Medication-Assisted Treatment Implementation in Community Correctional Environments (MATICCE)

NCT01344122 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2014-10-30

No results posted yet for this study

Summary

The goal of this study is to see whether or not a strategic planning process is able to introduce and sustain improvements in the working relationship between probation/parole departments and community-based addiction treatment agencies that provide medication assisted therapy (MAT) for individuals with opioid or alcohol dependence. In addition, this study seeks to improve probation/parole agency personnel's knowledge and perceptions about MAT, and increase the number of appropriate referrals to community treatment agencies that provide MAT. There are three phases to this study. Phase 1 includes a pilot study to determine the quality and availability of client level records and the collection of baseline data (the pilot study protocol was previously submitted to TMH IRB). Phase 2 will consist of a Knowledge, Perceptions and Information (KPI) intervention during which probation/parole agencies will undergo training to increase knowledge about the effectiveness of MAT, and complete a post training assessment to evaluate the effectiveness of the KPI intervention. During Phase 3, probation/parole agencies will be randomly assigned to a 12-month Organizational Linkage Intervention (OLI) condition or to control (no further intervention). Agencies assigned to the OLI will establish a Pharmacotherapy Exchange Council (PEC) that consists of staff from both the probation/parole and community treatment agencies. The PEC will undergo a strategic planning process to increase the availability of MAT for opiate and/or alcohol dependent individuals who are on probation/parole.

Conditions

  • Opioid-Related Disorders
  • Alcohol-Related Disorders

Interventions

OTHER

KPI training only

See comparison arm description.

OTHER

KPI plus OLI

See experimental arm description.

Sponsors & Collaborators

  • Arizona State University

    collaborator OTHER
  • Friends Research Institute, Inc.

    collaborator OTHER
  • National Development and Research Institutes, Inc.

    collaborator OTHER
  • National Institute on Drug Abuse (NIDA)

    collaborator NIH
  • Temple University

    collaborator OTHER
  • Texas Christian University

    collaborator OTHER
  • University of California, Los Angeles

    collaborator OTHER
  • University of Connecticut

    collaborator OTHER
  • University of Delaware

    collaborator OTHER
  • University of Kentucky

    collaborator OTHER
  • University of Puerto Rico

    collaborator OTHER
  • Rhode Island Hospital

    lead OTHER

Principal Investigators

  • Peter D Friedmann, MD, MPH · Rhode Island Hospital

Study Design

Allocation
RANDOMIZED
Masking
NONE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2010-10-31
Primary Completion
2013-09-30
Completion
2013-09-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01344122 on ClinicalTrials.gov