Actively Recruiting
Intractable Self-harm-What Support is Effective?
Led by Region Skane · Updated on 2026-04-29
30
Participants Needed
1
Research Sites
173 weeks
Total Duration
On this page
Sponsors
R
Region Skane
Lead Sponsor
D
Department of Psychology. Lund University.
Collaborating Sponsor
AI-Summary
What this Trial Is About
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?
CONDITIONS
Official Title
Intractable Self-harm-What Support is Effective?
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Having tried or made serious attempt to try at least two different interventions with evidence to reduce self-harm, without sufficient reduction in suffering or self-harm
You will not qualify if you...
- Need for translation services to complete measures or interviews
- Not able to complete measures or interviews
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
National Highly Specialized Unit for Self-Harm Behaviours, Skåne
Lund, Skåne County, Sweden, 22185
Actively Recruiting
Research Team
M
Magnus Nilsson, PhD
CONTACT
S
Sofie Westling, MD/PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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