Gentle Warriors Academy Healthy Marriage and Responsible Fatherhood Program Evaluation

October 9, 2025 updated by: Midwest Evaluation & Research

Gentle Warriors Academy Program Evaluation

The purpose of this descriptive study is to explore whether there is an association between participation in the Gentle Warriors Academy and improvements in outcomes related to parenting, co-parenting, and parental well-being. Participants are surveyed at program entry, program exit, and 12 months following program enrollment, and changes in participant attitudes and behaviors are assessed over time.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

This study is a descriptive evaluation of the Gentle Warriors Academy program offered to fathers in the Atlanta metropolitan area. Program participants are informed about the study and asked to provide consent to participate in the evaluation of the program. Consenting participants complete surveys at program enrollment, program exit, and 12 months after program enrollment, and survey data is used to determine if the program is associated with short-term and long-term changes in attitudes and behaviors among participants. Changes in parenting attitudes and parental well-being are assessed by comparing survey answers before and after participating in 26 hours of the Next Level Fatherhood primary curriculum. Changes in behaviors related to parenting and co-parenting are assessed from program entry to 12 months post-enrollment.

Study Type

Interventional

Enrollment (Actual)

731

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

    • Georgia
      • Atlanta, Georgia, United States, 30338
        • Fathers Incorporated

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Adult (age 18 and older)
  • Father/father figure
  • With children under age 16
  • Reside in Metro Atlanta area

Exclusion Criteria:

  • Minor (under the age of 18)
  • Not a father/father figure
  • Children older than 16 years old
  • Reside outside of Metro Atlanta area

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: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Primary Services
Participants receive 26 hours of Next Level Fatherhood curriculum, 2 hours of child maltreatment workshops, 2 hours of anger management workshops, and 2 hours of optional legitimation workshops. Participants also receive ongoing case management and support services.
Participants receive 26 hours of Next Level Fatherhood curriculum, 2 hours of child maltreatment workshops, 2 hours of anger management workshops, and 2 hours of optional legitimation workshops. Participants also receive ongoing case management and support services.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
1) Healthy Parenting Attitudes Measurement #1
Time Frame: baseline and program exit at 10 weeks post-enrollment

Will participants report significantly healthier parenting attitudes after completing primary workshops, as compared to responses at program enrollment?

Items measured include:

Parenting attitudes measured with:

7 items - frequency of feelings about participant's youngest child (categorical, 5-point scale)

Measured on the parenting attitudes scale #1 as:

1 = always, 2 = often, 3 = sometimes, 4 = rarely, 5 = never

The construct is created by adding all 7 scores together and dividing by 7. The higher the score on a scale of 1-5, the better the outcome. The lower the score, the worse the outcome.

Maximum score: 5.0, minimum score: 1.0

baseline and program exit at 10 weeks post-enrollment
2) Healthy Parenting Behaviors Measurement #1
Time Frame: Time frame: change from baseline in parenting behaviors (interactions with child) from enrollment to 1 year post-enrollment.

Will participants report significantly healthier parenting behavior one year after enrolling in the program, as compared to responses at baseline?

Items measured include:

Parenting behavior measured with:

11 items - frequency of key behaviors with participant's youngest child (categorical, 5-point scale)

Measured on the parenting behavior scale #1 as:

1 = never, 2 = 1 to 2 days per month, 3 = 3 or 4 days per month, 4 = 2 or 3 days per week, 5 = every day or almost every day

The higher the rating, the better the score.

The construct is created by adding all 11 scores together and dividing by 11. The higher the score on a scale of 1-5, the better the outcome. The lower the score, the worse the outcome.

maximum score: 5.0, minimum score: 1.0

Time frame: change from baseline in parenting behaviors (interactions with child) from enrollment to 1 year post-enrollment.
3) Healthy Co-parenting Behaviors Measurement #1
Time Frame: change from baseline in co-parenting behaviors (interactions with co-parent) from enrollment to 1 year post-enrollment.

Will participants report significantly healthier co-parenting behavior one year after enrolling in the program, as compared to responses at baseline?

Items measured include:

11 items: frequency of agreement with key co-parenting behaviors (categorical, 5-point scale)

Measured on the co-parenting behavior scale #1 as:

1 = strongly disagree, 2 = disagree, 3 = neutral, 4 = agree, 5 = strongly agree

The construct is created by adding all scores together and dividing by 11. The higher the score on a scale of 1-5, the better the outcome. The lower the score, the worse the outcome.

change from baseline in co-parenting behaviors (interactions with co-parent) from enrollment to 1 year post-enrollment.
4) Parent Wellbeing Measurement #1
Time Frame: change from baseline in parental wellbeing (feelings about parenting) from enrollment to program exit (10 weeks).

Will participants report significantly higher parental wellbeing after completing primary workshops, as compared to responses at program enrollment?

1 item: frequency of feeling overwhelmed by parenting responsibilities (categorical, 4-point scale)

1 = never, 2 = hardly ever, 3 = sometimes, 4 = often

The lower the number, the better the score. Maximum score=4.0, minimum score=1

change from baseline in parental wellbeing (feelings about parenting) from enrollment to program exit (10 weeks).

Collaborators and Investigators

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

Collaborators

Investigators

  • Principal Investigator: Matt D Shepherd, PhD, Midwest Evaluation and Research

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)

April 1, 2021

Primary Completion (Actual)

March 28, 2024

Study Completion (Actual)

August 29, 2025

Study Registration Dates

First Submitted

March 21, 2025

First Submitted That Met QC Criteria

March 21, 2025

First Posted (Actual)

March 27, 2025

Study Record Updates

Last Update Posted (Estimated)

November 5, 2025

Last Update Submitted That Met QC Criteria

October 9, 2025

Last Verified

October 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • #2021/03/42

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

All participant data will be confidential and aggregated. No individual participant data will be released unless requested by the courts. This study looks at data as a whole.

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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