Actively Recruiting
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
Eligibility Criteria
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.
You will not qualify if you...
- Health care staff who does not want to participate
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Linköping University
Linköping, Sweden, 581 83
Actively Recruiting
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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