FathersNCT06907719

Strong Fathers, Stronger Families Healthy Marriage and Responsible Fatherhood Program Evaluation

A study testing Primary Services in people with Fathers, run by Midwest Evaluation & Research at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record

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Trial summary

The purpose of this descriptive study is to explore whether there is an association between participation in the Strong Fathers, Stronger Families program and improvements in outcomes related to parenting, co-parenting, and economic stability. Read more about this study

Who is it for?: Ages 18 years and older, men onlyHealthy volunteers can take part
Conditions the study is for: Fathers
What is being tested?: Primary Services
Could I receive a placebo?: No, everyone receives an active treatment
How many people: 996 participants
Where: 1 siteUnited States
Study dates: 1 Apr 2021to 29 Aug 2025
Phase: Interventional
Are there results?: Yes, posted in the registrySummary in the doctors' view

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

Ages 18 years and older
Men only
Healthy volunteers accepted
Adult, Older adult

Who may be able to join

Adult (age 18 and older)
With children ages 0-24
Father/father figure
Reside in Memphis metropolitan area

Who cannot join

Minor (under the age of 18)
Not a father/father figure
Children older than 24 years old
Reside outside of Memphis metropolitan area

Trial locations and contacts

1 site in 1 country.

United States1 site

Seedco-Midsouth
Memphis, Tennessee, 38117

Other trials in United States

About this study

Official title: Strong Fathers, Stronger Families Program Evaluation

Read the detailed description

This study is a descriptive evaluation of the Strong Fathers, Stronger Families program offered to fathers in the Memphis metropolitan area. Program participants are informed about the study and asked to provide consent to participate in the evaluation of the ten-week program. Consenting participants complete surveys at program enrollment and program exit, and survey data is used to determine if program participation is associated with short-term changes in attitudes and behaviors among participants. Changes in parenting, co-parenting, and economic stability outcomes are assessed by comparing survey answers before and after participating in 40 hours of the Blueprint and 24/7 Dad curricula.

Conditions: Fathers
Being tested: Primary Services

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Primary ServicesOther
Participants receive 40 hours of the Blueprint and 24/7 Dad curricula over the course of ten weeks.

Study groups in NCT06907719
Study group	Role	What they receive
Primary Services	Experimental	Primary Services Participants receive 40 hours of the Blueprint and 24/7 Dad curricula over the course of ten weeks. Receives: Other: Primary Services

What is being measured

The primary outcome is the main question the study is designed to answer.

1) Healthy Parenting Behaviors Measurement #1
Will participants report significantly healthier parenting behavior at program exit, as compared to responses at baseline?
Items measured include:
Parenting behavior measured with:
13 items depending on child age - 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 scores together and dividing by 13. 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
Measured: change from baseline in parenting behaviors (interactions with child) from enrollment to program exit (10 weeks).
2) Healthy Co-parenting Behaviors Measurement #1
Will participants report significantly healthier co-parenting behavior at program exit, as compared to responses at baseline?
Items measured include:
5 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.
maximum score: 5.0, minimum score: 1.0
Measured: change from baseline in co-parenting behaviors (interactions with co-parent) from enrollment to program exit (10 weeks).
3) Economic Stability Measurement #1
Will participants report significantly healthier economic stability at program exit, as compared to responses at baseline?
Items measured include:
1 items: yes or no questions for have checking/savings account (dichotomous)
1=yes, 0=no
Measured: change from baseline in economic stability from enrollment to program exit (10 weeks).
4) Economic Stability Measurement #2
Will participants report significantly healthier economic stability at program exit, as compared to responses at baseline?
Items measured include:
1 item: frequency of difficulty paying bills (categorical, 4-point scale)
Measured on the economic stability scale #1 as:
1 = never, 2 = once in a while, 3 = somewhat often, 4 = very often The lower the score, the better the outcome.
Measured: change from baseline in economic stability from enrollment to program exit (10 weeks).

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

1 Apr 202129 Aug 2025

First posted2 Apr 2025
Study start1 Apr 2021
Primary completion15 Jan 2025
Study completion29 Aug 2025

Resources

Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
Posted resultsParticipant flow, outcome measures and adverse events reported by the sponsor.
Other trials for FathersStudies of the same condition, open and under way.
What the trial phases meanHow a treatment moves from first tests in people to approval.

