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

Yale University logo

Yale University

Status

Completed

Conditions

Intimate Partner Violence

Treatments

Behavioral: F4C
Behavioral: BIP

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04165291
1R21HD099318-01A1 (U.S. NIH Grant/Contract)
2000026789

Details and patient eligibility

About

This randomized trial will test a newly developed intervention aimed at fathers who have a history of family violence compared to a standard batterer intervention program.

Full description

This study will expand on Fathers for Change (F4C), a novel intervention for fathers with histories of perpetrating intimate partner violence (IPV). F4C is designed to meet a significant unmet intervention need for fathers who have a history of family violence who are not helped by currently available batterer intervention programs (BIPs). BIPs that are currently available nationally have shown limited efficacy with high rates of repeat violence.

This project will provide needed data to further develop F4C and move to a Stage II efficacy trial by: 1) revising the BIP group intervention manual to be delivered in an individual treatment format; 2) develop a fidelity measure for F4C and the BIP; 4) conduct a stage 1b randomized trial (consistent with the stage model of intervention development) to show initial feasibility, acceptability and intervention signal with the targeted population.

Sixty fathers with a history of IPV who have already failed a treatment as usual group BIP will be randomly assigned to F4C or an individually delivered comparable dose of BIP. Reflective functioning and emotion regulation will be examined as the mechanisms through which Fathers for Change reduces IPV and child maltreatment risk behaviors.

Enrollment

60 patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • A reported an incident of IPV (pushing, slapping, kicking) within the last 12 months prior to screening (based on court/police records, partner or self- report);
  • have at least one biological child aged 6 months to 7 years with whom they have contact in person or by phone/facetime etc. at least monthly;
  • are able to complete assessments in English;
  • agree to have their female coparents (mother of the youngest child) contacted as collateral informants and for consent for participation of their shared child.

Exclusion criteria

  • Men who have an active full/no contact protective order pertaining to their child since this will preclude participation in the father-child play assessment (many men will have full no-contact orders with their partners, but it is more common for men to still be allowed at least supervised contact with their children even with a full/no contact order with their partner);
  • physiological addiction to a substance that requires detoxification. Fathers will be evaluated using the Addiction Severity Index and urine toxicology screens. If fathers report difficulties with physiological withdrawal from substances (e.g. delirium tremens, shaking, nausea) they will be referred for detox services. They can be re-evaluated following a detox program with documentation from the detox center of successful completion and clean urine screen.;
  • anyone with a cognitive impairment that will not allow for understanding of the study interventions (a mini mental state score <25);
  • anyone with a current untreated psychotic disorder;
  • anyone currently suicidal or homicidal based on screening using the BSI.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

F4C
Experimental group
Description:
Participants randomized to the Fathers for Change (F4C) program.
Treatment:
Behavioral: F4C
BIP
Active Comparator group
Description:
Participants randomized to the Batterer Intervention Program (BIP).
Treatment:
Behavioral: BIP

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Tami Sullivan, PhD; Carla Stover, PhD

Data sourced from clinicaltrials.gov

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