Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT06322251

Identification of Interpesonal Violence

Led by Region Stockholm · Updated on 2024-04-29

200

Participants Needed

1

Research Sites

221 weeks

Total Duration

On this page

Sponsors

R

Region Stockholm

Lead Sponsor

L

Linkoeping University

Collaborating Sponsor

AI-Summary

What this Trial Is About

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

Official Title

Identification of Interpesonal Violence

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • All health care staff who meet patients at the included study sites are eligible for the study
  • Midwives, MDs, psychologists, social workers, nurses, etc.
Not Eligible

You will not qualify if you...

  • Health care staff who does not want to participate

AI-Screening

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Trial Site Locations

Total: 1 location

1

Linköping University

Linköping, Sweden, 581 83

Actively Recruiting

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Research Team

M

Mia Barimani, Professor

CONTACT

W

Wibke Jonas, Ass Prof

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

HEALTH_SERVICES_RESEARCH

Number of Arms

3

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