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Healing Together: Partners' Experiences in the Journey of Sexual Trauma Recovery Through the Intervention Take Your Sexuality Back for Sexually Traumatized Women.

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

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07568717
Enrollment
12
Registered
2026-05-06
Start date
2025-08-27
Completion date
2028-12-01
Last updated
2026-05-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Partner, Posttraumatic Stress Symptom, Sexual Abuse, Sexual Trauma

Brief summary

This study aims to gain insight into the experiences of partners to participants in the "Take Your Sexuality Back" intervention groups, evaluate the intervention's acceptability, and identify necessary modifications. This study is part of a larger project that seeks to establish a scientific basis for this innovative, group-based treatment to help women who have experienced sexual trauma heal their sexuality. Before implementing the intervention in the healthcare system and initiating a larger randomized controlled trial, the investigators will evaluate the intervention's feasibility and potential efficacy, as well as gain a more comprehensive understanding of treatment outcomes. In addition to collecting quantitative data, it is crucial to gather qualitative data on participants' and participants partners´ experiences. In this study, data will be obtained through in-depth interviews with partners´ to group participants after they complete the intervention.

Interventions

BEHAVIORAL"Take your sexuality back"

The intervention is trauma-sensitive and focus both on traumatized sexuality and positive sexuality. It incorporates regulatory skills to prevent re-traumatization when addressing sex-positive themes, thus accommodating a wide range of trauma-related symptoms, sexual shame, sexual dysfunctions, and regulation difficulties. The intervention integrates psychoeducation, exercises, reflections and sharing. The intervention include partners to participants in two of the sessions.

Sponsors

Sykehuset Telemark
Lead SponsorOTHER_GOV
University of Agder
CollaboratorOTHER
NTNU Health (sponsor)
CollaboratorUNKNOWN

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Being partner of a participant in the intervention group.

Exclusion criteria

* Living in an abusive relationship with the participant in the intervention group

Design outcomes

Primary

MeasureTime frameDescription
What are the partners' experiences of participating in the intervention and of being witness to and taking part in their partners (participants) process during the intervention?1-2 weeks after participants have completed the intervention.In-depth interviews investigating partners´ experiences and perspectives of the intervention groups, with the aim of identifying areas for potential improvement in the intervention and specifically how partners can best be involved in the rehabilitation process. Interviews will be analyzed through a descriptive phenomenological method.

Countries

Norway

Contacts

STUDY_DIRECTORHege Kersten, PhD

Sykehuset Telemark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 7, 2026