Denne side blev automatisk oversat, og nøjagtigheden af ​​oversættelsen er ikke garanteret. Der henvises til engelsk version for en kildetekst.

Transitional Case Management Study

16. november 2016 opdateret af: University of California, Los Angeles
To address the issues involved in treatment participation by substance-abusing parolees, the CJ-DATS Transitional Case Management (TCM) study proposes to test a parole re-entry model that consists of (1) completion by the inmate of a strengths and goals assessment as part of discharge planning, (2) a telephone case conference call that includes the inmate and significant members of the inmate's aftercare plan (including the parole officer), and (3) strengths case management (for 12 weeks) in the community to promote treatment participation and support the client's access to needed services.

Studieoversigt

Status

Afsluttet

Detaljeret beskrivelse

To address the issues involved in treatment participation by substance-abusing parolees, the CJ-DATS Transitional Case Management (TCM) study proposes to test a parole re-entry model that consists of (1) completion by the inmate of a strengths and goals assessment as part of discharge planning, (2) a telephone case conference call that includes the inmate and significant members of the inmate's aftercare plan (including the parole officer), and (3) strengths case management (for 12 weeks) in the community to promote treatment participation and support the client's access to needed services.

More specifically, the multi-site study will evaluate the effects of a strengths case-management intervention on community-based treatment/service admission, retention, and utilization among inmates released from supervised treatment programs. If the intervention is successful, its wider adoption would increase the likelihood that inmates enter and remain in community services.

The specific aims of this multi-site study are to:

  1. Increase the likelihood that offenders leaving prison (or other supervised setting) with a referral to community aftercare program services enroll in treatment.
  2. Increase the amount of time that such offenders participate in community treatment.
  3. Assist clients to get the services that they need during the first 12 weeks of return to the community.
  4. As a result of the above, reduce relapse and reoffending during and following treatment.
  5. Achieve the above results at a favorable cost-effectiveness ratio.
  6. Encourage closer collaboration between the treatment and criminal justice systems.

Study participants (200 at each site, 25% of will be women) will be recruited in prison (or other confined setting) from inmates who have a referral to community treatment. After informed consent and a baseline interview, they will be randomly assigned to one of two conditions: (1) the Transitional Case Management condition, and (2) the Standard Referral condition (i.e., usual transition/re-entry procedures used by the facility, including a referral to community treatment).

Individual-level outcomes will include (1) treatment admission and participation (based on data collected from programs), (2) drug use, criminal activity, and psychosocial functioning (based on telephone interviews conducted 3 months after the end of the intervention) and (3) recidivism (based on records collected 12 months after the end of the intervention). The study will also assess the impact of the intervention on organizational and system factors (based on information from the case manager, treatment staff, and criminal justice staff) and the cost effectiveness of the intervention.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

812

Fase

  • Fase 3

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

    • California
      • Los Angeles, California, Forenede Stater, 90025
        • University of California, Los Angeles
    • Connecticut
      • Hartford, Connecticut, Forenede Stater, 06134
        • Connecticut Department of Mental Health and Addiction Services
    • Kentucky
      • Lexington, Kentucky, Forenede Stater, 40506
        • University of Kentucky
    • New York
      • New York, New York, Forenede Stater, 10048
        • National Development and Research Institutes, Inc. (NDRI)

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år og ældre (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

Inclusion Criteria:

  • Age 18 years or older
  • Participate in a treatment program within a correctional institution (prison, work release, community correctional facility)
  • Have a referral to a community-based substance abuse treatment program (as arranged by correctional staff or treatment staff)
  • Within about 3 months until release
  • Being released to the metropolitan area where case manager activities are being conducted

Exclusion Criteria:

  • Referral to formal case management services in the community (e.g., for offenders with co-occurring disorders)
  • Inability to provide informed consent (as determined by a set of questions about the consent process)
  • Registered sex offender (as determined by the institution)
  • Parole requirements that would prevent participation in the study (e.g., INS hold for deportation)

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Ingen (Åben etiket)

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Tidsramme
Treatment admission by three months following parole
Tidsramme: Three months
Three months
Treatment retention by three months following parole
Tidsramme: Three months
Three months
Drug use at nine months following parole
Tidsramme: Nine months
Nine months
Recidivism at nine months following parole
Tidsramme: Nine months
Nine months

Sekundære resultatmål

Resultatmål
Tidsramme
Education and employment at nine months following parole
Tidsramme: Nine months
Nine months
HIV risk behaviors at nine months following parole
Tidsramme: Nine months
Nine months

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Efterforskere

  • Ledende efterforsker: Michael L Prendergast, Ph.D., University of California, Los Angeles
  • Studieleder: Jerome Cartier, M.S., University of California, Los Angeles

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart

1. november 2004

Primær færdiggørelse (Faktiske)

1. april 2006

Studieafslutning (Faktiske)

1. maj 2008

Datoer for studieregistrering

Først indsendt

8. december 2005

Først indsendt, der opfyldte QC-kriterier

8. december 2005

Først opslået (Skøn)

12. december 2005

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Skøn)

18. november 2016

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

16. november 2016

Sidst verificeret

1. november 2016

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • U01DA016211 (U.S. NIH-bevilling/kontrakt)

Disse oplysninger blev hentet direkte fra webstedet clinicaltrials.gov uden ændringer. Hvis du har nogen anmodninger om at ændre, fjerne eller opdatere dine undersøgelsesoplysninger, bedes du kontakte register@clinicaltrials.gov. Så snart en ændring er implementeret på clinicaltrials.gov, vil denne også blive opdateret automatisk på vores hjemmeside .

Abonner