- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02855996
Evaluation of AVANCE Fathers in Action/Padres Activos Fatherhood Program (AVANCE)
The Child and Family Research Partnership (CFRP) will be conducting the "local" evaluation of AVANCE's Fathers in Action/Padres Activos (FA/PA) fatherhood program. AVANCE is a non-profit organization that has served low-income families and children since its founding in 1973. AVANCE sites have been providing fatherhood services for some time, but the programming offered has varied across sites and no rigorous evaluation of the programs has been completed. Through a federally-funded Responsible Fatherhood grant, AVANCE aims to create one fatherhood curriculum to be used across their sites: Fathers in Action/Padres Activos (FA/PA).
The purpose of the study is to advance the field of knowledge in the area of fatherhood programing by providing rigorous evidence on the impact of a comprehensive fatherhood program on enhancing a father's ability to be involved with and parent his child, in addition to providing more information on the selective characteristics of fathers who choose to participate in fatherhood programs. The study will seek to answer the following research questions: (1) What are the demographic and relationship characteristics of fathers who choose to participate in the Fathers in Action/Padres Actívos (FA/PA) program, and how do these characteristics compare to the fathers associated with mothers and children in other AVANCE programs?; (2) Does the FA/PA program positively impact parenting and co-parenting, father engagement and involvement, and healthy relationship?; (3) Are the program impacts similar for low-income fathers across regions (Houston v. the Rio Grande Valley), race/ethnicity (African American v. Hispanic), and coresidential status (nonresident v. resident)?; and (4) What are the factors that enhance or impede the successful implementation of the FA/PA program?
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Fathers (biological, adoptive, or social) over 18 years of age
- Able to travel to program location to attend classes
Exclusion Criteria:
- Under 18 years of age
- Female
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Intervention
Fathers will be randomly assigned to participate in the "Fathers in Action/Padres Activos (FA/PA)" intervention program to support fathers' healthy relationships with their children and support their co-parenting skills.
|
The program focuses on increasing the father's role in the child's education, nurturing and bonding with the child, loving and respecting the child's mother, coaching the child, and serving as a role model.
The program also includes employment coaching.
Other Names:
|
|
No Intervention: Control
Fathers waitlisted for participation in the "Fathers in Action/Padres Activos (FA/PA)" program.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of fathers reporting healthy father-child involvement and bond
Time Frame: Six months
|
Increase healthy father-child involvement and bond (connectedness) among residential and non-residential fathers of children 0-5 years.
Scale of items (never - often) aggregated to create a score on the outcome.
Will report number of treatment fathers whose score is higher than control group fathers at 6 months.
|
Six months
|
|
Number of fathers reporting healthy co-parenting relationship
Time Frame: Six months
|
Establish and maintain healthy co-parenting relationship among residential and non-residential fathers of children 0-5 years.
Scale of items (never - always) aggregated to create a score on the outcome.
Will report number of treatment fathers whose score is higher than control group fathers at 6 months.
|
Six months
|
|
Number of fathers reporting development of "self as father"
Time Frame: Six months
|
Strengthen the development of "self as father" among residential and non-residential fathers of children 0-5 years.
Several items (anger and stress management, financial stability, personal development) aggregated to create a score on the outcome.
Will report number of treatment fathers whose score is higher than control group fathers at 6 months.
|
Six months
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Cynthia Osborne, PhD, University of Texas at Austin
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 (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- AVANCE
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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