- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00178776
A Transtheoretical Model Group Therapy for Cocaine
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Study Type
Enrollment (Actual)
Phase
- Phase 1
Contacts and Locations
Study Locations
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Texas
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Houston, Texas, United States, 77030
- University of Texas Houston Mental Sciences Institute
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
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
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 |
|---|---|
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Experimental: Transtheoretical Model Group
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Active Comparator: Education / Advice
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
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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.
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Secondary Outcome Measures
Outcome Measure |
|---|
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Secondary Outcome Measures Related to Cocaine and other Drug Use:
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1) Timeline Follow-Back (self-reported use / percent days
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abstinent)
|
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2) Cocaine Craving Worksheet (self report)
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3) Cocaine Negative Consequences Checklist (self report)
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4) Addiction Severity Index (ASI; Interviewer Administered)
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5) Blood Alcohol Breath (biological)
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6) Substance Use Report (self report)
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Secondary Outcome Measures Related to Feasibility of the Group Therapy:
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1) Participation / Attendance / Retention
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2) MI Scale (Therapist Adherence)
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3) Treatment Satisfaction Questionnaire
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4) Group Therapy Alliance Scale
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5) Group Atmosphere Scale
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6) Therapist Treatment Evaluation
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Secondary Outcome Measures Related to Psychiatric Symptoms:
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1) Beck Depression Inventory (BDI-II)
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2) Brief Symptom Inventory (BSI)
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Secondary Outcomes Related to Functioning:
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1) HIV Knowledge Questionnaire
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2) Risk Behavior Assessment
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3) SF-12
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Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Mary Marden Velasquez, Ph.D., University of Texas Houston Medical School, Dept. of Family & Community Medicine
Publications and helpful links
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
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
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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