Actively Recruiting

Phase Not Applicable
Age: 13Years - 17Years
All Genders
NCT06817278

Internet-delivered Emotion Regulation Individual Therapy or Adolescents (IERITA) With Self-injury Within Child and Adolescent Mental Health Services: Pilot Study

Led by Karolinska Institutet · Updated on 2026-05-04

100

Participants Needed

1

Research Sites

97 weeks

Total Duration

On this page

Sponsors

K

Karolinska Institutet

Lead Sponsor

R

Region Stockholm

Collaborating Sponsor

AI-Summary

What this Trial Is About

The overall purpose of the study is to implement and evaluate IERITA (Internet-delivered Emotion Regulation Individual Therapy for Adolescents) within child and adolescent mental health services for adolescents engaging in nonsuicidal self-injury (NSSI) and to optimize treatment outcomes for those adolescents at risk of insufficient effects. The specific purpose of this pilot trial is to investigate feasibility in preparation for a larger trial.

CONDITIONS

Official Title

Internet-delivered Emotion Regulation Individual Therapy or Adolescents (IERITA) With Self-injury Within Child and Adolescent Mental Health Services: Pilot Study

Who Can Participate

Age: 13Years - 17Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age between 13 and 17 years old
  • At least one episode of self-injury in the past three months
  • A parent willing to participate in the parent program
Not Eligible

You will not qualify if you...

  • Immediate risk of suicide
  • Global functioning score of 40 or below on the Children's Global Assessment Scale (CGAS)
  • Social problems requiring immediate intervention, such as family violence
  • Currently receiving dialectical behavior therapy for adolescents

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Karolinska Institutet

Stockholm, Sweden, 113 64

Actively Recruiting

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Research Team

O

Olivia Ojala, PhD

CONTACT

J

Johan Bjureberg, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

DOUBLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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