Active — Not RecruitingNot Applicable

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

United States200 participantsStarted 2024-01-10

Plain-language 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.

Who can participate

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

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

Timeframe: up to 3 months post visit 1

Trial details

NCT IDNCT06071299

SponsorYale University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-02-15

View on ClinicalTrials.gov More Intimate Partner Violence trials