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Integrating Combined Therapies for Persons With Co-occurring Disorders (ICT)

Primary Purpose

Alcohol Use Disorder, Mental Health Disorder

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Integrating Combined Therapies
Standard Care
Sponsored by
Stanford University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Alcohol Use Disorder focused on measuring Integrating Combined Therapies, Alcohol Use Disorder, Mental Health Disorder

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. At least 18 years old;
  2. Evaluated and admitted to outpatient addiction treatment services at RMHS Evergreen program and meets criteria for any alcohol or substance use disorder;
  3. Screened positive for an alcohol problem on the Alcohol Use Disorders Identification Test (AUDIT) (score of 8 or higher) (screening instrument);
  4. Screened positive for a mental health problem on the Modified MINI Screen (MMS) (score of 6 or higher) (screening instrument);
  5. Diagnoses confirmed by SCID (diagnostic interview); AND
  6. Willing and able to provide informed consent.

Exclusion Criteria:

  1. They have acute psychotic symptoms and are not appropriately connected with mental health services;
  2. They have had a psychiatric hospitalization or suicide attempt within the past month (however, if the hospitalization or attempt was directly related to substance intoxication or detoxification and the person is currently stable, they are eligible); OR
  3. They have unstable medical or legal situations that would make participation for the full duration of the study highly unlikely.

Sites / Locations

  • Evergreen - Rutland Mental Health

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Integrating Combined Therapies

Standard Care

Arm Description

Integrating Combined Therapies (ICT) is a 10-session, manual-guided individual therapy. ICT has three phases designed to address substance use, psychiatric problems and their interactions. MET is the first phase (2 sessions) and is focused on assessment, feedback and securing motivation to address problems and take steps. CBT is the second phase (5 sessions) and incorporates patient education and functional analysis, develops coping skills, teaches methods to challenge beliefs, and activates alternative behaviors. TSF (3 sessions) is focused on maintaining recovery and engaging in community-based recovery activities. Although ICT has core components, its application is flexible to accommodate the unique needs and problems of individual patients (and their comorbidities).

Standard Care (SC) is the typical outpatient treatment that the patient would receive ordinarily at the identified addiction treatment program. SC service operates using the American Society of Addiction Medicine criteria (9 hours per week); group and individual sessions focused on motivation to address substance use, education about the consequences of substance use on major life areas, education about the disease concept and brain changes associated with addiction, exposure to information about social and family relationships and recovery, and relapse prevention skills.

Outcomes

Primary Outcome Measures

Decrease from baseline in alcohol use (90-day Timeline Follow Back (TLFB) at 4-months and at 7-months
Decrease from baseline in alcohol use severity (ASI; alcohol severity composite) at 4-months and at 7-months
Decrease from baseline in alcohol use severity (Short Inventory of Problems (SIP)) at 4-months and at 7-months
Decrease from baseline in psychiatric symptom severity (ASI; Psychiatric Severity Composite) at 4-months and at 7-months
Decrease in psychiatric symptom severity (Brief Symptom Inventory (BSI)) at 4-months and 7-months

Secondary Outcome Measures

Decrease from baseline in drug use (90-day TLFB) at 4-months and at 7-months
Decrease from baseline in positive toxicology screen (urine drug screen) at 4-months and at 7-months
Decrease from baseline in drug use severity (ASI; Drug Severity Composite) at 4-months and 7-months

Full Information

First Posted
October 27, 2015
Last Updated
June 28, 2018
Sponsor
Stanford University
Collaborators
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
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1. Study Identification

Unique Protocol Identification Number
NCT02598518
Brief Title
Integrating Combined Therapies for Persons With Co-occurring Disorders
Acronym
ICT
Official Title
Integrating Combined Therapies for Persons With Co-occurring Disorders
Study Type
Interventional

