Severe Women Injury Factors Test (SWIFT) (SWIFT)

March 4, 2022 updated by: Centre Hospitalier Régional d'Orléans

Descriptive Factors of Intimate Partner Violence on Women Related to "Incapacité Totale de Travail" : Multicenter Prospective Study

Intimate partner violence is a real public health problem, and affects all socio-cultural backgrounds It is defined by behavior within an intimate relationship that causes physical, psychological or sexual harm or suffering to the people in that relationship.

Several risk factors exist such as young age, low level of education, exposing to violence during childhood, pregnancy or addictions.

Study Overview

Status

Terminated

Conditions

Intervention / Treatment

Detailed Description

Routine screening is recommended with redaction of medical certificate in which doctor have to determine l'"Incapacité Totale de Travail" corresponding to the duration of discomfort (physical and psychological repercussions) in the activities of daily life.

It is a legal notion allows to rule on the responsibility of the author. The sentence is increased if the ITT is greater than 8 days.

Worldwide, 30% of women suffered violence whose most common form is intimate partner violence, but legal proceedings have been initiated in less than 25% of the cases.

The trauma of women victims of domestic violence worsens with the repetitions of assaults.

The investigators suppose that the duration of ITT is an indicator of the severity of the injuries sustained.

So, the investigators want to highlight the socio-demographic characteristics and describe the spouse abuse, and then related theese factors to " Incapacité Totale de Travail " (term used in law. It is a scale for assessing the importance of injuries).

Study Type

Observational

Enrollment (Actual)

60

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Orléans, France, 45067
        • Regional Hospital center of ORLEANS
      • Orléans, France
        • Centre Hospitalier Régional d'Orléans (UMJ)
      • Tours, France
        • CHRU de Tours (SAU)
      • Tours, France
        • CHRU de Tours (UMJ)
      • Tours, France
        • SOS Médecins Tours

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Sampling Method

Non-Probability Sample

Study Population

Adult women consulting a doctor for intimate partner violence

Description

Inclusion Criteria:

  • Adult patients
  • Admission to emergency for intimate partner violence
  • Or consultation to SOS doctor for intimate partner violence
  • Or consultation to medico-judicial unit for intimate partner violence
  • No verbal opposition to inclusion

Exclusion Criteria:

  • Non intimate partner violence
  • Patient under guardianship or curatorship
  • Non French speaker
  • Coma or inability to express non-opposition
  • Prior participation in another center

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Women consulting for spouse abuse
The study focuses on women consulting a doctor as part of spouse abuse, whatever the context (at the request of the police or not) or their motivation (medical or social).
It is a survey that the patient and doctor must complete.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Descriptive factors of intimate partner violence on women related to "Incapacité Totale de Travail"
Time Frame: Month 24
Highlight the socio-demographic characteristics and the violence suffered by women victims of intimate partner violence, and related this factors to " Incapacité Totale de travail "
Month 24

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Descriptive factors of intimate partner violence on women related to "Incapacité Totale de travail" for more than eight days.
Time Frame: Month 24
Highlight the socio-demographic characteristics and the violence suffered by women victims of intimate partner violence, and related this factors to an " Incapacité Totale de travail " for more than eight days.
Month 24
Spontaneus request of a medical certificate during the consultation.
Time Frame: Month 24
Determine the proportion of women asking for a medical certificate during the consultation.
Month 24

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Julien PASSERIEUX, Dr, Chr D'Orleans

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 8, 2021

Primary Completion (Actual)

July 23, 2021

Study Completion (Actual)

July 23, 2021

Study Registration Dates

First Submitted

March 31, 2021

First Submitted That Met QC Criteria

March 31, 2021

First Posted (Actual)

April 2, 2021

Study Record Updates

Last Update Posted (Actual)

March 21, 2022

Last Update Submitted That Met QC Criteria

March 4, 2022

Last Verified

March 1, 2022

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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