Self-Dehumanization and Hesitation to Report Domestic Violence
NCT ID: NCT07015502
Last Updated: 2025-06-11
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
84 participants
OBSERVATIONAL
2024-12-20
2025-12-19
Brief Summary
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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.
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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Questionnaires
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).
Interventions
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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).
Eligibility Criteria
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Inclusion Criteria
* Victim of physical and/or psychological domestic violence taken into care for this reason, following an initial complaint
* Understanding and speaking French
* Subject affiliated to a social security scheme
Exclusion Criteria
* Presence of a disabling mental or cognitive disorder
* Patient employed by the investigator
18 Years
FEMALE
No
Sponsors
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Centre Hospitalier Henri Laborit
OTHER
Responsible Party
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Locations
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CH Henri Laborit
Poitiers, Vienne (86), France
CHU Poitiers
Poitiers, Vienne (86), France
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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2024-A01198-39
Identifier Type: -
Identifier Source: org_study_id
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