2. Study Status

Record Verification Date
June 2018
Overall Recruitment Status
Completed
Study Start Date
July 2015 (undefined)
Primary Completion Date
September 30, 2017 (Actual)
Study Completion Date
December 31, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Stanford University
Collaborators
National Institute on Alcohol Abuse and Alcoholism (NIAAA)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to assess the effectiveness and implementability of ICT for co-occurring alcohol use and mental health disorders within community addiction treatment, as delivered by routine community addiction clinicians.
Detailed Description
The proposed study will evaluate the effectiveness and implementability of a manual-guided integrated psychosocial treatment, Integrating Combined Therapies (ICT). ICT is an adaptation of the Combined Behavioral Intervention (CBI) from NIAAA Project COMBINE, and expands CBI's indication for alcohol problems to extend to drug use and the most common psychiatric problems in addiction treatment. ICT is designed to be transferable to routine care settings and for delivery by the existing workforce. Findings from a 2014 study provide a signal for ICT effectiveness and implementation. We intend to randomly assign 76 eligible patients in outpatient addiction treatment to ICT adapted standard care (ICT+SC) versus standard care only (SC). There are 2 specific aims for this study: Aim 1: Relative to standard care alone, to evaluate if patients receiving ICT have more significant reductions in alcohol use and severity as measured by the 90-day Timeline Follow Back (TLFB), Addiction Severity Index (ASI), and Short Inventory of Problems (SIP). Aim 2: Relative to standard care alone, to evaluate if patients receiving ICT have more significant reductions in psychiatric symptom severity, as measured by the Brief Symptom Inventory (BSI) adn the ASI psychiatric severity composite. This study involves a two-group repeated measure design. This study is a randomized controlled trial. The investigators plan to examine the outcomes associated with ICT versus standard care among patients receiving outpatient addiction treatment services. The investigators will employ assessments at baseline, four-month follow-up, and seven-month follow-up. Eligible participants will be randomly assigned to ICT therapy (plus standard care) or standard care, and all will be followed for the research assessments regardless of whether they drop out of treatment early (whenever possible). Patients admitted to the participating addiction treatment program are routinely screened for an alcohol use disorder using the AUDIT and a mental health disorder using the MMS. These forms are collected by clinic staff and scored for alcohol use disorder (AUDIT: 8 or greater) and mental health disorder (MMS: 6 or greater). Patients meeting the threshold criteria on the AUDIT and MMS measures are approached by clinic staff about potential interest in the study. If they wish to learn more about the study, the research assistant is contacted, a suitable time is arranged, and the patient engaged in the process of informed consent. If consent is granted, the participant completes the baseline assessment. The baseline assessment consists of measures gathered via interview by a member of the research team, self-administered surveys completed directly by the participant, and review of the participant's medical record to extract substance use, treatment history, and chart diagnoses. The interview portion of the assessment consists of : Standardized interview designed to assess mental health diagnoses: Structured Clinical Interview for DSM5 (SCID). A urine screen and breathalyzer to test for alcohol and other drugs. Standardized follow-back method for gathering data on recent alcohol and drug use: Timeline Follow-back calendar (TLFB) The self-administered portion of the assessment consists of measures designed to assess: Alcohol and drug use, as well as associated problems in other life areas such as medical, employment, legal, social, and psychiatric: Addiction Severity Index Psychiatric symptoms: Brief Symptom Inventory (BSI) Mental health disorders: Modified MINI Screen (MMS) Negative consequences of alcohol and substance use: Short Inventory of Problems- Alcohol and Drugs (SIP-AD) Substance use symptoms and problems: Brief Addiction Monitor (BAM) Treatment utilization: Recent Treatment Survey (RTS) If the participant continues to meet criteria for a mental health disorder (i.e. SCID interview confirms diagnosis of DSM5 mental health disorder, he or she is randomized to receive the study ICT therapy or standard care (SC) Research assessments are then also conducted at four months and seven months post baseline assessment. The follow-up assessments will consist of the same measures administered at baseline, with the exception of the SCID interview. The investigators plan to randomize approximately 76 participants in the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alcohol Use Disorder, Mental Health Disorder
Keywords
Integrating Combined Therapies, Alcohol Use Disorder, Mental Health Disorder

