Evaluation of AVANCE Fathers in Action/Padres Activos Fatherhood Program (AVANCE)

November 15, 2017 updated by: Cynthia Osborne, University of Texas at Austin

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

Terminated

Conditions

Study Type

Interventional

Enrollment (Actual)

94

Phase

  • Not Applicable

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

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

Male

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

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: 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:
  • FA/PA program
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

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

Investigators

  • Principal Investigator: Cynthia Osborne, PhD, University of Texas at Austin

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)

August 1, 2016

Primary Completion (Actual)

September 1, 2017

Study Completion (Actual)

September 1, 2017

Study Registration Dates

First Submitted

July 28, 2016

First Submitted That Met QC Criteria

August 1, 2016

First Posted (Estimate)

August 4, 2016

Study Record Updates

Last Update Posted (Actual)

November 17, 2017

Last Update Submitted That Met QC Criteria

November 15, 2017

Last Verified

November 1, 2017

More Information

Terms related to this study

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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