Support Towards Addiction Recovery for Individuals With Criminal Legal System Involvement: The STAR Project
1 de septiembre de 2026 actualizado por: Martha Tillson
The goal of this clinical trial is to determine whether a new, paired coaching intervention improves outcomes for individuals with criminal legal system involvement recovering from substance use disorder, as well as the loved ones of those individuals. The initial phase (Year 1) includes a small preliminary pilot examining the feasibility of the intervention.
During the full clinical trial (Years 2-5), this study aims to answer whether this approach...
- ...improves the recovering person's recovery capital?
- ...improves well-being, as well as resource knowledge and awareness, for the loved one?
- ...improves social support and connection among both individuals?
Participants will:
- Meet regularly one-on-one with their individual coaches (a Recovery Coach for the recovering person; a Loved One Coach for the loved one) during the 6 week intervention period
- Meet regularly as a group of four (both coaches and both participants) during this same period
- Complete follow-up interviews with research staff at 6- and 12-weeks after beginning the study
Descripción general del estudio
Estado
Aún no reclutando
Condiciones
Intervención / Tratamiento
Tipo de estudio
Intervencionista
Inscripción (Estimado)
8
Fase
- No aplica
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
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
No
Descripción
Inclusion Criteria:
- Recovering Persons:
- At least 18 years old
- Must have been involved with the criminal legal system (arrested, incarcerated, or on community supervision like parole or probation) within the past 12 months
- Substance use disorder within the past 12 months
- Interested in working with a recovery coach to support your recovery (defined as engaging in any changes to improve your health and wellness)
- Can identify at least one person who is supportive of their recovery.
- Loved Ones:
- At least 18 years old
- Interested in receiving additional supports and/or information about their loved one's substance use and criminal legal system involvement
- Anticipate being available for weekly participation in intervention activities
- Willing to support their loved one's recovery
Exclusion Criteria:
- Loved ones:
- Already have a professional relationship with the recovering person (e.g., as a counselor, sponsor, or peer recovery support specialist)
- Meet substance use disorder criteria for any past 30-day drug or alcohol use
- Have a history of domestic violence or protective orders.
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: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: STAR Intervention
|
The STAR intervention is a dyadic coaching model designed to support individuals with substance use disorder and criminal legal system involvement alongside their identified loved ones.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Feasibility of STAR Intervention in Dyads
Periodo de tiempo: Immediately following intervention sessions during 6-week feasibility pilot.
|
a. Feasibility will be assessed using the STAR Project Focus Group Survey questions administered to dyad participants following intervention sessions.
A higher score indicates greater perceived feasibility.
|
Immediately following intervention sessions during 6-week feasibility pilot.
|
|
Acceptability of STAR Intervention in Dyads
Periodo de tiempo: Immediately following intervention sessions during 6-week feasibility pilot.
|
a. Acceptability will be assessed using the Focus Group Survey questions administered to dyad participants following intervention sessions.
A higher score indicates greater perceived acceptability.
|
Immediately following intervention sessions during 6-week feasibility pilot.
|
|
Recovery capital
Periodo de tiempo: Assessed at enrollment and 6- and 12-weeks post-enrollment
|
a.
For recovering persons: The internal and external resources that impact an individual's capacity to initiate and sustain recovery, including physical, cultural, human, and social resources.
Assessed using the Multidimensional Inventory of Recovery Capital (MIRC) a 28-item questionnaire.
Higher scores indicate greater recovery capital.
|
Assessed at enrollment and 6- and 12-weeks post-enrollment
|
|
Psychological well-being
Periodo de tiempo: Assessed at enrollment and 6- and 12-weeks post-enrollment
|
a.
For loved ones: Positive affect, life satisfaction, and an overall sense of purpose and meaning.
Assessed using the Neuro-QOL Positive Affect and Well-Being Scale, a 23-item questionnaire, Higher scores indicate greater psychological well-being.
|
Assessed at enrollment and 6- and 12-weeks post-enrollment
|
|
SUD and CLS knowledge and resource awareness
Periodo de tiempo: Assessed at enrollment and 6- and 12-weeks post-enrollment
|
a.
For loved ones: Knowledge regarding Substance Use Disorder (SUD) including recovery, treatment, harm reduction, and Criminal Legal System (CLS) involvement as well as awareness of local recovery and resources.
Assessed using study developed knowledge assessment questions and count of local resources known.
Higher scores indicate greater knowledge and resource awareness.
|
Assessed at enrollment and 6- and 12-weeks post-enrollment
|
|
Support functions
Periodo de tiempo: Assessed at enrollment and 6- and 12-weeks post-enrollment
|
a.
For loved ones and recovering persons: Number and types of support functions provided by social network members.
Assessed using egocentric social network inventory questionnaire evaluating functional support provided by network members.
Higher scores indicate greater perceived social support.
|
Assessed at enrollment and 6- and 12-weeks post-enrollment
|
|
Social connection
Periodo de tiempo: Assessed at enrollment and 6- and 12-weeks post-enrollment
|
a.
For loved ones and recovering persons: Level of trust, emotional closeness, and frequency of contact with social network members.
Assessed using egocentric social network inventory questionnaire.
Higher scores indicate stronger social connection and network engagement.
|
Assessed at enrollment and 6- and 12-weeks post-enrollment
|
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 (Estimado)
1 de octubre de 2026
Finalización primaria (Estimado)
1 de marzo de 2031
Finalización del estudio (Estimado)
1 de marzo de 2031
Fechas de registro del estudio
Enviado por primera vez
13 de mayo de 2026
Primero enviado que cumplió con los criterios de control de calidad
13 de mayo de 2026
Publicado por primera vez (Actual)
19 de mayo de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
4 de septiembre de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
1 de septiembre de 2026
Última verificación
1 de septiembre de 2026
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 111148
- R61DA064790 (Subvención/contrato del NIH de EE. UU.)
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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. .