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

1. september 2026 oppdatert 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

Studieoversikt

Status

Har ikke rekruttert ennå

Forhold

Intervensjon / Behandling

Studietype

Intervensjonell

Registrering (Antatt)

8

Fase

  • Ikke aktuelt

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Nei

Beskrivelse

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

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: N/A
  • Intervensjonsmodell: Enkeltgruppeoppdrag
  • Masking: Ingen (Open Label)

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Feasibility of STAR Intervention in Dyads
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. oktober 2026

Primær fullføring (Antatt)

1. mars 2031

Studiet fullført (Antatt)

1. mars 2031

Datoer for studieregistrering

Først innsendt

13. mai 2026

Først innsendt som oppfylte QC-kriteriene

13. mai 2026

Først lagt ut (Faktiske)

19. mai 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

4. september 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

1. september 2026

Sist bekreftet

1. september 2026

Mer informasjon

Begreper knyttet til denne studien

Andre studie-ID-numre

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

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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