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Self Defining Memories in Women Victims of Intimate Partner Violence.

NCT03906487 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2020-07-31

No results posted yet for this study

Summary

A recent report by the World Health Organization demonstrated that 30 % of women worldwide have been victims of intimate-partner violence (IPV). IPV is a public health problem thus it seems important to propose relevant care. It is difficult to carry out an effective therapy. Psychological care is based on cognitive abilities but these women have cognitive impairment. Few studies investigated their cognitive dysfunction. Investigators suggest in this study an exploration of the Self Defining Memories (SDM) which can highlight the loss of identity of these women and a new target of therapy.

Conditions

  • Domestic Violence

Interventions

BEHAVIORAL

Assessment measures MINI, PCL5 and BDI-II and definition of 5 SDM

This group will have two visits: * the first to verify inclusion criteria and assessed psychotraumatic and depressive symptoms by completing assessment measures called MINI, PCL-5, BDI-II ; * the last to characterize the SDM by defining 5 personal memories

BEHAVIORAL

Assessment measures MINI and definition of 5 SDM

This group will have two visits: * the first to verify inclusion criteria and assessed psychotraumatic and depressive symptoms by completing MINI questionary; * the last to characterize the SDM by and defining 5 personal memories

Sponsors & Collaborators

  • University Hospital, Toulouse

    lead OTHER

Principal Investigators

  • Damien PIERRE, MD · University Hospital, Toulouse

Study Design

Allocation
NON_RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-02-06
Primary Completion
2021-11-30
Completion
2021-12-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03906487 on ClinicalTrials.gov