跳至主要内容
临床试验/NCT06607042
NCT06607042尚未招募不适用

BEDIT-RCT: Randomized Controlled Study on the Effectiveness of Berlin Dissexuality Therapy as Part of the Model Project in Accordance With §65d German Social Security Code V

Charite University, Berlin, Germany0 个研究点目标入组 60 人开始时间: 2024年9月16日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
60
主要终点
Abstinence

研究概览

简要总结

The main goal of this clinical trial is to learn if psychotherapy works to reduce consumption of child abuse imagages.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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

排除标准

  • 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.

结局指标

主要结局

Abstinence

时间窗: From enrollment to the end of treatment 12 - 18 weeks

Abstinence rates for the consumption of abusive images

次要结局

  • Frequency of abstinence rates(From enrollment to the end of treatment 12 - 18 weeks)
  • Sexual preoccupation(From enrollment to the end of treatment 12 - 18 weeks)
  • Cognitive distortions about child sexual abuse(From enrollment to the end of treatment 12 - 18 weeks)
  • Emotion regulation(From enrollment to the end of treatment 12 - 18 weeks)
  • Mental Health(From enrollment to the end of treatment 12 - 18 weeks)
  • General well-being(From enrollment to the end of treatment 12 - 18 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Klaus Michael Beier

Director, Institute for Sexual Research and Sexual Medicine

Charite University, Berlin, Germany

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