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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01372033
Other study ID # R01DA017729
Secondary ID R01DA017729
Status Completed
Phase Phase 3
First received June 10, 2011
Last updated June 10, 2011
Start date June 2007
Est. completion date December 2010

Study information

Verified date June 2009
Source George Mason University
Contact n/a
Is FDA regulated No
Health authority United States: Federal Government
Study type Interventional

Clinical Trial Summary

The specific aims of this project are:

1. To conduct a randomized block experiment to test the effectiveness of different models of the seamless supervision/treatment system and traditional criminal justice supervision on reducing recidivism and drug use, and improving social adjustment among offenders;

2. To understand the differential impacts based on offender risk factors (e.g., propensity to engage in further criminal behavior) on criminal justice outcomes and to determine whether differences found between seamless and traditional system participants are moderated by offender risk level;

3. To understand differential treatment and social adjustment outcomes (e.g., treatment progress, employment status) of different types of offenders participating in various treatment services; and

4. To examine levels of systems and service integration between the supervision and treatment systems pre- and post-intervention and to measure the impact of integration on outcomes over time.


Recruitment information / eligibility

Status Completed
Enrollment 251
Est. completion date December 2010
Est. primary completion date December 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria:

- Substance abusers

- men and women

- treatment

Exclusion Criteria:

- Parolees

- Low threshold substance abuse

- violent offenders

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research


Intervention

Behavioral:
Cognitive Behavioral Therapy
18 sessions of CBT, twice weekly
Cognitive Behavioral Therapy
18 sessions with goals groups drug testing

Locations

Country Name City State
United States Maryland Dvision of Parole and Probation Baltimore Maryland

Sponsors (2)

Lead Sponsor Collaborator
George Mason University National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Arrest 12 months Yes
Secondary Treatment Completion 12 months No
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