This study looks at the potential effects of a new group treatment called "Take Your Sexuality Back", designed for women who have experienced sexual trauma. Investigators will collect information in two ways-through forms that participants fill out themselves and through ECG measurements during a stress tests. Data will be collected before the treatment, right after it, and again three months later. When all data are collected and analyzed investigators will carry out in-depth interviews with participants and explore how they felt about being tested and how they understand the results -especially if some numbers look unusual or surprising. The goal with this study is to create a strong foundation for a future larger-scale study of the treatment by testing the methods, estimating the size of possible effects and identify outcome measurements that are experienced as meaningful to the participants.
Age range
18 Years
Sex
FEMALE
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
PTSD-symptoms and complex PTSD symptoms
Timeframe: From enrollment to 3 month after end of treatment (12 weeks treatment)
Sexual satisfaction
Timeframe: From enrollment to 3 months after end of treatment (12 weeks intervention)
Sexual shame
Timeframe: From enrollment to 3 months after end of treatment (12 weeks intervention).
Interoceptive awareness
Timeframe: From enrollment to 3 months after end of treatment (12 weeks intervention).
Responses to script-driven imagery.
Timeframe: From enrollment to 3 months after end of treatment (12 weeks intervention).
Touch body map
Timeframe: From enrollment to 3 months after end of the treatment (12 weeks intervention).
Change in HRV and SampEn from pre-post and at follow up efter 3 month.
Timeframe: Enrollment to 3 months after end of treatment (12 weeks intervention).
Participants experiences of being tested and their understanding of the results.
Timeframe: Three month after end of treatment, when all quantitative results are analyzed and calculated.