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

Status Recruiting

Clinical Trial 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.

Clinical Trial Description

The study population includes victims of intimate partner violence whose children < 3-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. ;

Study Design

Related Conditions & MeSH terms

Intimate Partner Violence

Clinical Trial Details

NCT number	NCT06071299
Study type	Interventional
Source	Yale University
Contact	Gunjan Tiyyagura, MD, MHS
Phone	203-464-6343
Email	gunjan.kamdar@yale.edu
Status	Recruiting
Phase	N/A
Start date	January 10, 2024
Completion date	November 2027

View Details

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