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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01104805
Other study ID # NYSPI #6051
Secondary ID U10DA013035NIDA-
Status Completed
Phase N/A
First received April 14, 2010
Last updated July 6, 2017
Start date April 2010
Est. completion date September 2012

Study information

Verified date July 2017
Source New York State Psychiatric Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The main objective of this study is to evaluate the effectiveness of including an interactive, web-based version of the Community Reinforcement Approach (CRA), called the Therapeutic Education System (TES), as part of community-based, outpatient substance abuse treatment.


Description:

The principal objective of the planned trial is to evaluate the effectiveness of including an interactive, web-based version of the Community Reinforcement Approach (CRA), called the Therapeutic Education System (TES), as part of community-based, outpatient substance abuse treatment. CRA is a cognitive-behavioral intervention which seeks to give patients skills to achieve and maintain abstinence and improve social functioning and is often paired with contingency management, where patients earn rewards contingent upon drug negative urines. CRA is an intensive treatment, generally delivered in individual sessions 2 to 3 times per week. Thus, it is expensive and time-consuming to deliver, to train clinical staff, and to provide supervision to maintain clinical staff skill. However, because CRA is oriented toward knowledge and skills, it lends itself to being delivered by computer, using computer-interactive learning technologies.

Individuals accepted into community-based outpatient treatment for substance use disorders (excluding those receiving opioid pharmacotherapy for opioid dependence) will be eligible to participate. This is a multi-site, controlled trial, using NIDA's Clinical Trials Network platform, at approximately 10 Community Treatment Programs, in which participants (N = approximately 500) will be randomized to receive 12 weeks of either: (1) Treatment-as-Usual (TAU), reflecting standard treatment at the collaborating treatment programs in which participants are enrolled, or (2) a modification of TAU which includes access to the TES. It is hypothesized that access to TES will improve substance use outcome and retention in outpatient treatment.

Computer interactive interventions like TES have the potential to deliver science-based psychosocial treatments with high fidelity and cost-effectiveness while conserving clinician time to focus on monitoring and addressing patients' needs. If found to be effective, TES could substantially advance the substance abuse treatment system by improving quality of care delivered, increasing availability of treatment slots by extending and leveraging the efforts of clinical staff, and projecting treatment to rural and other underserved areas.


Recruitment information / eligibility

Status Completed
Enrollment 507
Est. completion date September 2012
Est. primary completion date June 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Male and female patients, 18 years or older, accepted for outpatient, substance abuse treatment at a participating study site.

- Self-report any substance use problem (including alcohol, as long as they also report other drug use in addition to alcohol).

- Self-report recent drug use.

- Within 30 days of initiating treatment at a collaborating study site.

- Self-report a planned substance abuse treatment episode of at least 3 months.

Exclusion Criteria:

- Receiving opioid replacement medication.

- Plan to move out of the area within the next 3 months.

- Insufficient ability to provide informed consent.

- Insufficient ability to use English to participate meaningfully in the consent process, the interventions or research assessments.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Therapeutic Education System (TES)
Participants will received modified treatment-as-usual plus the computerized psychosocial intervention (Therapeutic Education System), including contingency management. Participants will be asked to use the self-directed TES intervention twice weekly and will be asked to complete 2 modules during each session (for a total of 4 modules per week) during the 12-week intervention. Participants will receive incentives contingent primarily upon abstinence from drugs of abuse and, secondarily, upon completion of TES modules.
Treatment-as-Usual (TAU)
Participants in this condition will receive TAU, consisting of standard treatment offered at each collaborating CTP and will reflect the model of treatment typically provided to most individuals in outpatient, community-based substance abuse treatment settings in the U.S. These sessions will consist of a combination of group and individual counseling.

Locations

Country Name City State
United States HARBEL Prevention and Recovery Center Baltimore Maryland
United States Homeward Bound Dallas Texas
United States MCCA: Midwestern CT Council on Alcoholism Danbury Connecticut
United States Willamette Family, Inc. Eugene Oregon
United States Evergreen Manor Everett Washington
United States Stanley Street Treatment and Resources (SSTAR) Fall River Massachusetts
United States Midtown Community Mental Health Center Indianapolis Indiana
United States The Center for Drug Free Living Orlando Florida
United States Hina Mauka Waipahu Hawaii
United States Project Outreach West Hempstead New York

Sponsors (2)

Lead Sponsor Collaborator
New York State Psychiatric Institute National Institute on Drug Abuse (NIDA)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Reduced Substance Use and Improved Treatment Retention Compared to patients assigned to Treatment as Usual (TAU), patients assigned to modified TAU plus the Therapeutic Education System (Modified TAU + TES) will have:
reduced substance use (measured by a combination of self-report confirmed by urine toxicology) and
better retention in treatment at their community-based treatment programs.
12-week Treatment Phase
Secondary Effectiveness To evaluate the relative effectiveness of TAU vs. modified TAU + TES on several secondary outcome measures, including measures of HIV risk behavior, psychosocial functioning (in areas of criminal activity, health status improvement, psychological status, family/social relationships, and employment, and treatment acceptability (based on participant feedback). 12-week treatment phase, 3- and 6-months post treatment
Secondary Sustained outcome To evaluate if improved substance use and retention outcomes are maintained 3- and 6-months post-intervention. 3- and 6-months post treatment
Secondary Economic Analysis To perform a comprehensive economic analysis of including TES in TAU to inform decisions regarding adoption of this new therapeutic tool (assessing incremental costs per increased abstinence time and quality adjusted life year). The economic analyses are clinically important, as even if the computerized intervention is shown to be effective, it may not be adopted in community-based treatment programs unless it is shown to be cost-effective due to the considerable financial constraints in such treatment settings. 12-week treatment phase, 3- and 6-months post treatment
Secondary Coping Skills To examine coping skills acquisition as a treatment process factor that may underlie changes observed during treatment. 12-week treatment phase, 3- and 6-months post treatment
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