- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02056457
An Evaluation of Selected Responsible Fatherhood and Healthy Marriage Programs: Parents and Children Together (PACT)
Parents and Children Together
Study Overview
Status
Conditions
Detailed Description
Since 2006, Congress has provided funding for grants to provide healthy marriage and responsible fatherhood services to help interested couples and fathers enhance or improve adult and parent-child relationships and meet other objectives. The Administration for Children and Families (ACF), within the Department of Health and Human Services (HHS), oversees these grants and provides supports to assist grantees to meet their goals and objectives. To learn about the implementation and effects of these programs, ACF awarded a contract in 2011 to Mathematica Policy Research, Inc. to conduct the Parents and Children Together (PACT) evaluation. The evaluation includes separate impact and process studies for responsible fatherhood and healthy marriage programs.
Individuals who are eligible for the programs and agree to be in the study are randomly assigned to either a program group or a control group. Program group members are offered program services; control group members are not offered those services but are able to receive other services available in the community. The impact studies will examine whether the programs improve outcomes for fathers, mothers, families, and children in the program group compared to outcomes of those in the control group. Members of both program and control groups are surveyed twice: before they are randomly assigned and 12 months later. At the 12-month follow-up, both groups will be asked to complete a telephone survey. The survey will cover a range of questions related to adult relationships and interactions, parent-child interactions and economic stability. Corresponding process studies will examine multiple aspects of the implementation and operation of the programs. Information for the process studies will be obtained through: interviews with program and partner organization managers and staff; observations of program operations; from focus groups with program participants and non-participants; and from data from each grantee's management information system.
Study Type
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Florida
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Sarasota, Florida, United States
- Jewish Family and Children's Services
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Minnesota
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Minneapolis, Minnesota, United States
- Goodwill/Easter Seals Minnesota
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Minneapolis, Minnesota, United States
- Urban Ventures
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Missouri
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Kansas City, Missouri, United States
- Connections to Success
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Saint Louis, Missouri, United States
- Fathers' Support Center
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New York
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Bronx, New York, United States
- University Behavioral Associates
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Texas
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El Paso, Texas, United States
- El Paso Center for Children
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
To be eligible for the PACT HM Evaluation, the applicant must be part of a couple (as defined by the couple) in which both couple members are applying to the program and that:
- Both members of the couple are eligible for the program
- Both members of the couple are 18 years of age or older
- One member of the couple is female and the other male
- At least one member of the couple is an expectant parent or a parent of a biological or adoptive child who is living with him or her (That is the children do not need to be children in common and they need to be living with only one parent)
To be eligible for the PACT RF evaluation, the individual must:
- Be male
- Be 18 years or older
- Have a living biological or adopted child or is expecting a child
Exclusion Criteria:
- Does not meet the inclusion criteria
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Single Group Assignment
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Experimental: Control
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RF grantees funded by the most recent re-authorization of the program must offer services in each of three categories: (1) healthy marriage; (2) responsible parenting; and (3) economic stability.
HM grantees must provide one or more of eight allowable activities, which include marriage and relationship skills programs, mentoring, divorce reduction programs, and education in high schools on the value of marriage, relationships skills, and budgeting.
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Experimental: Responsible fatherhood or healthy marriage
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RF grantees funded by the most recent re-authorization of the program must offer services in each of three categories: (1) healthy marriage; (2) responsible parenting; and (3) economic stability.
HM grantees must provide one or more of eight allowable activities, which include marriage and relationship skills programs, mentoring, divorce reduction programs, and education in high schools on the value of marriage, relationships skills, and budgeting.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
In-person contact with child(ren) in past month
Time Frame: 12 months
|
12 months
|
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Earnings in past year
Time Frame: 12 months
|
12 months
|
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Co-parenting teamwork
Time Frame: 12 months
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Agreement with whether father and mother work well together as parents
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12 months
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Collaborators and Investigators
Collaborators
Investigators
- Study Director: Sheena McConnell, Ph.D., Mathematica Policy Research
- Study Director: Robin Dion, M.A., Mathematica Policy Research
Study record dates
Study Major Dates
Study Start
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
- MPR06997
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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