Local Evaluation of the Saint Francis Ministries Fatherhood FIRE Program

March 31, 2025 updated by: University of Kansas

KS, NE, and TX Fathers, Couples, and Co-parents Whose Children Are Involved in the Child Welfare System Will Gain the Skills and Knowledge to be Better Parents Through Saint Francis Fatherhood FIRE

This study is the local process and impact evaluation for Saint Francis Ministries' Fatherhood FIRE Program.

Study Overview

Detailed Description

This project is based on federal legislation that requires evaluation of a program being implemented and delivered by Saint Francis Ministries, a community-based non-profit organization serving children and families. Saint Francis Ministries received federal funds to expand and deliver the Fatherhood FIRE Program to community-based and justice-system involved fathers in their service area. The FIRE program, which stands for Family-Oriented, Interconnected, Resilient, and Essential, aims to promote responsible and positive fatherhood parenting practices and develop and maintain healthy relationships with their partners and other co-parents (e.g., mothers of their children). Evaluation of the program is a condition of Saint Francis Ministries' grant award from the U.S. Department of Health and Human Services. The KU evaluation team at the School of Social Welfare has been contracted by Saint Francis Ministries to conduct the evaluation. The evaluation will be carried out in two parts: 1) a process evaluation and 2 an outcomes evaluation. The process and target populations for both the process and outcomes components are as follows. PROCESS EVALUATION: The process study involves individuals involved in the implementation of the Fatherhood FIRE program at Saint Francis Ministries. Specific populations eligible for inclusion in the process evaluation include: (1) implementation teams facilitating the Fatherhood FIRE program in three states in Saint Francis Ministries service area (Kansas, Nebraska, & Texas), (2) members of the Fatherhood FIRE Data, Assessment, and Dissemination Workgroup, an advisory group comprised of Saint Francis program administrators and the evaluation team charged with planning and overseeing data collection, evaluation, and dissemination efforts, and (3) the evaluation study team. OUTCOMES EVALUATION: Fathers ages 18 and older who are not incarcerated and are enrolled and participating in the Fatherhood FIRE program. To be eligible for inclusion in the evaluation study, program participants must not be incarcerated, have children up to age 24, and may be living with or apart from their children. Eligible participants may be biological parents, adoptive or foster parents, or other caregivers in the parenting role if they have children who meet the age criteria.

Study Type

Interventional

Enrollment (Estimated)

600

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Kansas
      • Lawrence, Kansas, United States, 66045
        • University of Kansas School of Social Welfare

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Fathers with children up to 24 year old
  • Fathers participating in the Saint Francis Fatherhood FIRE Program

Exclusion Criteria:

  • Fathers who are incarcerated

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Enhanced Treatment Group
Randomized group of participants receiving an enhanced Fatherhood FIRE program.
Fathers receive an enhanced series of pro-parenting, relationship, and economic stability workshops over 16 weeks. Workshop series are based on a diverse curricula including a combination of either 24/7 Dad or Parent Project and Connections to Success and the Nurturing Fathers enhancement program.
Active Comparator: Control Group
Randomized group of participants receiving the 'services as usual' Fatherhood program.
Fathers receive the services as usual approach which includes a series of pro-parenting, relationship, and economic stability workshops over 13 weeks. Workshop series are based on a diverse curricula including a combination of either 24/7 Dad or Parent Project and Connections to Success.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Healthy relationship and marriage skills
Time Frame: Measurement of the outcome will occur at three-time points: 1) Pre intervention, 2) at program completion an average of 16 weeks after pre-intervention measure, 3) 3-months post program completion
Dads in the enhanced group demonstrate larger and more sustained change in healthy relationship and marriage skills (e.g., compromise and interactional reactivity) than the control group. The measurement tool used to assess this outcome is the Romantic Partner Conflict Scale (Zacchilli, Hendrick, & Hendrick, 2009).
Measurement of the outcome will occur at three-time points: 1) Pre intervention, 2) at program completion an average of 16 weeks after pre-intervention measure, 3) 3-months post program completion
Parenting skills
Time Frame: Measurement of the outcome will occur at three-time points: 1) Pre intervention, 2) at program completion an average of 16 weeks after pre-intervention measure, 3) 3-months post program completion
Dads in the enhanced group demonstrate larger and more sustained change in parenting skills than the control group. The measurement tool used to assess this outcome is the Parenting Sense of Competence Scale (Ohan, Leung, & Jonston, 2000; Johnston & Mash, 1989; Gillmore & Cuskelly, 2008).
Measurement of the outcome will occur at three-time points: 1) Pre intervention, 2) at program completion an average of 16 weeks after pre-intervention measure, 3) 3-months post program completion
Co-parenting skills
Time Frame: Measurement of the outcome will occur at three-time points: 1) Pre intervention, 2) at program completion an average of 16 weeks after pre-intervention measure, 3) 3-months post program completion
Dads in the enhanced group demonstrate larger and more sustained change in co-parenting skills than the control group. The measurement tool used to assess this outcome is the Daily Co-Parenting Scale (D-COP; McDaniel, Teti, & Feinberg, 2017).
Measurement of the outcome will occur at three-time points: 1) Pre intervention, 2) at program completion an average of 16 weeks after pre-intervention measure, 3) 3-months post program completion
Father-child engagement
Time Frame: Measurement of the outcome will occur at three-time points: 1) Pre intervention, 2) at program completion an average of 16 weeks after pre-intervention measure, 3) 3-months post program completion
Dads in the enhanced group demonstrate larger and more sustained change in father/child engagement than the control group. The measurement tool used to assess this outcome is the Inventory of Father Involvement (Hawkins, Bradford, Palkovitz, & Christiansen, 1999).
Measurement of the outcome will occur at three-time points: 1) Pre intervention, 2) at program completion an average of 16 weeks after pre-intervention measure, 3) 3-months post program completion

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Jared L Barton, PhD, University of Kansas

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 1, 2022

Primary Completion (Estimated)

March 30, 2025

Study Completion (Estimated)

September 30, 2025

Study Registration Dates

First Submitted

October 1, 2021

First Submitted That Met QC Criteria

October 15, 2021

First Posted (Actual)

October 28, 2021

Study Record Updates

Last Update Posted (Actual)

April 3, 2025

Last Update Submitted That Met QC Criteria

March 31, 2025

Last Verified

April 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 146802

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

De-identified data will be archived at the end of the study through an accessible archiving site.

IPD Sharing Time Frame

Data will become available at the end of the study anticipated September 2025

IPD Sharing Supporting Information Type

  • STUDY_PROTOCOL
  • SAP
  • ICF
  • CSR

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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