A Transtheoretical Model Group Therapy for Cocaine

January 10, 2017 updated by: National Institute on Drug Abuse (NIDA)
The purpose of this study is to determine the feasibility and promise of a recently manualized group therapy based on the Transtheoretical Model for cocaine use disorders.

Study Overview

Detailed Description

Cocaine use in the general population is a significant and costly problem. Novel and innovative interventions targeting cocaine abuse are needed. The Transtheoretical Model of behavior change (TTM) offers a comprehensive framework for understanding, measuring, and intervening in behavior change and provides a strong theoretical foundation upon which effective treatments for substance abuse can be developed. The proposed Stage 1 research will pilot test a novel and innovative behavioral group therapy for cocaine users based on the TTM. In Phase 1, investigators will modify the newly developed Group Treatment for Substance Abuse: A Stages-of-Change Therapy Manual (Velasquez, Maurer, Crouch & DiClemente, 2001) to specifically target cocaine abuse resulting in a twelve-session, group intervention and accompanying therapy manual based on the TTM stages and processes of change: six "early stage" sessions targeting the experiential processes of change, and six "later stage" sessions targeting the behavioral processes of change. Phase 2 will consist of a pilot trial to evaluate the TTM group therapy with cocaine abusing patients. A randomized, controlled, between groups design will be used in which cocaine abusers (N=80) are assigned to one of two group treatment conditions: TTM therapy or Education/Advice. Participants will be recruited from Houston and surrounding communities through the Substance Abuse Research Center at the University of Texas Health Science Center Mental Sciences Institute. We expect the delivery of the TTM therapy for cocaine users to be feasible and acceptable, and to produce significant patient improvement. Cocaine outcomes will be assessed via objective (urine and drug analysis) and self-report measures. This Stage I research will contribute important theoretical and empirical information concerning the promise of a new and innovative intervention for cocaine abusers, and will provide the basis for a larger efficacy trial.

Study Type

Interventional

Enrollment (Actual)

138

Phase

  • Phase 1

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Texas
      • Houston, Texas, United States, 77030
        • University of Texas Houston Mental Sciences Institute

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

Inclusion Criteria: Male and female adults (ages 18-65 years old), of any race, who meet DSM-IV criteria for cocaine abuse or dependence disorder will be recruited. In addition, eligible participants must be:

  • (1) judged to be in generally good physical and psychiatric health except for possible acute drug related problems;
  • (2) willing and able to participate in the 6-week, group outpatient treatment;
  • (3) able to provide the name of at least one person who can generally locate their whereabouts; and
  • (4) willing to be followed for 3 months after treatment ends.

Potential subjects with simple drug charges whose legal contacts are willing to forego data revelation will be included. Although cocaine dependence will be the primary drug for which patients are seeking treatment, we will not exclude participants who are abusing additional substances.

Exclusion Criteria:

Individuals will be ineligible for study participation based on the following criteria:

  • (1) current diagnosis of an Axis I psychiatric disorder other than cocaine dependence;
  • (2) current psychiatric symptoms requiring medication;
  • (3) severe medical, cognitive and /or psychiatric impairment that precludes cooperation with study protocol;
  • (4) substance withdrawal symptoms requiring medical attention;
  • (5) currently receiving other psychosocial therapy for substance abuse with the exception of AA, NA or CA;
  • (6) impending incarceration;
  • (7) inability to read, write, speak English;
  • (8) inability or unwillingness to participate in the 6-week, group outpatient treatment (e.g., halfway house or other aftercare program restrictions).

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: RANDOMIZED
  • Interventional Model: PARALLEL
  • Masking: DOUBLE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Transtheoretical Model Group
Active Comparator: Education / Advice

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Urinalysis indicating presence or absence of cocaine metabolites, used to calculate percent days abstinent, collected at intake, once weekly during the 6 week group treatment phase, at post-treatment, and 3 months.

Secondary Outcome Measures

Outcome Measure
Secondary Outcome Measures Related to Cocaine and other Drug Use:
1) Timeline Follow-Back (self-reported use / percent days
abstinent)
2) Cocaine Craving Worksheet (self report)
3) Cocaine Negative Consequences Checklist (self report)
4) Addiction Severity Index (ASI; Interviewer Administered)
5) Blood Alcohol Breath (biological)
6) Substance Use Report (self report)
Secondary Outcome Measures Related to Feasibility of the Group Therapy:
1) Participation / Attendance / Retention
2) MI Scale (Therapist Adherence)
3) Treatment Satisfaction Questionnaire
4) Group Therapy Alliance Scale
5) Group Atmosphere Scale
6) Therapist Treatment Evaluation
Secondary Outcome Measures Related to Psychiatric Symptoms:
1) Beck Depression Inventory (BDI-II)
2) Brief Symptom Inventory (BSI)
Secondary Outcomes Related to Functioning:
1) HIV Knowledge Questionnaire
2) Risk Behavior Assessment
3) SF-12

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Mary Marden Velasquez, Ph.D., University of Texas Houston Medical School, Dept. of Family & Community Medicine

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

  • Velasquez, M. M., Maurer, G. G., Crouch, C., & DiClemente, C. C. (2001). Group treatment for substance abuse: A stages-of-change therapy manual. New York: Guilford Press.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

October 1, 2003

Primary Completion (Actual)

November 1, 2006

Study Completion (Actual)

June 1, 2007

Study Registration Dates

First Submitted

September 13, 2005

First Submitted That Met QC Criteria

September 13, 2005

First Posted (Estimate)

September 15, 2005

Study Record Updates

Last Update Posted (Estimate)

January 11, 2017

Last Update Submitted That Met QC Criteria

January 10, 2017

Last Verified

September 1, 2014

More Information

Terms related to this study

Other Study ID Numbers

  • 5R01DA015453-02 (U.S. NIH Grant/Contract)
  • R01DA015453-02 (U.S. NIH Grant/Contract)
  • UT CPHS ID - HSC-MS-02-138 (Other Identifier: University of Texas Health Science Center Houston)

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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