- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01378936
Jail-Based Impact of Crime Intervention (IOC)
May 3, 2013 updated by: June Tangney, George Mason University
Phase 2 RCT of Jail-Based Impact of Crime Intervention to Reduce Recidivism, Substance Abuse and HIV Risk Behavior
The purpose of this study is to evaluate whether the Impact of Crime (IOC) group intervention with jail inmates reduces post-release recidivism, substance abuse, and HIV risk behavior.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Detailed Description
This project imports social-personality theory and research on moral emotions and cognitions to the applied problems of crime, substance abuse, and HIV risk behavior.
The primary aim of this study, a Phase 2 Randomized Clinical Trial (RCT) of the restorative justice-inspired Impact of Crime (IOC) group intervention, is to examine the efficacy of treatment and to determine if changes in moral emotions and cognitions serve as mechanisms of action, explaining the impact of treatment involvement on reductions in post-release recidivism, substance abuse, and HIV risk behavior.
Study Type
Interventional
Enrollment (Anticipated)
200
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Virginia
-
Fairfax, Virginia, United States, 22030
- Fairfax County Adult Detention Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Description
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
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: MI plus IOC group intervention
|
45 minute Motivational Interview plus 16 session IOC intervention
Other Names:
|
|
Experimental: Motivational Interview only
|
45 minute Motivational Interview session
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Recidivism - Self report of arrests and undetected crimes
Time Frame: 3 months post-release
|
3 months post-release
|
|
Recidivism - Self report of arrests and undetected crimes
Time Frame: 1 yr post-release
|
1 yr post-release
|
|
Recidivism - Self report of arrests and undetected crimes
Time Frame: 3 yr post-release
|
3 yr post-release
|
|
Recidivism - Self report of arrests and undetected crimes
Time Frame: 5 yr post-release
|
5 yr post-release
|
|
Recidivism -- official FBI records of arrests
Time Frame: 1 yr post-release
|
1 yr post-release
|
|
Recidivism -- official FBI records of arrests
Time Frame: 3 yr post-release
|
3 yr post-release
|
|
Recidivism -- official FBI records of arrests
Time Frame: 5 yr post-release
|
5 yr post-release
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Changes in self-reported shame-proneness from baseline
Time Frame: changes from baseline to post tx and 3 mo, 1 yr, 3yr and 5 yr post-release
|
changes from baseline to post tx and 3 mo, 1 yr, 3yr and 5 yr post-release
|
|
Changes in self-reported guilt proneness from baseline
Time Frame: changes from baseline to post tx, and 3 mo, 1 yr, 3 yr, 5 yr post-release
|
changes from baseline to post tx, and 3 mo, 1 yr, 3 yr, 5 yr post-release
|
|
Changes from self-reported empathy from baseline
Time Frame: changes from baseline to post tx, 3 mo, 1 yr, 3 yr, 5 yr post-release
|
changes from baseline to post tx, 3 mo, 1 yr, 3 yr, 5 yr post-release
|
|
Changes from self-reported criminogenic thinking at baseline
Time Frame: changes from baseline to post tx, and 3 mo, 1 yr, 3 yr, 5 yr post-release
|
changes from baseline to post tx, and 3 mo, 1 yr, 3 yr, 5 yr post-release
|
|
Changes in self-reported substance use and dependence from 1 yr pre-incarceration
Time Frame: changes from pre-incarceration to 3 mo, 1 yr, 3 yr, 5 yr post-release
|
changes from pre-incarceration to 3 mo, 1 yr, 3 yr, 5 yr post-release
|
|
Changes in self-reported HIV risk behavior (sex and IDU) from 1 year pre-incarceration
Time Frame: changes from pre-incarceration to 3 mo, 1 yr, 3 yr, 5 yr post-release
|
changes from pre-incarceration to 3 mo, 1 yr, 3 yr, 5 yr post-release
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: June P Tangney, Ph.D., George Mason University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
August 1, 2009
Primary Completion (Anticipated)
December 1, 2013
Study Completion (Anticipated)
June 1, 2016
Study Registration Dates
First Submitted
June 17, 2011
First Submitted That Met QC Criteria
June 22, 2011
First Posted (Estimate)
June 23, 2011
Study Record Updates
Last Update Posted (Estimate)
May 7, 2013
Last Update Submitted That Met QC Criteria
May 3, 2013
Last Verified
May 1, 2013
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- R01DA014694-11 (U.S. NIH Grant/Contract)
- R01DA014694 (U.S. NIH Grant/Contract)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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