treatment start), post-treatment (12 weeks) and six months follow-upChange from Baseline in societal costs after 14 weeks and at 6- and 12 months after treatment has Change from baseline in quality of life after 12 weeks and at 6 months after treatment has ended. Used for health economic evaluations.
Euroqol-5D (EQ-5D)Baseline (7 days prior to treatment start), post-treatment (12 weeks) and six months follow-upChange from Baseline in quality of life after 14 weeks and at 6- and 12 months after treatment has Change from baseline in quality of life after 12 weeks and at 6 months after treatment has ended. Used for health economic evaluations.

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 25, 2026