Growing Responsible Fathers Descriptive Program Evaluation

January 4, 2024 updated by: Jeff Will, University of North Florida
The overall evaluation plan for the Growing Responsible Fathers program (Fatherhood PRIDE) will utilize both a process evaluation and an outcomes evaluation, and will include both quantitative and qualitative approaches. Pre- and post-test surveys will be used to measure short-term outcomes outlined in the logic model including whether or not there has been an increase in self-efficacy and knowledge related to personal finance, parent engagement, healthy relationships, and education. Pre-test surveys will be administered at intake and/or prior to program activity and post-test surveys will be conducted at the conclusion of the program activity.

Study Overview

Status

Completed

Detailed Description

The overall evaluation plan for the Growing Responsible Fathers program (Fatherhood PRIDE) will utilize both a process evaluation and an outcomes evaluation, and will include both quantitative and qualitative approaches. Pre- and post-test surveys will be used to measure short-term outcomes outlined in the logic model including whether or not there has been an increase in self-efficacy and knowledge related to personal finance, parent engagement, healthy relationships, and education. Pre-test surveys will be administered at intake and/or prior to program activity and post-test surveys will be conducted at the conclusion of the program activity.

Intermediate outcomes will be measured using a follow-up survey at six (6) months after completing the primary components of the program. The follow-up surveys will be administered via a variety of methods in order to increase response rates and will measure outcomes identified in the logic model such as knowledge and self-efficacy.

Additional attempts will be made online through an email invitation as well as with phone calls. Center for Community Initiatives staff will be responsible for conducting the follow-up surveys with the program participants. Focus groups will be conducted with a volunteer sample of participants at the end of their program workshops to assess satisfaction with the program, what worked, and what could be improved.

Study Type

Observational

Enrollment (Actual)

1350

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

16 years and older (Child, Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

The program will serve 1350 fathers in Baker, Clay, Duval, Nassau and St. Johns' counties in the five year project period. Fathers are referred by the local family courts, re-entry centers and the federal and state Healthy Start programs; the child welfare system; and other community partners. The program serves two sub-populations: incarcerated fathers and community fathers.

Description

Inclusion Criteria:

  • Fathers or father figure

Exclusion Criteria:

-

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Community
Community fathers include fathers who are recruited through community partners and self-referrals. Only fathers 18 years of age and older are included in program analysis
24 hours of fatherhood curriculum, 6 hours of financial literacy, workforce development, and case management.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Increased knowledge gain
Time Frame: post test after 12 week program (incarcerated) or 4-6 weeks (community)
Do participants who complete the program increase knowledge gains in financial literacy, co-parenting skills, and responsible fatherhood/family relationships after participating in program as measured by pre/post test. The outcome measure for each domain (financial literacy, co-parenting skills, and responsible fatherhood/family relationships) will be a total calculated from the number of correctly answered questions adapted from the curriculum.
post test after 12 week program (incarcerated) or 4-6 weeks (community)
Increased self-efficacy
Time Frame: Post test after 4-6 week program (community)
Do Community participants who complete the program increase self-efficacy to pay for child support as measured by pre/post test. The outcome measure will be a total of six scores (range 0-100) to statements related to paying child support.
Post test after 4-6 week program (community)
Increased engagement
Time Frame: Post test after 4-6 week program (community) and 6 month followup survey
Do Community Participants who complete the program increase self reported engagement with their children as measured by pre/post test. The outcome measure will be a total of six scores (range 0-4) of various engagement activities with youngest child. These engagement measures were adapted from the FRPN Father Engagement Scale.
Post test after 4-6 week program (community) and 6 month followup survey

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Jeff Will, University of North Florida

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)

June 1, 2016

Primary Completion (Actual)

September 1, 2020

Study Completion (Actual)

December 1, 2020

Study Registration Dates

First Submitted

October 2, 2018

First Submitted That Met QC Criteria

May 22, 2019

First Posted (Actual)

May 24, 2019

Study Record Updates

Last Update Posted (Estimated)

January 8, 2024

Last Update Submitted That Met QC Criteria

January 4, 2024

Last Verified

March 1, 2020

More Information

Terms related to this study

Other Study ID Numbers

  • 16-012

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

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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