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design

Study type: Interventional
Phase: Phase N/A
Primary purpose: Other
Allocation: Not applicable
Intervention model: Single group
Masking: None (open label)
Enrolment: 996 participants (actual)

IDs, dates and publications

ClinicalTrials.gov ID: NCT06907719
Sponsor's protocol ID: #2021/03/41
Status last verified: Sep 2025
First submitted: 21 Mar 2025
Last updated: 1 Oct 2025
Results posted: Yes, on ClinicalTrials.gov
Data monitoring committee: No
FDA-regulated drug: No
FDA-regulated device: No
Individual data sharing: No: 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.

Want to know more?

The sponsor has not listed a contact. The official record may have more details.

Talk to your doctor first and take this page with you. Only the study team can confirm whether you can join.

Questions to ask the study team

What is the study trying to find out?
What would I need to do, and how often would I visit?
Could I receive a placebo instead of the treatment?
What are the possible risks and benefits for me?
Will it cost me anything? Are travel or time paid for?
Can I keep seeing my own doctor during the study?
What happens when the study ends?

See locations

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Effectiveness of GEMPO E-Education on Fathers' Self-Efficacy and Ability in Newborn Care
Fathers' Self-Efficacy and Ability in Newborn Care
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Determining the Effectiveness of Working Out Dads to Reduce Mental Health Difficulties in Fathers of Young Children
Mental Health Issue
Not yet recruiting
Mobile Prenatal Education for Expectant Fathers and Its Effects on Bonding, Stress, Breastfeeding and Marital Satisfaction
Breastfeeding Attitudes, Breast Feeding

All Fathers trials

Study at a glance

From the registry record, last updated by the sponsor on 1 Oct 2025. Recruitment status is as the sponsor reported it: confirm with the study team.

Official title: Strong Fathers, Stronger Families Program Evaluation
ClinicalTrials.gov ID: NCT06907719
Acronym / sponsor ID: #2021/03/41
Conditions: Fathers
Study type: Interventional
Recruitment status: Completed
Enrolment: 996 participants (actual)
Lead sponsor: Midwest Evaluation & ResearchUniversity, hospital or other
Collaborators: Seedco: Strong Fathers, Stronger Families
Study start: 1 Apr 2021 (actual)
Primary completion: 15 Jan 2025 (actual)
Study completion: 29 Aug 2025 (actual)
First posted: 2 Apr 2025 (actual)
Results: Posted 1 Oct 2025

Clinical summary

The research question as the sponsor registered it. This describes what the study plans to test, not what it found.

Detailed description

Study design

Primary purpose: Other
Allocation: Not applicable
Intervention model: Single group
Masking: None (open label)
Number of arms: 1

Arm	Type	Receives
Primary Services	Experimental	Other: Primary ServicesPrimary Services Participants receive 40 hours of the Blueprint and 24/7 Dad curricula over the course of ten weeks.

Who may qualify

Ages: 18 years and older
Sex: Male only
Healthy volunteers: Accepted
Age groups: Adult, Older adult

Key inclusion criteria (4 listed)

Adult (age 18 and older)
With children ages 0-24
Father/father figure
Reside in Memphis metropolitan area

Key exclusion criteria (4 listed)

Minor (under the age of 18)
Not a father/father figure
Children older than 24 years old
Reside outside of Memphis metropolitan area

Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.

Interventions

Intervention	Type	Arms
Primary ServicesParticipants receive 40 hours of the Blueprint and 24/7 Dad curricula over the course of ten weeks.	Other	Primary Services

