- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03962764
Growing Responsible Fathers Descriptive Program Evaluation
Study Overview
Status
Conditions
Intervention / Treatment
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
Enrollment (Actual)
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Fathers or father figure
Exclusion Criteria:
-
Study Plan
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
Sponsor
Collaborators
Investigators
- Principal Investigator: Jeff Will, University of North Florida
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 (Estimated)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
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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