Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06322251

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

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
  • Includes midwives, medical doctors, psychologists, social workers, nurses, and similar healthcare professionals
Not Eligible

You will not qualify if you...

  • Health care staff who do not want to participate

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Behavioral Intervention

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

Follow-up and Data Collection

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

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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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