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Study identifier: NCT06099561 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Intractable Self-harm-What Support is Effective?

Condition: Self-harm  ·  Sponsor: Region Skane

PhaseN/A
Planned participants30
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The aim of this project is to evaluate a novel treatment program for individuals with intractable and lethal self-harm. The main questions are: 1: Is there, in individuals with intractable self-harm, a relevant improvement in daily functioning and is this improvement related to the provided interventions? The secondary research questions are: 2\. Is there, in individuals with intractable self-harm, a relevant improvement in frequency and severity of self-harm? 3\. Is there, in individuals with intractable self-harm, a relevant improvement in voluntary hospital admissions? 4\. Is there, in individuals with intractable self-harm, a relevant improvement in compulsary hospital admissions? 5\. Is there, in individuals with intractable self-harm, a relevant improvement in the use of medication pro re nata? 6\. Is there, in individuals with intractable self-harm, a relevant improvement in cost-effectiveness related to the provided interventions?

This description comes directly from the study's public registry record.

Talk to the study team

Magnus Nilsson, PhD  ·  046-174925  ·  magnus.per.nilsson@skane.se

Sofie Westling, MD/PhD  ·  sofie.westling@skane.se

Always discuss trial participation with your own doctor first.

Locations (1)

National Highly Specialized Unit for Self-Harm Behaviours, SkåneLund, Skåne County, SwedenRecruiting

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Source record: clinicaltrials.gov/study/NCT06099561