MedTrace Logo

Identification of Interpesonal Violence

NCT06322251 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2024-04-29

No results posted yet for this study

Summary

The goal of this study is to increase primary care professional's ability to identify individuals exposed to intimate partner violence (IPV) in primary health care settings.

The main questions it aims to answer are

1. To what extent do the following three interventions contribute to identify potential victims of IPV: (1) the use of a standardized questionnaire that screens exposure to IPV, (2) staff using tailored virtual patients for clinical training on IPV and (3) a combination of interventions 1 and 2?
2. Which intervention do primary care professionals experience as most effective in increasing the ability to identify and respond to victims of IPV?

Participants will be divided to apply one of the three interventions in their health care setting: 1) a standardized questionnaire to patients, 2) virtual patients tailored to health professionals, and 3) a combination of 1 and 2.

Pre-and post-measurement of the health professionals identification of patients exposed to IPV will will be used to explore the effect of the interventions.

Focus group interviews with the participating health professionals will be a qualitative complement. The participants will be asked about what intervention they experience as the most effective in increasing the ability to identify victims of IPV.

Conditions

  • Primary Health Care
  • Interpersonal Violence
  • Youth
  • Pregnancy

Interventions

BEHAVIORAL

Use of instrument to identify exposure to violence in close relationships

Use of instrument to identify exposure to violence in close relationships

Sponsors & Collaborators

  • Linkoeping University

    collaborator OTHER_GOV

  • Karolinska Institutet

    collaborator OTHER

  • Stockholm University

    collaborator OTHER

  • Region Stockholm

    lead OTHER_GOV

Principal Investigators

  • Mia M Barimani, Professor · Linkoeping University

Study Design

Allocation
RANDOMIZED
Purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-04-01
Primary Completion
2027-06-30
Completion
2028-06-30

Countries

  • Sweden

Study Locations

More Related Trials

Entities

Companies

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 NCT06322251 on ClinicalTrials.gov