- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03069898
TRUE Dads: Evaluation of an Intervention Focusing on Father Involvement, Co-parenting, and Employment
Evaluation of the TRUE Dads Intervention
Study Overview
Detailed Description
Interventions to strengthen men's roles as providers, as fathers, and as co-parents have typically been addressed in separate intervention and research silos. The TRUE Dads program proposes a unique integration of employment, fathering, and co-parenting services, with the overarching goal of strengthening fathers and the family unit by: 1) increasing fathers' economic stability and self-sufficiency, 2) enhancing the quantity and quality of father's engagement with their children, 3) improving the quality of the collaborative relationship between fathers and mothers or men and their co-parenting partners, 4) improving the relationship quality of fathers in their intimate partner relationships (with the co-parent or new partner), and 5) positively affecting children's behavior and development.
Twelve hundred fathers will be recruited for the study. After an initial interview of the fathers and their co-parenting partners, who will complete Baseline survey, 720 of the 1,200 fathers and co-parents will be assigned to the TRUE Dads intervention (Program track), and 480 to a no-treatment control condition (Study track). Participants will be informed that the program consists of participation in a series of 12 three-hour meetings. Those 12 sessions include six meetings covering a core fatherhood curriculum, attended with the co-parent, combined with one of three intensives selected by the father: a) six sessions with an emphasis on employment, b) six sessions with an emphasis on building healthy romantic relationships with the co-parent, or c) six sessions with an emphasis on parenting with a participating co-parent. Participants in the Program track may be referred for additional employment, mental health, or other needed services. Both program and control participants (fathers and co-parents) will fill out a Follow-up survey one year from their entrances into the study.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Oklahoma
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Oklahoma City, Oklahoma, United States, 73104
- It's My Community Initiative
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion criteria:
This study begins with a focus on fathers. We are initially recruiting men who:
- Are 18 or older
- Are residing in Oklahoma County/Metro
- Are expecting a child or already have a child age (0-12), with an emphasis on 0-6,
- Have spent time with the child the prior month (or with mother if expecting)
- Are English-speaking. Have not previously participated in the Family Expectations program offered by Public Strategies (Oklahoma) in the last 3 years
Exclusion criteria:
Because this an intervention for fathers that attempts to improve the relationship with the fathers' co-parent, we are accepting fathers only if the co-parent agrees to attend at least the first 6 workshops. In pilot trials, almost all the co-parents are women (wives, intimate partners, grandmothers), but a few are men (the fathers' father, brother, intimate partner)
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Exclusion Criteria:
- Either or both partners have taken part in the Family Expectations project during the past three years, located in the same building, run by Public Strategies
Study Plan
How is the study designed?
Design Details
- Primary Purpose: PREVENTION
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: NONE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
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EXPERIMENTAL: TRUE Dads program track
In the TRUE Dads program, fathers and co-parents begin with a Core workshop meeting weekly for 6 weeks.
After a check-in, a male-female group leader team focuses on a single topic that represents one of the three main goals of the project as a whole: Co-parenting relationships, Parenting, or Employment and financial stability.
From 10 to 18 couples, seated at small tables in a large room, hear mini-lectures, watch videos, and engage in interactive exercises.
Fathers then choose to attend one of three intensive workshops focused on couple relationships OR parenting OR economic self-sufficiency meeting 3 hours per week for the next 6 weeks.
On an as-needed basis, fathers may be referred for employment programs and fathers and co-parents may be referred for mental health or other services.
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The TRUE Dads intervention consists of a set of 12 3-hour workshops that focus on enhancing fathers' role as co-parent, parent, and provider
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NO_INTERVENTION: Control condition study track
Participants (fathers and co-parents) complete intake interview and fill out Baseline survey.
They fill out follow-up survey one year later
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Father/Co-parent relationship quality
Time Frame: Change or maintenance of positive behavior relative to the control group will be assessed at Baseline and 1 year post Baseline.
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This outcome will be measured by a composite of self-report survey items filled out by fathers and co-parents, assessing perceptions of co-parent relationship quality, communication and conflict management abilities.
High scores indicate relationship distress.
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Change or maintenance of positive behavior relative to the control group will be assessed at Baseline and 1 year post Baseline.
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Father involvement
Time Frame: Change or maintenance of positive behavior relative to the control group will be assessed at Baseline and 1 year post Baseline.
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This outcome will be measured by a composite of self-report survey items filled out by both fathers and co-parents, assessing fathers' involvement in childcare tasks, time spent in specific activities with target child, parenting styles, and parenting behaviors.
High scores indicate positive father involvement
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Change or maintenance of positive behavior relative to the control group will be assessed at Baseline and 1 year post Baseline.
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Child well-being
Time Frame: Change or maintenance of positive behavior relative to the control group will be assessed at Baseline and 1 year post Baseline.
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This outcome will be measured by a composite of self-report survey items filled out by fathers and co-parents, assessing child temperament, externalizing behavior problems (aggression, hyperactivity) and internalizing behavior problems (anxiety, depression, shy/withdrawn behavior).
High scores indicate more behavior problems.
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Change or maintenance of positive behavior relative to the control group will be assessed at Baseline and 1 year post Baseline.
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Economic Self-sufficiency
Time Frame: Change or maintenance of positive behavior relative to the control group will be assessed at Baseline and 1 year post Baseline.
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This outcome will be measured by a composite of self-report survey items filled out by fathers and co-parents, assessing employment status, income, behaviors to find a job or acquire new job skills.
High scores indicate more positive economic achievements and more positive attitudes
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Change or maintenance of positive behavior relative to the control group will be assessed at Baseline and 1 year post Baseline.
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Parents adjustment and distress
Time Frame: change or maintenance of positive behavior relative to the control group will be assessed at Baseline and 1 year post Baseline.
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This outcome will be measured by a composite of self-report measures of symptoms of depression (Center for Epidemiological Studies in Depression, CES-D) and anxiety (from the Brief Symptom Inventory).
High scores indicate personal distress.
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change or maintenance of positive behavior relative to the control group will be assessed at Baseline and 1 year post Baseline.
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Philip A. Cowan, PhD, It's My Community Initiative
Publications and helpful links
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 2016-08-9047
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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