Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06133569

ReDirection - Self Help Program for Individuals with Sexual Interest in Children

Led by Karolinska Institutet · Updated on 2024-10-10

60

Participants Needed

6

Research Sites

54 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 aim of the study is to evaluate the effectiveness of the ReDirection program for individuals with low or medium risk to commit child sexual abuse. Primary question: Is ReDirection a feasible, effective, and safe method in reducing low to medium risk participants' use of CSAM and related behaviors?

CONDITIONS

Official Title

ReDirection - Self Help Program for Individuals with Sexual Interest in Children

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Sufficient language skills: English, Swedish, Finnish, Czech, Slovak, German, or Spanish
  • concern about sexual interest regarding children*,
  • CSAM use past six month
  • Low to medium risk for committing child sexual abuse according to the SChiMRA scale
Not Eligible

You will not qualify if you...

- Participants with a severe psychiatric illness (such as high acute suicide risk or severe substance abuse) will be excluded, or lack of serious intentions to participate.

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Trial Site Locations

Total: 6 locations

1

National Institute of Mental Health

Klecany, Czechia

Actively Recruiting

2

Protect Children NGO

Helsinki, Finland

Actively Recruiting

3

[University Medical Center Hamburg-Eppendorf

Hamburg, Germany

Actively Recruiting

4

Bratislava Police Academy

Bratislava, Slovakia

Actively Recruiting

5

Universitat Jaume I

Castelló, Spain

Actively Recruiting

6

Centre for psychiatry research, Region Stockholm

Stockholm, Sweden, 11842

Actively Recruiting

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Research Team

C

Christoffer Rahm, MD, PhD

CONTACT

M

Maria Breide

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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