Actively Recruiting
Identifying Intimate Partner Violence Using a Standardized Questionnaire and Virtual Patients in Primary Care Settings
Led by Region Stockholm · Updated on 2024-04-29
200
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
Sponsors
R
Region Stockholm
Lead Sponsor
L
Linkoeping University
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating three different methods to help primary care professionals better identify individuals exposed to intimate partner violence (IPV) in healthcare settings. The study aims to find out how much each method—a standardized questionnaire, virtual patient training, or a combination of both—helps in detecting potential victims of IPV. It also explores which method healthcare providers find most effective in improving their ability to recognize and respond to IPV cases. The study involves three groups of healthcare professionals at primary care units such as health centers, midwifery clinics, and youth clinics. One group will use a standardized questionnaire to ask patients about exposure to violence over the past year. Another group will receive training through interactive virtual patient scenarios to practice asking about violence and providing appropriate care. The third group will combine both approaches, using the questionnaire and virtual patient training simultaneously over a two-month period. Participants' performance in identifying IPV will be measured before and after the interventions using registry data and protocols from the care units. Additional qualitative focus group interviews with healthcare professionals will gather their views on which intervention was most helpful. The study includes background data collection on the participants, and results will be analyzed to compare the effectiveness of the three methods in increasing IPV identification rates. The project is expected to last three years with ongoing data collection and analysis.
CONDITIONS
Brief 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
- Includes midwives, medical doctors, psychologists, social workers, nurses, and similar healthcare professionals
You will not qualify if you...
- Health care staff who do not want to participate
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 2 months
Participants undergo training and/or administer questionnaires to identify exposure to intimate partner violence over a 2-month period.
Training sessions and questionnaire administration during routine patient visits over 2 months
Duration - Up to 3 years
Researchers collect and analyze registry data and conduct focus group interviews with healthcare professionals to evaluate the effectiveness of the interventions.
Focus group interviews conducted after intervention period
Trial Site Locations
Total: 1 location
1
Linköping University
Linköping, Sweden, 581 83
Actively Recruiting
Research Team
M
Mia Barimani, Professor
W
Wibke Jonas, Ass Prof
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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