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Support Towards Addiction Recovery for Individuals With Criminal Legal System Involvement: The STAR Project

1 september 2026 uppdaterad av: 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

Studieöversikt

Status

Har inte rekryterat ännu

Betingelser

Intervention / Behandling

Studietyp

Interventionell

Inskrivning (Beräknad)

8

Fas

  • Inte tillämpbar

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

  • Vuxen
  • Äldre vuxen

Tar emot friska volontärer

Nej

Beskrivning

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.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: N/A
  • Interventionsmodell: Enskild gruppuppgift
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: 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.

Vad mäter studien?

Primära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Feasibility of STAR Intervention in Dyads
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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
Tidsram: 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

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Beräknad)

1 oktober 2026

Primärt slutförande (Beräknad)

1 mars 2031

Avslutad studie (Beräknad)

1 mars 2031

Studieregistreringsdatum

Först inskickad

13 maj 2026

Först inskickad som uppfyllde QC-kriterierna

13 maj 2026

Första postat (Faktisk)

19 maj 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

4 september 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

1 september 2026

Senast verifierad

1 september 2026

Mer information

Termer relaterade till denna studie

Andra studie-ID-nummer

  • 111148
  • R61DA064790 (U.S.S. NIH-anslag/kontrakt)

Läkemedels- och apparatinformation, studiedokument

Studerar en amerikansk FDA-reglerad läkemedelsprodukt

Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

Denna information hämtades direkt från webbplatsen clinicaltrials.gov utan några ändringar. Om du har några önskemål om att ändra, ta bort eller uppdatera dina studieuppgifter, vänligen kontakta register@clinicaltrials.gov. Så snart en ändring har implementerats på clinicaltrials.gov, kommer denna att uppdateras automatiskt även på vår webbplats .

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