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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02697019
Enrollment
25
Registered
2016-03-02
Start date
2016-02-29
Completion date
2017-12-31
Last updated
2018-08-10

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

Conditions

Nonsuicidal Self-Injury

Keywords

Nonsuicidal Self-Injury (NSSI), Deliberate Self-Harm (DSH), Self-harm, Self-injury

Brief summary

The primary aim is to investigate the effectiveness of an Internet-delivered Emotion Regulation Individual Therapy for Adolescents (ERITA) with nonsuicidal self-injury (NSSI).

Interventions

BEHAVIORALInternet-delivered Emotion 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 in Section 3 in the fifth edition of the Diagnostic and Statistical Manual 5 of the American Psychiatric Association (DSM-5) \< 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 (30 days prior to treatment start), weekly (once a week following treatment start), post-treatment (12 weeks), and three and six months follow-upChange from baseline in self-harming behaviors when measures weekly, after 12 weeks, and at 3 and 6 months after treatment has ended

Secondary

MeasureTime frameDescription
Borderline Symptom List Behavior supplement (BSL-supplement)Baseline (30 days prior to treatment start), weekly (once a week following treatment start), post-treatment (12 weeks), and three and six months follow-upChange from baseline in self-destructive behaviors when measures weekly, after 12 weeks, and at 3 and 6 months after treatment has ended
Difficulties in Emotion Regulation Scale -16 item version (DERS-16)Baseline (30 days prior to treatment start), weekly (once a week following treatment start), post-treatment (12 weeks), and three and six months follow-upChange from baseline in difficulties in emotion regulation when measures weekly, after 12 weeks, and at 3 and 6 months after treatment has ended
Difficulties in Emotion Regulation Scale (DERS)Baseline (7 days prior to treatment start), post-treatment (12 weeks), three and six months follow-up]Change from baseline in difficulties in emotion regulation after 12 weeks, at 3 and 6 months after treatment has ended
Borderline personality features in childhood (BPFS-C)Baseline (7 days prior to treatment start), post-treatment (12 weeks), three and six months follow-up]Change from baseline in symptoms of borderline personality disorder after 12 weeks, at 3 and 6 months after treatment has ended
The Revised Child Anxiety and Depression Scale - Child and Parent rated (RCADS-C)Baseline (7 days prior to treatment start), post-treatment (12 weeks), three and six months follow-up]Change from baseline in anxiety and depression after 12 weeks, at 3 and 6 months after treatment has ended
Suicidal Ideation Questionnaire (SIQ-JR)Baseline (7 days prior to treatment start), post-treatment (12 weeks), three and six months follow-up]Change from baseline in suicidal ideation after 12 weeks, at 3 and 6 months after treatment has ended
Acceptance and Action Questionnaire (AAQ-7)Baseline (7 days prior to treatment start), post-treatment (12 weeks), three and six months follow-up]Change from baseline in acceptance and action after 12 weeks, at 3 and 6 months after treatment has ended

Other

MeasureTime frameDescription
The treatment credibility scaleOne week after treatment startPerceived treatment credibility
Working Alliance Inventory (WAI) short versionThree weeks after treatment startPerceived working alliance
The Client Satisfaction Questionnaire (CSQ)Twelve weeks after treatment startPerceived client satisfaction
Adverse events12 weeks, and at 3 and 6 months after treatment has endedAdverse events
Adult ADHD Self-Report Scales (ASRS)At baselineSelf-reported symptoms of attention-deficit/hyperactivity disorder (ADHD)
Parental Psychological Flexibility (PPF) QuestionnaireBaseline (7 days prior to treatment start), post-treatment (12 weeks), three and six months follow-up]Change from baseline in parental psychological flexibility after 12 weeks, at 3 and 6 months after treatment has ended
The Coping with Children's Negative Emotions Scale Adolescent Version (CCNES-A)Baseline (7 days prior to treatment start), post-treatment (12 weeks), three and six months follow-up]Change from baseline in parental coping after 12 weeks, at 3 and 6 months after treatment has ended
The Parenting Sense of Competence (PSOC) ScaleBaseline (7 days prior to treatment start), post-treatment (12 weeks), three and six months follow-up]Change from baseline in parental coping after 12 weeks, at 3 and 6 months after treatment has ended

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026