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Web-delivery of Evidence-based, Psychosocial Treatment for Substance Use Disorders (CTN-0044)

Primary Purpose

Substance Abuse

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Therapeutic Education System (TES)
Treatment-as-Usual (TAU)
Sponsored by
New York State Psychiatric Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Substance Abuse focused on measuring Drug Abuse, Substance Abuse, Substance Use Disorder, Addiction, Behavioral Treatment

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

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.

Sites / Locations

  • MCCA: Midwestern CT Council on Alcoholism
  • The Center for Drug Free Living
  • Hina Mauka
  • Midtown Community Mental Health Center
  • HARBEL Prevention and Recovery Center
  • Stanley Street Treatment and Resources (SSTAR)
  • Project Outreach
  • Willamette Family, Inc.
  • Homeward Bound
  • Evergreen Manor

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Therapeutic Education System (TES)

Treatment-as-Usual (TAU)

Arm Description

Participants randomized to this arm will replace approximately 2 hours of Standard Treatment with the Therapeutic Education System (TES) (comprised of a web-based version of the Community Reinforcement Approach and contingency management).

Participants randomized to TAU will receive standard treatment offered and prescribed, as usual, in the outpatient substance abuse treatment program.

Outcomes

Primary Outcome Measures

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.

Secondary Outcome Measures

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).
Sustained outcome
To evaluate if improved substance use and retention outcomes are maintained 3- and 6-months post-intervention.
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.
Coping Skills
To examine coping skills acquisition as a treatment process factor that may underlie changes observed during treatment.

Full Information

First Posted
April 14, 2010
Last Updated
July 6, 2017
Sponsor
New York State Psychiatric Institute
Collaborators
National Institute on Drug Abuse (NIDA)
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1. Study Identification

Unique Protocol Identification Number
NCT01104805
Brief Title
Web-delivery of Evidence-based, Psychosocial Treatment for Substance Use Disorders
Acronym
CTN-0044
Official Title
NIDA-CTN-0044: Web-delivery of Evidence-Based, Psychosocial Treatment for Substance Use Disorders Using the Therapeutic Education System (TES)
Study Type
Interventional

