Identification of Interpesonal Violence

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorRegion Stockholm

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

All health care staff who meet patients at the included study sites are elegible for the study

Midwives, MDs, psychologists, social workers, nurses etc.

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Use of instrument to identify exposure to violence in close relationships

    Behavioral

    Use of instrument to identify exposure to violence in close relationships

Treatment groups

200 Participants
are divided into 3 treatment groups
Group A: Use of questionnaireOther 1 intervention
Group B: Use of virtual patientOther 1 intervention
Group C: Combined use of questionnaire and virtual patientOther 1 intervention

Trial outcomes

Primary outcomes

1

Number of identified persons seeking healthcare who have been exposed to violence

Comparison between before and after intervention - Effectiveness within intervention

Time frame
Baseline

Secondary outcomes

1

Number of identified persons seeking healthcae who have been exposed to violence

Comparison between different interventions (Effectiveness between interventions)

Time frame
After the intervention during a period of 2 months

Other outcomes

1

Experiences of health care staff

Experiences of health care staff to use questionnaire / virtual patient will be obtained in interviews.

Time frame
Three months after the intervention

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Region Stockholm

Lead sponsor

Linkoeping University

Collaborator

Karolinska Institutet

Collaborator

Stockholm University

Collaborator