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Behavioral Intervention

F4C for Domestic Violence

N/A

Waitlist Available

Led By Carla Stover, PhD

Research Sponsored by Yale University

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Be older than 18 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up 18 weeks

Awards & highlights

Study Summary

This trial will test a new intervention for fathers who have a history of family violence, compared to a standard program for batterers.

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ 18 weeks

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~18 weeks

This trial's timeline: 3 weeks for screening, Varies for treatment, and 18 weeks for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.

Primary outcome measures

Client Satisfaction Sum Score

Completion Rate

Working Alliance Inventory Sum Score

Secondary outcome measures

Child Maltreatment

Emotional Regulation

Intimate Partner Violence

+1 more

Trial Design

2Treatment groups

Experimental Treatment

Active Control

Group I: F4CExperimental Treatment1 Intervention

Participants randomized to the Fathers for Change (F4C) program.

Group II: BIPActive Control1 Intervention

Participants randomized to the Batterer Intervention Program (BIP).

Treatment

First Studied

Drug Approval Stage

How many patients have taken this drug

F4C

2020

N/A

~60

Do I qualify?Apply below to find out

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Who is running the clinical trial?

Yale UniversityLead Sponsor

1,847 Previous Clinical Trials

2,736,468 Total Patients Enrolled

Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)NIH

1,963 Previous Clinical Trials

2,674,681 Total Patients Enrolled

Carla Stover, PhDPrincipal InvestigatorAssociate Professor at the Yale University School of Medicine Child Study Center

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

What are the objectives of this investigation?

"This 18-week study's primary objective is assessing completion rate. Other secondary objectives include measuring the frequency of child maltreatment with TimeLine Follow-back, analysing emotional regulation through Difficulties in Emotion Regulation Scale (DERS), and investigating reflective functioning via Parent Development Interview-Revised (PDI). To gain additional insight, interviews will be audio recorded and transcribed for further analysis."

Answered by AI

Are there any available enrollment slots in this clinical experiment?

"This experiment, as reported on clinicaltrials.gov is actively seeking participants; it was initially published on September 1st 2020 and the information has been recently edited on October 27th 2022."

Answered by AI

How many participants are currently accepted into this research project?

"Affirmative, the details on clinicaltrials.gov demonstrate that this particular medical trial is presently recruiting participants. It was initiated on September 1st 2020 and has been modified as recently as October 27th 2022. The study requires at least 60 individuals from a single centre to participate."

Answered by AI

Recent research and studies

clinicaltrials.govStudy

Comparing a Fatherhood Focused Individual Intervention to Batterer Intervention to Reduce IPV and Child Maltreatment

2020. "Comparing a Fatherhood Focused Individual Intervention to Batterer Intervention to Reduce IPV and Child Maltreatment". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT04165291.