- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02860988
Responsible Fatherhood Opportunities for Reentry & Mobility (ReFORM)
Study Overview
Detailed Description
Individuals with a criminal justice background (either incarcerated or on community supervision) and substance use issues will have the opportunity to enroll in services provided by the Mountain Comprehensive Care Center to focus on enhancing fatherhood and family situations.
The primary research questions focus on gauging the intervention's effectiveness in improving healthy relationship and responsible fatherhood outcomes. The intervention has several components targeting parenting skills, job training, relationship education, and case management/reentry support. Primary research questions include:
- Compared to the counterfactual condition, what is the impact of the intervention on parenting and co-parenting skills/behaviors, as measured by parental role satisfaction and confidence in parenting skills six months after release from incarceration?
- Compared to the counterfactual condition, what is the impact of the intervention on the likelihood that the participant will be employed six months after release from incarceration?
- Compared to the counterfactual condition, what is the impact of the intervention on the likelihood that the participant will be in a relationship six months after release from incarceration?
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Kentucky
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Lexington, Kentucky, United States, 40508
- University of Kentucky
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Male inmates at specific eastern Kentucky jail sites who are at least 18 years of age and not previously screened for the study
- Participants for the local evaluation will be identified as eligible fathers who have been tried and convicted as an adult; within 3 to 9 months of release; are low-income; and may be an expectant father, a biological father, an adoptive father or a stepfather or who a person who is acknowledged as a father figure (e.g., grandfather) of a dependent child or young adult child up to 24 years of age, and interested in participation.
Exclusion Criteria:
- N/A
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: MCCC Treatment
Participants in this condition received newly-supported reentry services to enhance fatherhood and parenting for individuals with substance use issues.
These services focus on responsible parenting, economic stability and mobility, and healthy marriage and relationships.
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Participants in this condition received newly-supported reentry services to enhance fatherhood and parenting for individuals with substance use issues.
These services focus on responsible parenting, economic stability and mobility, and healthy marriage and relationships.
|
|
No Intervention: MCCC Comparison
Participants in this condition did not receive reentry services related to responsible parenting, economic stability and mobility, or healthy marriage and relationships.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Parental Role Satisfaction
Time Frame: 6-month follow-up
|
A scale calculated by summing three times measuring happiness, closeness, and comforting interactions with the child.
Total score range is 3-12, with higher scores indicating greater satisfaction.
|
6-month follow-up
|
|
Number of Participants Employed
Time Frame: 6-month follow-up
|
The outcome is a dichotomous indicator of whether the participant currently has a job.
|
6-month follow-up
|
|
Number of Participants in a Relationship
Time Frame: 6-month follow-up
|
The outcome measure is a dichotomous indicator of whether the participant is currently in a relationship.
|
6-month follow-up
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of Participants With Recent In-person Contact With Child(Ren)
Time Frame: 6-month follow-up
|
The measure is a dichotomous indicator of whether the participant has seen their child in person during the past month.
|
6-month follow-up
|
|
Number of Participants With Recent Other Contact With Child(Ren)
Time Frame: 6-month follow-up
|
The measure is a dichotomous indicator of whether the participant has spoken with their child on the phone or sent their child letters within the past month.
|
6-month follow-up
|
|
Number of Participants That Participated in an Education or Job Training Program in the Past 30 Days
Time Frame: 6-month follow-up
|
The measure is a dichotomous indicator of whether the participant has participated in education or job training programs within the past month.
|
6-month follow-up
|
|
Partner Conflict Resolution
Time Frame: 6-month follow-up
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The measure is a Likert-type (very/somewhat/not at all satisfied) response to whether the participant is satisfied with the way that they and their partner/spouse handle conflict.
Total scores range 1-3, with higher scores indicating a greater level of satisfaction.
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6-month follow-up
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Mental Health Distress
Time Frame: 6-month follow-up
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The outcome measure is a scale calculated from six items measuring symptoms of anxiety and depression experienced in the past month.
Total scores range from 6-30,w with higher scores indicating more frequent experience with symptoms (i.e., greater distress).
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6-month follow-up
|
Collaborators and Investigators
Collaborators
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
Other Study ID Numbers
- 90FO0007-01-00
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
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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