Clinical trial Recruiting at 1 site Interventional Ages 18 to 65 Women only

Voices of Transformation: Reclaiming sexuality after sexual trauma

Official title: Take Your Sexuality Back - a Feasibility Study of a New Intervention for Sexually Traumatized Women

Run by Sykehuset Telemark · NCT07165834 · Data updated 2026-11-12

This project will try a group program called "Take Your Sexuality Back" with adults who have experienced sexual trauma to see if it is acceptable and helpful for trauma-related sexual difficulties.

More Posttraumatic Stress Disorder trials

Quick facts

Study typeInterventional
Ages18 Years to 65 Years
SexWomen only
Enrollment20 (estimated)
SponsorSykehuset Telemark
Government
Locations1 site (Skien)
StatusRecruiting
StartedSeptember 15, 2025
Main results expectedSeptember 2026
Study endsDecember 2028
Registry record updatedMay 4, 2026
Trial IDNCT07165834 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are adults aged 18–65 with a history of sexual trauma who are experiencing trauma-related sexual problems, have sufficient Norwegian language skills to participate in a psychoeducational group, and do not meet exclusion criteria such as acute suicidality, severe substance abuse, severe dissociative or psychotic disorders, a current life crisis, or living in an abusive relationship.

Probably not a fit

People who are currently suicidal, have severe substance abuse that interferes with treatment, severe dissociative or psychotic disorders, an active life crisis, or who are living in an abusive relationship are unlikely to benefit from this group intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a feasibility and acceptability evaluation of the group-based "Take Your Sexuality Back" psychoeducational intervention for adults with a history of sexual trauma. Participants will take part in the group program and complete quantitative outcome measures to explore potential efficacy signals. After the intervention, researchers will conduct in-depth qualitative interviews to capture participants' experiences and identify needed modifications. The results will be used to refine the intervention and plan a larger randomized controlled trial and possible implementation in clinical services.

Why it matters

Potential benefit: If successful, the program could help people who have experienced sexual trauma regain sexual well-being, reduce trauma-related sexual problems, and improve quality of life.

How similar studies have gone: Group-based psychoeducational approaches for trauma-related sexual problems have some promising elements but are not yet well-established, so this approach is relatively novel and requires further testing.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. A history of sexual trauma
2. Experience trauma-related sexual problems
3. Age between 18 and 65 years
4. Enough competence in Norwegian to participate in a psychoeducational group.

Exclusion Criteria:

1. Acute suicidality
2. Serious substance abuse interfering with treatment
3. Severe dissociative or psychotic disorders
4. Current life crisis interfering with treatment
5. Living in an abusive relationship. -

Where it's running

  • Sykehuset Telemark HF
    Skien, Norway
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.