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Integrating Combined Therapies
Arm Type
Experimental
Arm Description
Integrating Combined Therapies (ICT) is a 10-session, manual-guided individual therapy. ICT has three phases designed to address substance use, psychiatric problems and their interactions. MET is the first phase (2 sessions) and is focused on assessment, feedback and securing motivation to address problems and take steps. CBT is the second phase (5 sessions) and incorporates patient education and functional analysis, develops coping skills, teaches methods to challenge beliefs, and activates alternative behaviors. TSF (3 sessions) is focused on maintaining recovery and engaging in community-based recovery activities. Although ICT has core components, its application is flexible to accommodate the unique needs and problems of individual patients (and their comorbidities).
Arm Title
Standard Care
Arm Type
Active Comparator
Arm Description
Standard Care (SC) is the typical outpatient treatment that the patient would receive ordinarily at the identified addiction treatment program. SC service operates using the American Society of Addiction Medicine criteria (9 hours per week); group and individual sessions focused on motivation to address substance use, education about the consequences of substance use on major life areas, education about the disease concept and brain changes associated with addiction, exposure to information about social and family relationships and recovery, and relapse prevention skills.
Intervention Type
Behavioral
Intervention Name(s)
Integrating Combined Therapies
Other Intervention Name(s)
ICT
Intervention Description
Individual Integrating Combined Therapies, approximately 10 sessions, one session per week
Intervention Type
Behavioral
Intervention Name(s)
Standard Care
Other Intervention Name(s)
SC
Intervention Description
Standard Care, individual or group therapy, approximately 9 hours per week for 3 months.
Primary Outcome Measure Information:
Title
Decrease from baseline in alcohol use (90-day Timeline Follow Back (TLFB) at 4-months and at 7-months
Time Frame
Baseline, 4-month, 7-month follow-up
Title
Decrease from baseline in alcohol use severity (ASI; alcohol severity composite) at 4-months and at 7-months
Time Frame
Baseline, 4-month, 7-month follow-up
Title
Decrease from baseline in alcohol use severity (Short Inventory of Problems (SIP)) at 4-months and at 7-months
Time Frame
Baseline, 4-month, 7-month follow-up
Title
Decrease from baseline in psychiatric symptom severity (ASI; Psychiatric Severity Composite) at 4-months and at 7-months
Time Frame
Baseline, 4-month, 7-month follow-up
Title
Decrease in psychiatric symptom severity (Brief Symptom Inventory (BSI)) at 4-months and 7-months
Time Frame
Baseline, 4-month, 7-month follow-up
Secondary Outcome Measure Information:
Title
Decrease from baseline in drug use (90-day TLFB) at 4-months and at 7-months
Time Frame
Baseline, 4-month, 7-month follow-up
Title
Decrease from baseline in positive toxicology screen (urine drug screen) at 4-months and at 7-months
Time Frame
Baseline, 4-month, 7-month follow-up
Title
Decrease from baseline in drug use severity (ASI; Drug Severity Composite) at 4-months and 7-months
Time Frame
Baseline, 4-month, 7-month follow-up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: At least 18 years old; Evaluated and admitted to outpatient addiction treatment services at RMHS Evergreen program and meets criteria for any alcohol or substance use disorder; Screened positive for an alcohol problem on the Alcohol Use Disorders Identification Test (AUDIT) (score of 8 or higher) (screening instrument); Screened positive for a mental health problem on the Modified MINI Screen (MMS) (score of 6 or higher) (screening instrument); Diagnoses confirmed by SCID (diagnostic interview); AND Willing and able to provide informed consent. Exclusion Criteria: They have acute psychotic symptoms and are not appropriately connected with mental health services; They have had a psychiatric hospitalization or suicide attempt within the past month (however, if the hospitalization or attempt was directly related to substance intoxication or detoxification and the person is currently stable, they are eligible); OR They have unstable medical or legal situations that would make participation for the full duration of the study highly unlikely.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark P. McGovern, Ph.D.
Organizational Affiliation
Stanford University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Evergreen - Rutland Mental Health
City
Rutland
State/Province
Vermont
ZIP/Postal Code
05701
Country
United States

12. IPD Sharing Statement

Learn more about this trial

Integrating Combined Therapies for Persons With Co-occurring Disorders

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