Intimate Partner Violence Clinical Trial
Official title:
Comparing a Fatherhood Focused Individual Intervention to Batterer Intervention to Reduce IPV and Child Maltreatment
Verified date | March 2024 |
Source | Yale University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
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.
Status | Completed |
Enrollment | 60 |
Est. completion date | August 30, 2023 |
Est. primary completion date | July 30, 2023 |
Accepts healthy volunteers | No |
Gender | Male |
Age group | 18 Years and older |
Eligibility | 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. |
Country | Name | City | State |
---|---|---|---|
United States | Carla Stover | Hamden | Connecticut |
Lead Sponsor | Collaborator |
---|---|
Yale University | Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Completion Rate | To test the hypothesis that fathers randomized to F4C will have higher completion rates than those in the individual BIP treatment, chi-square analysis will be used to examine between group differences in treatment completion. | 18 weeks | |
Primary | Working Alliance Inventory Sum Score | To test the hypothesis that fathers randomized to F4C will report greater overall working alliance, analysis of variance will be used to test between group difference in overall working alliance between F4C and BIP at week 8 of intervention (approximately mid-point). The Working Alliance Inventory (WAI-therapist version) will be used to measure working alliance among clinicians and clients. The WAI for therapists measures the strength of the working alliance with the client with 36 items utilizing a 5-point Likert scale. The minimum score is 0, the maximum score is 180. Higher sum score indicates a stronger working alliance. | 8 weeks | |
Primary | Client Satisfaction Sum Score | To test the hypothesis that fathers randomized to F4C will report greater overall satisfaction, analysis of variance will be used to test between group difference in overall client satisfaction between F4C and BIP. Satisfaction scores range from 2 to 8 with 8 indicating greater overall satisfaction with the services received. | 18 weeks | |
Secondary | Reflective Functioning | Reflective functioning will be assessed using the Parent Development Interview-Revised (PDI). The PDI is a 40-item semi-structured interview that assesses reflective functioning through questions about child-rearing and the ways respondents are like or unlike their own parents. Interviews will be audio recorded and transcribed verbatim for scoring. Interviews are coded on a scale of 1 to 9 with 1 being poor and 9 being excellent reflective functioning. A score of 3 or less is considered very poor. | Baseline and 18 weeks | |
Secondary | Emotional Regulation | Emotional regulation will be assessed with the Difficulties in Emotion Regulation Scale-short form (DERS-SF). The DERS-SF is an 18-item self-report measure scored on a 5-point Likert-type scale where higher scores indicate greater difficulty in emotional regulation. Scores range from 18-90. | Baseline and 18 weeks | |
Secondary | Intimate Partner Violence | The TimeLine Follow-back-Spousal Violence will be used to characterize the frequency of intimate partner violence. | 18 weeks | |
Secondary | Child Maltreatment | Child maltreatment risk will be assessed using TimeLine Follow-back to assess the frequency of behaviors characterized as child maltreatment. | 18 weeks |
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