Status:
NOT_YET_RECRUITING
Study on the Effectiveness of Berlin Dissexuality Therapy as Part of the Model Project in Accordance With §65d SBG V
Lead Sponsor:
Charite University, Berlin, Germany
Collaborating Sponsors:
Hannover Medical School
Heinrich-Heine University, Duesseldorf
Conditions:
Paedophilia
Hebephilia
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
The main goal of this clinical trial is to learn if psychotherapy works to reduce consumption of child abuse imagages.
Eligibility Criteria
Inclusion
- Age at first presentation minimum 18 years
- Voluntary consent to participation on the part of the participant
- At the time of inclusion, no contact with the justice system (ongoing investigation, ongoing criminal proceedings, ongoing prison sentence) due to sexually abusive behavior towards children
- Sexually conspicuous behavior and/or fantasies or impulses that indicate the presence of a pedophilic and/or hebephilic preference disorder.
- An offer of treatment is made when a suspected diagnosis is confirmed or the diagnosis is confirmed
- Feared or recent use of abusive images
- Sufficient knowledge of German
- Voluntary participation in the study and checking the checkbox in the informed consent form before starting participation
Exclusion
- Age under 18 years
- Lack of consent on the part of the patient
- Exclusion of the presence of a pedophilic and/or hebephilic preference disorder
- Current legal status in the sense of an ongoing investigation or criminal proceedings due to sexually assaultive behavior towards children
- Severe comorbidities: unstable psychotic disorder, organic brain damage, reduced intellectual capacity (IQ below 70), untreated drug or alcohol addiction or persistent harmful use
- Current risk of child sexual abuse and or child sexual abuse that occurred less than 15 years before the start of the study
- An antiandrogenic medication or an opiate antagonist, during therapy start taking a serotonin reuptake inhibitor.
Key Trial Info
Start Date :
September 16 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 31 2025
Estimated Enrollment :
60 Patients enrolled
Trial Details
Trial ID
NCT06607042
Start Date
September 16 2024
End Date
December 31 2025
Last Update
September 23 2024
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