Actively Recruiting
Sexual Agency of Women Who Have Suffered from Incest(s)
Led by Centre Hospitalier de Saint-Denis · Updated on 2024-10-15
10
Participants Needed
1
Research Sites
26 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Case study, qualitative and exploratory approach with prospective research. This study is aimed at voluntary patients referred by the women center. * The first meeting will be the presentation of a sexo-psychomotor questionnaire, specifically made for this study. Then, if the participant is willing, the enroll for a psychomotor follow-up of 6 sessions personalized with specific objectives defined for the patient,from the questionnaire. * These therapy sessions can be renewed in discussion with the woman if we feel they would benefit from further follow-up. The psychomotor sessions last around 45 minutes and take place once every 15 days or 3 weeks with a variety of therapeutical techniques. This interval between sessions allows time for integration of the aspects addressed during the proposals, while ensuring continuity in the follow-up. They are aimed at developing body and emotional awareness, to help patients get to know themselves better, and experience moments in full awareness * End-of-follow interview with taking the questionnaire a second time, to determine, with the woman, any benefits of the "sex-psychomotor" care. The women will be supported in completing the questionnaire again, as they were during the initial session.
CONDITIONS
Official Title
Sexual Agency of Women Who Have Suffered from Incest(s)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age > 18 years old
- Women who have suffered from incest or rape
- Speak and understand French
You will not qualify if you...
- Refusal to participate
- Non french-speakers
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Maison des femmes
Saint-Denis, Seine Saint Denis, France, 93200
Actively Recruiting
Research Team
E
Emma FONT
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here