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NCT Number: NCT06718387

Evaluation of the Impact of Participation in a Psycho-education Program for Victims of Sexual Violence

Evaluation of the impact of a psycho-education program for victims of sexual violence, to determine the most efficient model to patients.

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Key information

Conditions

PTSD Mental Disorders Sexual Violence Stress Disorders, Post-Traumatic Stress Disorders, Traumatic Therapeutic Alliance Trauma and Stressor Related Disorders

Age range

18 year–75 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

About this study

In 2022, CRP Sud NA set up a psycho-education group for victims of sexual violence (PE-VVS). Two groups were held, involving 10 patients:

  • Average age = 35 (29-50)
  • Average PCL5 before PE-VSS = 53 (31 - 63)
  • Type of SV experienced
  • In childhood or adolescence outside family environment
  • Incest
  • Rape in adulthood outside intimate relationship
  • Rape by intimate partner A special feature of this therapeutic group is the involvment of the CRP's patient-partner. He took part in both design and facilitation of the sessions, along with the two CRP co-therapists (IDE / psychologist).

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • At the suggestion of CRP therapists,
  • Patient treated at the CRP having been exposed to sexual violence

Exclusion criteria

-

Treatment and study plan

PsychoEducation Program

Other

6 sessions of PsychoEducational Program

Primary outcomes

  1. Evaluation of impact on quality of life (QoL) concerning participation in this psychoeducation program

    Time frame: 6 months after the end of program

    QoL measurement by Stages of Recovery Instrument "STORI"

  2. Evaluation of impact on self-esteem of participation in this psychoeducation program

    Time frame: 6 months after the end of program

    Self-esteem measurement by Rosenberg self-esteem scale

  3. Evaluation of Impact on mental well-being of participation in this psychoeducation program

    Time frame: 6 months after the end of program

    Well-being evalutation by Warwick-Edinburgh scale (WEMWBS)

Study contacts

Contact information is provided by the study sponsor or research team.

Celine PELEAU

CONTACT

[email protected]

05 56 56 35 78

Chantal BERGEY, MD

CONTACT

[email protected]

05 56 56 35 78

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Charles Perrens, Bordeaux

Other Gov

Registry information

Acronym: PE-VVS

Important dates

Study start
2023
Primary completion
2026
Study completion
2026
First posted
Dec 5, 2024
Registry last updated
Mar 16, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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