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A Group Based Psychoeducational Intervention for Partners of Child Sexual Abuse Material Offenders.

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Start date changed from estimate of Aug 31, 2026 to Aug 25, 2026v4
  2. Recruitment opened
    • Start date: Jun 15, 2026 to Aug 31, 2026
    • Site details revised
    v3
  3. Primary endpoint(s) modified
    • Start date: Mar 31, 2026 to Jun 15, 2026
    • Secondary endpoints: 5 to 9
    v2
  4. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The overall aim of this feasibility study is to investigate the clinical characteristics of female partners of male child sexual abuse material (CSAM) offenders and to evaluate the feasibility of a novel psychoeducational group intervention designed to address their specific needs. The main questions it aims to answer are: 1. What are the clinical characteristics of female partners of male CSAM offenders? 2. Is a psychoeducational group intervention for female partners of male CSAM offenders feasible? 3. Does a psychoeducational group intervention for female partners of male CSAM offenders provide any indication of effectiveness? Feasibility will be assessed in terms of 1) recruitment, time from recruitment to offered intervention and completed sessions 2) expectancy of treatment improvement, credibility, and satisfaction 3) acceptability and relevance 4) occurrence of negative effects 5) changes in depression- and anxiety symptoms and psychological well-being 6) changes in daily functioning.
Trial Details
NCT Number NCT07434219
Lead Sponsor Region Stockholm
Collaborators: Karolinska Institutet
Conditions
(from sponsor)		 Partner
Related terms Pedophilia
Enrollment 20 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov