MedTrace Logo

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

NCT07568717 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2026-05-06

No results posted yet for this study

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.

Conditions

  • Sexual Abuse
  • Posttraumatic Stress Symptom
  • Sexual Trauma
  • Partner

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 & Collaborators

  • University of Agder

    collaborator OTHER

  • NTNU Health (sponsor)

    collaborator UNKNOWN

  • Sykehuset Telemark

    lead OTHER_GOV

Principal Investigators

  • Hege Kersten, PhD · Sykehuset Telemark

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-08-27
Primary Completion
2026-09-30
Completion
2028-12-31

Countries

  • Norway

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07568717 on ClinicalTrials.gov