NCT07015502

Brief 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.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
84

participants targeted

Target at P50-P75 for all trials

Timeline
Completed

Started Dec 2024

Shorter than P25 for all trials

Geographic Reach
1 country

2 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

December 20, 2024

Completed
6 months until next milestone

First Submitted

Initial submission to the registry

June 3, 2025

Completed
8 days until next milestone

First Posted

Study publicly available on registry

June 11, 2025

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 19, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 19, 2025

Completed
Last Updated

June 11, 2025

Status Verified

June 1, 2025

Enrollment Period

12 months

First QC Date

June 3, 2025

Last Update Submit

June 3, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • 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.

    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.

    1 year

Study Arms (1)

Questionnaires

Other: Questionnaires

Interventions

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).

Questionnaires

Eligibility Criteria

Age18 Years+
Sexfemale
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

women victims of domestic violence

You may qualify if:

  • Woman over 18
  • 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

You may not qualify if:

  • Patient under legal protection measure (guardianship or legal protection)
  • Presence of a disabling mental or cognitive disorder
  • Patient employed by the investigator

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

CH Henri Laborit

Poitiers, Vienne (86), 86000, France

ACTIVE NOT RECRUITING

CHU Poitiers

Poitiers, Vienne (86), 86000, France

RECRUITING

MeSH Terms

Interventions

Surveys and Questionnaires

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Central Study Contacts

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

June 3, 2025

First Posted

June 11, 2025

Study Start

December 20, 2024

Primary Completion

December 19, 2025

Study Completion

December 19, 2025

Last Updated

June 11, 2025

Record last verified: 2025-06

Data Sharing

IPD Sharing
Will not share

Locations