Actively Recruiting

Phase Not Applicable
Age: 15Years - 18Years
All Genders
NCT06306586

A Digital Treatment for Adolescents With Eating Disorders

Led by Haukeland University Hospital · Updated on 2025-12-22

60

Participants Needed

3

Research Sites

146 weeks

Total Duration

On this page

Sponsors

H

Haukeland University Hospital

Lead Sponsor

H

Helse Fonna

Collaborating Sponsor

AI-Summary

What this Trial Is About

The goal of this feasibility study is to evaluate the feasibility and preliminary clinical outcomes of a personalized digital treatment for adolescents with eating disorders. The main objectives are to: i) Evaluate whether a personalized digital treatment for adolescents with eating disorders are feasible in a child and adolescent psychiatric outpatient clinic. ii) Evaluate who benefits from a personalized digital treatment for adolescents with eating disorders (what works for whom?) iii) Evaluate the cost-benefit of a personalized digital treatment for adolescents with eating disorders. Participants will be enrolled in a 10-week digital treatment including weekly therapist contact. They will be asked to complete self-report questionnaires at pre-, during, post- and 3- and 6-months follow-up.

CONDITIONS

Official Title

A Digital Treatment for Adolescents With Eating Disorders

Who Can Participate

Age: 15Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Diagnosed with atypical anorexia nervosa, atypical bulimia nervosa, other eating disorders, or unspecified eating disorder
  • Aged between 15 and 18 years
  • Stable dose of medication for co-morbid psychiatric treatment for at least six weeks and still meet study entry criteria
  • Have internet access
  • Speak and write Norwegian
Not Eligible

You will not qualify if you...

  • Diagnosed with anorexia nervosa or bulimia nervosa
  • Disorders of psychological development (F80-F89)
  • Avoidant restrictive food intake disorders
  • Co-morbid medical conditions or disorders affecting eating or weight (e.g., pregnancy, cancer), psychotic disorders, acute suicidality, substance abuse or dependence, or severe depressive episode
  • Receiving inpatient or face-to-face psychological treatment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 3 locations

1

Bømlo Kommune

Bømlo, Vestland, Norway

Withdrawn

2

Haukeland University Hospital

Bergen, Norway

Actively Recruiting

3

Helse Fonna

Haugesund, Norway

Completed

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Research Team

E

Emilie Nordby, MA

CONTACT

G

Guri Holgersen, MA

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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