Victim Impact Modules for Jail Inmates
21. april 2017 opdateret af: June Tangney, George Mason University
Phase 1-2 Study of Victim Impact Group Modules for Jail Inmates
The purpose of this study is to evaluate feasibility of modularized delivery of the Impact of Crime (IOC) group intervention with jail inmates, and obtain preliminary data on its effectiveness in reducing post-release recidivism, substance abuse, and HIV risk behavior.
Studieoversigt
Status
Trukket tilbage
Betingelser
Intervention / Behandling
Undersøgelsestype
Interventionel
Fase
- Ikke anvendelig
Kontakter og lokationer
Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.
Studiesteder
-
-
Virginia
-
Fairfax, Virginia, Forenede Stater, 22030
- Fairfax County Adult Detention Center
-
-
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
Ja
Køn, der er berettiget til at studere
Han
Beskrivelse
Inclusion Criteria:
- Must be 18 years or older
- Must be male
- Must be currently incarcerated jail inmate
- Must be sentenced
- Sentence must be short enough to serve out sentence at ADC
- Release date must follow projected final session of treatment
- Must speak, read, and write in English with sufficient proficiency to use workbook and participate in group sessions
- Must be assigned to the jail's "general population"
Exclusion Criteria:
- Actively psychotic
- Assigned "keep separate" from other group members
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: Dobbelt
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: Impact of Crime Modules
5 session/1 week modules of a restorative justice inspired victim impact group intervention
|
5 session/1 week modules of a restorative justice inspired victim impact group intervention
|
|
Andet: TAU
treatment as usual -- participants have access to all other jail programs and services
|
have access to other jail programs and services
|
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Recidivism - Self report of arrests and undetected crimes
Tidsramme: 3 months post-release up to 9 mos
|
3 months post-release up to 9 mos
|
|
Acceptability - number of participants who indicate the module was helpful and number who would recommend treatment to a friend
Tidsramme: 1 week post-treatment up to 2 weeks
|
1 week post-treatment up to 2 weeks
|
|
Number of inmates who complete the intervention
Tidsramme: 5 sessions over a period of 1 week
|
5 sessions over a period of 1 week
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Self reported Substance use and dependence -Texas Christian University measure
Tidsramme: 3 months post-release up to 9 mos
|
3 months post-release up to 9 mos
|
|
Self reported HIV risk behavior (sex and Intravenous Drug Use) Texas Christian University measure
Tidsramme: 3 months post-release up to 9 mos
|
3 months post-release up to 9 mos
|
|
Changes in self-reported Shame-proneness from baseline
Tidsramme: Changes from pre- to post-treatment up to 12 weeks
|
Changes from pre- to post-treatment up to 12 weeks
|
|
Changes in self-reported Shame-proneness from baseline
Tidsramme: Changes from pre-treatment to 3 mos post-release up to 9 mos
|
Changes from pre-treatment to 3 mos post-release up to 9 mos
|
|
Changes in self-reported Guilt-proneness from baseline
Tidsramme: Changes from pretreatment to 3 months post-release up to 9 mos
|
Changes from pretreatment to 3 months post-release up to 9 mos
|
|
Changes in self-reported Guilt-proneness from baseline
Tidsramme: Changes from pretreatment to post-treatment up to 12 weeks
|
Changes from pretreatment to post-treatment up to 12 weeks
|
|
Changes in self-reported empathy from baseline
Tidsramme: changes from pre- to post-treatment up to 12 weeks
|
changes from pre- to post-treatment up to 12 weeks
|
|
Changes in self-reported empathy from baseline
Tidsramme: changes from pre-treatment to 3 mos post-release up to 9 mos
|
changes from pre-treatment to 3 mos post-release up to 9 mos
|
|
Changes in self reported criminogenic thinking from baseline
Tidsramme: changes from pre-treatment to post-treatment up to 12 weeks
|
changes from pre-treatment to post-treatment up to 12 weeks
|
|
Changes in self reported criminogenic thinking from baseline
Tidsramme: changes from pre-treatment to 3 mos post-release up to 9 mos
|
changes from pre-treatment to 3 mos post-release up to 9 mos
|
Samarbejdspartnere og efterforskere
Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.
Sponsor
Samarbejdspartnere
Efterforskere
- Ledende efterforsker: June P Tangney, Ph.D., George Mason University
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 (Faktiske)
15. juli 2016
Primær færdiggørelse (Faktiske)
15. juli 2016
Studieafslutning (Faktiske)
15. juli 2016
Datoer for studieregistrering
Først indsendt
17. juni 2011
Først indsendt, der opfyldte QC-kriterier
23. juni 2011
Først opslået (Skøn)
27. juni 2011
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
25. april 2017
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
21. april 2017
Sidst verificeret
1. april 2017
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
Andre undersøgelses-id-numre
- R01DA014694-12 (U.S. NIH-bevilling/kontrakt)
- R01DA014694 (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 .