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Clinical Trials/NCT06071299
NCT06071299
Active, Not Recruiting
N/A

Impact of Family-Centered Care for Intimate Partner Violence (IPV)

Yale University2 sites in 1 country200 target enrollmentJanuary 10, 2024

Overview

Phase
N/A
Intervention
Not specified
Conditions
Intimate Partner Violence
Sponsor
Yale University
Enrollment
200
Locations
2
Primary Endpoint
Percentage of caregivers with follow-up visits with an IPV advocate
Status
Active, Not Recruiting
Last Updated
4 months ago

Overview

Brief Summary

The purpose of the study will be to determine how participation in Family-Centered Care (FCC) compared to Child-centered care (CCC) will affect caregiver engagement in IPV-based community services, caregiver perceptions of empowerment and survivor-defined practice, and clinical outcomes for children exposed to IPV.

Detailed Description

The study population includes victims of intimate partner violence whose children \< 5-years old have been referred to Child Protective Services due to exposure to IPV and who have agreed to a medical evaluation for the child(ren) in the child advocacy center or the SCAN clinic and don't already have a connection to an IPV advocate. The study population will include adults who are primarily English or Spanish Language preferring. For professionals, the target audience will be local CPS investigators in the New Haven and Hartford CPS office, IPV advocates at the New Haven Umbrella Center for Intimate Partner Violence Services and The Hartford Interval House and child abuse pediatricians at Yale University School of Medicine and at the Connecticut Childrens Medical Center.

Registry
clinicaltrials.gov
Start Date
January 10, 2024
End Date
December 15, 2026
Last Updated
4 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Have a child \< 5-years-old who been reported to Child Protectives Services for IPV exposure
  • Parent \> 18 years old who has agreed to a medical evaluation for the child at the child advocacy center
  • Does not already have a connection to an IPV advocate
  • Able to speak English or Spanish fluently
  • Not a ward of department of children and families

Exclusion Criteria

  • Ward of the state
  • Language preference other than English or Spanish

Outcomes

Primary Outcomes

Percentage of caregivers with follow-up visits with an IPV advocate

Time Frame: up to 3 months post visit 1

Percentage of caregivers who have at least one follow-up visit with an IPV advocate by 3 months after the initial visit by self-report.

Secondary Outcomes

  • Percentage of evaluated children who complete a skeletal survey(up to 4 weeks post visit 1)
  • Perceptions of survivor-defined practice using the Survivor Defined Practice Scale (SDPS)(up to 4 weeks post visit 1)
  • Frequency of IPV-related episodes assessed using the Psychological Maltreatment of Women Inventory (PMWI)- Short form(up to 1 year post visit 1, until child is 2 years of age)
  • Perceptions of safety-related empowerment using the Measure of Victim Empowerment Related to Safety (MOVERS) scale.(up to 4 weeks post visit 1)
  • Frequency of IPV-related episodes assessed using the Conflict Tactic Scale 2 (CTS2) for partner's behaviors(up to 1 year post visit 1, until child is 2 years of age)
  • Number of reports to Child Protective Services (CPS) for IPV(up to 1 year post visit 1)

Study Sites (2)

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