Self-Dehumanization and Hesitation to Report Domestic Violence
Condition(s) studied
Investigational drug(s) / intervention(s)
Questionnaires: Patients will undergo socio-demographic and history of violence suffered interview, passation of the Montgomery-Asberg Depression Rating Scale (MADRS),Childhood Trauma Questionnaire, Deshumanization Measure within Romantic Relationships scale, self-esteem scale, violentometer and an implicit association test (IAT).
Study summary
The patients included in the study will be adult women who are victims of domestic violence, consulting for this reason. The duration of participation of each patient will be one hour.
After obtaining the patient's non-opposition to her participation in the study, socio-demographic and history of violence suffered will be collected during an interview with the doctor/nurse. After that, the hetero-questionnaire MADRS (Montgomery-Asberg Depression Rating Scale) will be administered to the patient. This first part will last 30 minutes.
The second part of the study, carried out immediately after the interview, will be carried out on computer in the form of 4 self-questionnaires (Childhood Trauma Questionnaire, Deshumanization Measure within Romantic Relationships scale, self-esteem scale, violentometer) and an implicit association test (IAT). This second part will last 30 minutes.
Then, the participation of the patient in the study is over.
Eligibility
Primary outcome measure(s)
- Assessment of the correlation between the process of personal dehumanization in victims of domestic violence and their hesitation to file a complaint against the aggressor partner. — 1 year
To assess the correlation between the process of personal dehumanization in victims of domestic violence and their reluctance to file a complaint against the aggressor partner. This assessment will be based specifically on measuring the time, in number of days, elapsed between the start of the violence and the filing of a complaint.
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| CH Henri Laborit | Poitiers | Vienne (86) | Active Not Recruiting |
| CHU Poitiers | Poitiers | Vienne (86) | Recruiting |
More Centre Hospitalier Henri Laborit trials in France
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07015502 on ClinicalTrials.gov ↗ ← All trials in France