Intimate partner violence: protocol of a quasi-experimental study to increase primary care professionals' ability to identify exposed individuals.
Wibke Jonas, Karin Dahlström, Ragnhild Eikemo...
https://pubmed.ncbi.nlm.nih.gov/42192620/Actively Recruiting
Led by Region Stockholm · Updated on 2024-04-29
200
Participants Needed
1
Research Sites
52 weeks
Total Duration
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 methoda standardized questionnaire, virtual patient training, or a combination of bothhelps 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
Identification of Interpesonal Violence
M
Mia Barimani, Professor
W
Wibke Jonas, Ass Prof
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Region Stockholm
Lead Sponsor
Linkoeping University
Collaborating Sponsor
You may qualify if you...
You will not qualify if you...
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
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
3
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Wibke Jonas, Karin Dahlström, Ragnhild Eikemo...
https://pubmed.ncbi.nlm.nih.gov/42192620/Region Stockholm
Lead Sponsor
Linkoeping University
Collaborating Sponsor