Responsible Fatherhood Opportunities for Reentry & Mobility (ReFORM)
29 de abril de 2021 actualizado por: Mountain Comprehensive Care Center
The purpose of this study is to determine differences among incarcerated or recently incarcerated fathers who receive targeted services and those who do not.
Descripción general del estudio
Descripción detallada
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?
Tipo de estudio
Intervencionista
Inscripción (Actual)
401
Fase
- No aplica
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Ubicaciones de estudio
-
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Kentucky
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Lexington, Kentucky, Estados Unidos, 40508
- University of Kentucky
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Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
18 años y mayores (Adulto, Adulto Mayor)
Acepta Voluntarios Saludables
No
Géneros elegibles para el estudio
Masculino
Descripción
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
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: No aleatorizado
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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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.
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Sin intervención: MCCC Comparison
Participants in this condition did not receive reentry services related to responsible parenting, economic stability and mobility, or healthy marriage and relationships.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Parental Role Satisfaction
Periodo de tiempo: 6-month follow-up
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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.
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6-month follow-up
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Number of Participants Employed
Periodo de tiempo: 6-month follow-up
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The outcome is a dichotomous indicator of whether the participant currently has a job.
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6-month follow-up
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Number of Participants in a Relationship
Periodo de tiempo: 6-month follow-up
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The outcome measure is a dichotomous indicator of whether the participant is currently in a relationship.
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6-month follow-up
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Number of Participants With Recent In-person Contact With Child(Ren)
Periodo de tiempo: 6-month follow-up
|
The measure is a dichotomous indicator of whether the participant has seen their child in person during the past month.
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6-month follow-up
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Number of Participants With Recent Other Contact With Child(Ren)
Periodo de tiempo: 6-month follow-up
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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.
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6-month follow-up
|
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Number of Participants That Participated in an Education or Job Training Program in the Past 30 Days
Periodo de tiempo: 6-month follow-up
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The measure is a dichotomous indicator of whether the participant has participated in education or job training programs within the past month.
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6-month follow-up
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Partner Conflict Resolution
Periodo de tiempo: 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
Periodo de tiempo: 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
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Colaboradores
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Actual)
1 de julio de 2016
Finalización primaria (Actual)
31 de mayo de 2020
Finalización del estudio (Actual)
31 de mayo de 2020
Fechas de registro del estudio
Enviado por primera vez
2 de agosto de 2016
Primero enviado que cumplió con los criterios de control de calidad
4 de agosto de 2016
Publicado por primera vez (Estimar)
10 de agosto de 2016
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
30 de abril de 2021
Última actualización enviada que cumplió con los criterios de control de calidad
29 de abril de 2021
Última verificación
1 de abril de 2021
Más información
Términos relacionados con este estudio
Palabras clave
Otros números de identificación del estudio
- 90FO0007-01-00
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
NO
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .