Creating a program to reduce maternal deaths through violence intervention training
Violence Intervention and Prevention (VIP) Corps to Reduce Maternal Injuries and Deaths Due to Violence
This study is testing a new training program for students to help reduce maternal deaths caused by violence by teaching them how to recognize and respond to intimate partner violence.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 2800 (estimated) |
| Ages | 18 Years to 30 Years |
| Sex | All |
| Sponsor | University of Kentucky Academic / other |
| Locations | 1 site (Lexington, Kentucky) |
| Trial ID | NCT06089109 on ClinicalTrials.gov |
What this trial studies
This observational study aims to establish and evaluate a Violence Intervention and Prevention Corps (VIP Corps) training program among undergraduate and professional students at the University of Kentucky. The study will also develop a maternal injury surveillance system (MISS) to enhance an existing maternal violent death registry in Kentucky. By training future health and social service professionals, the study seeks to address and reduce maternal morbidity and mortality rates associated with violence. The effectiveness of the VIP Corps training will be assessed through a randomized controlled trial, focusing on improving knowledge and screening behaviors related to intimate partner violence.
Who should consider this trial
Good fit: Ideal candidates for this study are undergraduate and professional students aged 18-30 enrolled in helping professions programs.
Not a fit: Patients who are not enrolled in helping professions programs or are outside the age range of 18-30 may not benefit from this study.
Why it matters
Potential benefit: If successful, this initiative could significantly lower maternal mortality and morbidity rates linked to violence in Kentucky.
How similar studies have performed: While similar approaches have been explored, this specific intervention and surveillance system is novel and has not been extensively tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Students enrolled in a helping professions program * 18 years of age through 30 years of age * Students whom will have direct interaction with patients or clients that may experience interpersonal violence (IPV) Exclusion Criteria: * Students not enrolled in a helping professions program * Students under age 18 or over age 30 * Students with no direct interaction with patients or clients
Where this trial is running
Lexington, Kentucky
- University of Kentucky — Lexington, Kentucky, United States (Recruiting)
Study contacts
- Principal investigator: Ann L Coker, PhD — University of Kentucky
- Study coordinator: Ann L Coker, PhD
- Email: ann.coker@uky.edu
- Phone: 859-323-0429
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.