National Highly Specialized Care for Severe Self-Harm and Eating Disorders in Swedish Youth

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This prospective, observational study evaluates National Highly Specialized Care (NHV) provided at two Stockholm services for youths with severe self-harm or eating disorders. It uses qualitative interviews at treatment completion and one year later to capture patient and parent experiences, alongside secondary measures of feasibility, adherence, and changes in symptoms and functioning. NHV typically involves 12–13 weeks of intensive inpatient and psychotherapeutic treatment tailored by multidisciplinary teams, with approaches like DBT, FBT, or CBT as clinically appropriate. Data are collected during routine clinical care rather than mandated by the research protocol, focusing on real-world outcomes and experiences. The study aims to identify barriers to successful treatment and how NHV can facilitate transition to less intensive care when possible.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* Children and adolescents aged 13-17 years who meet the eligibility criteria for and are receiving National Highly Specialized Care (NHV) for severe self-harm or eating disorders at one of the participating clinical units.
* Parents or legal guardians of children and adolescents receiving NHV at the participating clinical units.
* Informed consent to study participation, according to applicable procedures.

Exclusion Criteria:

* Acute medical or psychiatric conditions requiring immediate healthcare interventions that temporarily preclude study participation.
* Inability to independently complete study questionnaires, for example due to language-related difficulties.

Where it's running

• Stockholm's child and adolescent psychiatry (BUP Stockholm)
  Stockholm, Sweden Recruiting
• Stockholm Centre for Eating Disorders (SCÄ)
  Stockholm, Sweden Recruiting

Study contacts

• Principal investigator: Martina Wolf-Arehult, PhD — Karolinska Institutet
• Study coordinator: Sanna Marek, MSc
• Email: sanna.marek@regionstockholm.se
• Phone: +46812353170

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

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• FlexED: Full Threshold Body-Image Intervention for Young Women

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  Recruiting Duke University · Durham, North Carolina · NCT07732829

• Four CBT-E formats for Binge Eating Disorder in adults

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.