2. Study Status

Record Verification Date
July 2017
Overall Recruitment Status
Completed
Study Start Date
April 2010 (undefined)
Primary Completion Date
June 2012 (Actual)
Study Completion Date
September 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
New York State Psychiatric Institute
Collaborators
National Institute on Drug Abuse (NIDA)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief 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.
Detailed 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Substance Abuse
Keywords
Drug Abuse, Substance Abuse, Substance Use Disorder, Addiction, Behavioral Treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
507 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Therapeutic Education System (TES)
Arm Type
Experimental
Arm Description
Participants randomized to this arm will replace approximately 2 hours of Standard Treatment with the Therapeutic Education System (TES) (comprised of a web-based version of the Community Reinforcement Approach and contingency management).
Arm Title
Treatment-as-Usual (TAU)
Arm Type
Other
Arm Description
Participants randomized to TAU will receive standard treatment offered and prescribed, as usual, in the outpatient substance abuse treatment program.
Intervention Type
Behavioral
Intervention Name(s)
Therapeutic Education System (TES)
Other Intervention Name(s)
Therapeutic Education System, TES
Intervention Description
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.
Intervention Type
Behavioral
Intervention Name(s)
Treatment-as-Usual (TAU)
Other Intervention Name(s)
Treatment as Usual, TAU, Standard Treatment
Intervention Description
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.
Primary Outcome Measure Information:
Title
Reduced Substance Use and Improved Treatment Retention
Description
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.
Time Frame
12-week Treatment Phase
Secondary Outcome Measure Information:
Title
Effectiveness
Description
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).
Time Frame
12-week treatment phase, 3- and 6-months post treatment
Title
Sustained outcome
Description
To evaluate if improved substance use and retention outcomes are maintained 3- and 6-months post-intervention.
Time Frame
3- and 6-months post treatment
Title
Economic Analysis
Description
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.
Time Frame
12-week treatment phase, 3- and 6-months post treatment
Title
Coping Skills
Description
To examine coping skills acquisition as a treatment process factor that may underlie changes observed during treatment.
Time Frame
12-week treatment phase, 3- and 6-months post treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
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.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Edward V Nunes, MD
Organizational Affiliation
NIDA Clinical Trials Network - Long Island Regional Node
Official's Role
Principal Investigator
Facility Information:
Facility Name
MCCA: Midwestern CT Council on Alcoholism
City
Danbury
State/Province
Connecticut
ZIP/Postal Code
06810
Country
United States
Facility Name
The Center for Drug Free Living
City
Orlando
State/Province
Florida
ZIP/Postal Code
32856
Country
United States
Facility Name
Hina Mauka
City
Waipahu
State/Province
Hawaii
ZIP/Postal Code
96797
Country
United States
Facility Name
Midtown Community Mental Health Center
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46208
Country
United States
Facility Name
HARBEL Prevention and Recovery Center
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21214
Country
United States
Facility Name
Stanley Street Treatment and Resources (SSTAR)
City
Fall River
State/Province
Massachusetts
ZIP/Postal Code
02720
Country
United States
Facility Name
Project Outreach
City
West Hempstead
State/Province
New York
ZIP/Postal Code
11552
Country
United States
Facility Name
Willamette Family, Inc.
City
Eugene
State/Province
Oregon
ZIP/Postal Code
97402
Country
United States
Facility Name
Homeward Bound
City
Dallas
State/Province
Texas
ZIP/Postal Code
75208
Country
United States
Facility Name
Evergreen Manor
City
Everett
State/Province
Washington
ZIP/Postal Code
98201
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
34366201
Citation
Luderer HF, Campbell ANC, Nunes EV, Enman NM, Xiong X, Gerwien R, Maricich YA. Engagement patterns with a digital therapeutic for substance use disorders: Correlations with abstinence outcomes. J Subst Abuse Treat. 2022 Jan;132:108585. doi: 10.1016/j.jsat.2021.108585. Epub 2021 Jul 30.
Results Reference
derived
PubMed Identifier
26880594
Citation
Murphy SM, Campbell AN, Ghitza UE, Kyle TL, Bailey GL, Nunes EV, Polsky D. Cost-effectiveness of an internet-delivered treatment for substance abuse: Data from a multisite randomized controlled trial. Drug Alcohol Depend. 2016 Apr 1;161:119-26. doi: 10.1016/j.drugalcdep.2016.01.021. Epub 2016 Jan 30.
Results Reference
derived
PubMed Identifier
25697725
Citation
Cochran G, Stitzer M, Campbell AN, Hu MC, Vandrey R, Nunes EV. Web-based treatment for substance use disorders: differential effects by primary substance. Addict Behav. 2015 Jun;45:191-4. doi: 10.1016/j.addbeh.2015.02.002. Epub 2015 Feb 8.
Results Reference
derived
PubMed Identifier
25671593
Citation
Mitchell SG, Schwartz RP, Alvanzo AA, Weisman MS, Kyle TL, Turrigiano EM, Gibson ML, Perez L, McClure EA, Clingerman S, Froias A, Shandera DR, Walker R, Babcock DL, Bailey GL, Miele GM, Kunkel LE, Norton M, Stitzer ML. The Use of Technology in Participant Tracking and Study Retention: Lessons Learned From a Clinical Trials Network Study. Subst Abus. 2015;36(4):420-6. doi: 10.1080/08897077.2014.992565. Epub 2015 Feb 11.
Results Reference
derived
PubMed Identifier
24708748
Citation
Cochran G, Stitzer M, Nunes EV, Hu MC, Campbell A. Clinically relevant characteristics associated with early treatment drug use versus abstinence. Addict Sci Clin Pract. 2014 Apr 4;9(1):6. doi: 10.1186/1940-0640-9-6.
Results Reference
derived
Links:
URL
http://www.drugabuse.gov/CTN/
Description
National Institute on Drug Abuse, Clinical Trials Network

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Web-delivery of Evidence-based, Psychosocial Treatment for Substance Use Disorders

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