Primary outcome

1) Healthy Parenting Behaviors Measurement #1
Time frame: change from baseline in parenting behaviors (interactions with child) from enrollment to program exit (10 weeks).
Will participants report significantly healthier parenting behavior at program exit, as compared to responses at baseline? Items measured include: Parenting behavior measured with: 13 items depending on child age - 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 scores together and dividing by 13. 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
2) Healthy Co-parenting Behaviors Measurement #1
Time frame: change from baseline in co-parenting behaviors (interactions with co-parent) from enrollment to program exit (10 weeks).
Will participants report significantly healthier co-parenting behavior at program exit, as compared to responses at baseline? Items measured include: 5 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. maximum score: 5.0, minimum score: 1.0
3) Economic Stability Measurement #1
Time frame: change from baseline in economic stability from enrollment to program exit (10 weeks).
Will participants report significantly healthier economic stability at program exit, as compared to responses at baseline? Items measured include: 1 items: yes or no questions for have checking/savings account (dichotomous) 1=yes, 0=no
4) Economic Stability Measurement #2
Time frame: change from baseline in economic stability from enrollment to program exit (10 weeks).
Will participants report significantly healthier economic stability at program exit, as compared to responses at baseline? Items measured include: 1 item: frequency of difficulty paying bills (categorical, 4-point scale) Measured on the economic stability scale #1 as: 1 = never, 2 = once in a while, 3 = somewhat often, 4 = very often The lower the score, the better the outcome.

Results and safety

Results posted to the registry on 1 Oct 2025, as reported by the sponsor. Figures are copied from the record, not re-analysed. Full results on ClinicalTrials.gov.

Participant flow

Group	Started	Completed
Primary Services	996	996

Primary outcome: 1) Healthy Parenting Behaviors Measurement #1

Time frame: change from baseline in parenting behaviors (interactions with child) from enrollment to program exit (10 weeks).. Mean (Standard Deviation). Unit: score on scale

Measure	Primary Services n = 342
mean at baseline	3.92 (.945)
mean at follow-up	3.97 (.883)

Primary outcome: 2) Healthy Co-parenting Behaviors Measurement #1

Time frame: change from baseline in co-parenting behaviors (interactions with co-parent) from enrollment to program exit (10 weeks).. Mean (Standard Deviation). Unit: score on scale

Measure	Primary Services n = 469
mean at baseline	3.61 (1.26)
mean at follow-up	3.70 (1.20)

Primary outcome: 3) Economic Stability Measurement #1

Time frame: change from baseline in economic stability from enrollment to program exit (10 weeks).. Count of participants. Unit: Participants

Measure	Primary Services n = 711
have checking account at baseline	98
have checking account at follow-up	380

Primary outcome: 4) Economic Stability Measurement #2

Time frame: change from baseline in economic stability from enrollment to program exit (10 weeks).. Mean (Standard Deviation). Unit: score on scale

Measure	Primary Services n = 718
mean at baseline	2.64 (1.005)
mean at follow-up	2.87 (.931)

Adverse events

Time frame: length of study involvement: 10 weeks. Other adverse events reported at 0% frequency or more

Group	Serious adverse events	Other adverse events	Deaths
Primary Services	0 of 996 (0%)	0 of 996 (0%)	0 of 996

Loading the posted results from ClinicalTrials.gov…

Research links

Official record on ClinicalTrials.govLast updated by the sponsor 1 Oct 2025.
Posted resultsParticipant flow, baseline, all outcome measures and adverse events.
Individual participant dataSharing planned: No. 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.

Related trials for Fathers

Recruiting
Online Feeding Education for Fathers of Children With Feeding Problems
Feeding Problems, Parent Training
Recruiting
Fathers and Babies (FAB) Research Study
Perinatal Mental Health, Fathers
Not yet recruiting
Effectiveness of GEMPO E-Education on Fathers' Self-Efficacy and Ability in Newborn Care
Fathers' Self-Efficacy and Ability in Newborn Care
Active, not recruiting
Determining the Effectiveness of Working Out Dads to Reduce Mental Health Difficulties in Fathers of Young Children
Mental Health Issue
Not yet recruiting
Mobile Prenatal Education for Expectant Fathers and Its Effects on Bonding, Stress, Breastfeeding and Marital Satisfaction
Breastfeeding Attitudes, Breast Feeding

Referral and contact

AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.

Matt D Shepherd, PhD principal investigator

Midwest Evaluation and Research

1 site in 1 country: see every site and its status.

Questions about this trial

What is this clinical trial studying?

A study testing Primary Services in people with Fathers, run by Midwest Evaluation & Research at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 1 Oct 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Yes. Results are posted in the registry (first posted 1 Oct 2025). A summary is in the For doctors view, and the full results are on ClinicalTrials.gov.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

1) Healthy Parenting Behaviors Measurement #1 (time frame: change from baseline in parenting behaviors (interactions with child) from enrollment to program exit (10 weeks).). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT06907719.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 1 Oct 2025.