Cognitive Enhancement and Relapse Prevention in Cocaine Addiction
Primary Purpose
Cocaine Addiction
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Seromycin (D-cycloserine, DCS)
Placebo
Computerized Cognitive Behavioral Therapy
Sponsored by
About this trial
This is an interventional treatment trial for Cocaine Addiction focused on measuring cocaine dependence, relapse prevention, computerized cognitive behavioral therapy (CBT), D-cycloserine (DCS)
Eligibility Criteria
Inclusion Criteria:
- Eligible subjects must be cocaine-dependent persons between 18 and 65 years
Exclusion Criteria:
- Any current Axis-I psychiatric diagnosis other than cocaine or alcohol dependence or nicotine use
- Any current or prior neurological disease, history of a major medical illness, or current use of psychotropic medications
- Positive history of loss of consciousness of greater than 10 min
- Significant current or prior cardiovascular disease (hypertension, arrhythmias) that is not medically stable
- History of hospitalization within the previous six months for a medical illness
- Deafness, blindness or other significant sensory impairment.
- Contraindications for D-cycloserine and magnetic resonance imaging.
Sites / Locations
- Psychiatric Research Institute (PRI) (Center for Addiction Research (CAR) and Brain Imaging Research Center (BIRC)) University of Arkansas for Medical Sciences
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
DCS and Cognitive Behavioral Therapy
Placebo and Cognitive Behavioral Therapy
Arm Description
Subjects will receive 250 mg of Seromycin or D-cycloserine (DCS) prior to computerized cognitive behavioral therapy.
Subjects will receive a 250 mg identical looking placebo pill prior to computerized cognitive behavioral therapy.
Outcomes
Primary Outcome Measures
Drug Abstinence During Treatment and at Follow up Visits
Percentage of the overall number of drug abstinences of participants measured by urine drug testing
Treatment Retention - Number of Visits During Treatment
Number of treatment visits attended prior to discontinuation of treatment
Secondary Outcome Measures
Full Information
NCT ID
NCT01067846
First Posted
February 10, 2010
Last Updated
October 31, 2013
Sponsor
University of Arkansas
Collaborators
National Institute on Drug Abuse (NIDA)
1. Study Identification
Unique Protocol Identification Number
NCT01067846
Brief Title
Cognitive Enhancement and Relapse Prevention in Cocaine Addiction
Official Title
The Clinical and Neural Response of Cocaine Addicts to Combination Treatment With a Cognitive Enhancer and Extinction-Based Psychotherapy
Study Type
Interventional
2. Study Status
Record Verification Date
October 2013
Overall Recruitment Status
Completed
Study Start Date
June 2010 (undefined)
Primary Completion Date
January 2012 (Actual)
Study Completion Date
January 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Arkansas
Collaborators
National Institute on Drug Abuse (NIDA)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
For this project, the investigators are interested in exploring a new way to extend and maintain drug abstinence in people who are addicted to crack cocaine. This study will combine a medication called D-Cycloserine (DCS) and weekly cognitive behavioral therapy (CBT) to assess whether the combination will enhance people's ability to stay clean (drug free) for longer periods of time.
One of the greatest risks for drug relapse is drug craving. Oftentimes drug craving occurs when a person is confronted with stressors and reminders of past drug use behavior. DCS has been shown to enhance the learning of new information. By administering DCS prior to learning new techniques such as how to cope with drug craving and drug-use reminders, it is possible that patients can be more successful at living a drug free life for a longer period of time.
In addition to exploring this model behaviorally, the investigators will explore changes that may occur in the brain before and after the therapy/medication intervention. A technique called MRI (Magnetic Resonance Imaging) will be used to identify areas of the brain that are being activated during an attention task. Areas of neural activation will be assessed at study entry, end of therapy (4-week endpoint) and one month following completion of the treatment program.
Detailed Description
Primary Hypothesis:
Enhancing glutamatergic neurotransmission with DCS facilitates CBT-related relapse prevention by potentiating the behavioral and neural representation of the diminished drug motivation associated with cocaine cues.
Specific Aims:
Determine if the short-term oral administration of DCS relative to placebo prior to CBT sessions facilitates cocaine abstinence and functional recovery, and reduces cocaine craving in treatment-seeking cocaine addicts.
Determine if DCS administration relative to placebo facilitates CBT-related decreases in the behavioral and neural response to conditioned cocaine cues.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cocaine Addiction
Keywords
cocaine dependence, relapse prevention, computerized cognitive behavioral therapy (CBT), D-cycloserine (DCS)
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
85 (Actual)
8. Arms, Groups, and Interventions
Arm Title
DCS and Cognitive Behavioral Therapy
Arm Type
Experimental
Arm Description
Subjects will receive 250 mg of Seromycin or D-cycloserine (DCS) prior to computerized cognitive behavioral therapy.
Arm Title
Placebo and Cognitive Behavioral Therapy
Arm Type
Placebo Comparator
Arm Description
Subjects will receive a 250 mg identical looking placebo pill prior to computerized cognitive behavioral therapy.
Intervention Type
Drug
Intervention Name(s)
Seromycin (D-cycloserine, DCS)
Other Intervention Name(s)
D-cycloserine, DCS
Intervention Description
250 mg DCS once weekly for 4 weeks prior to the initiation of a Computerized Cognitive Behavioral Therapy (CBT) session for drug relapse intervention.
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Placebo identical looking to the 250 mg DCS once weekly for 4 weeks prior to the initiation of a Computerized Cognitive Behavioral Therapy (CBT) session for drug relapse intervention.
Intervention Type
Behavioral
Intervention Name(s)
Computerized Cognitive Behavioral Therapy
Intervention Description
All participants received Computerized Cognitive Behavioral Therapy sessions 3 times per week for 4 weeks as a drug relapse intervention.
Primary Outcome Measure Information:
Title
Drug Abstinence During Treatment and at Follow up Visits
Description
Percentage of the overall number of drug abstinences of participants measured by urine drug testing
Time Frame
Participants provided urine samples for drug testing during treatment which occurred 3 times per week for 4 weeks, at the end of treatment, and at a 1 and 2 month follow up visit
Title
Treatment Retention - Number of Visits During Treatment
Description
Number of treatment visits attended prior to discontinuation of treatment
Time Frame
Treatment sessions included 3 visits per week for 4 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Eligible subjects must be cocaine-dependent persons between 18 and 65 years
Exclusion Criteria:
Any current Axis-I psychiatric diagnosis other than cocaine or alcohol dependence or nicotine use
Any current or prior neurological disease, history of a major medical illness, or current use of psychotropic medications
Positive history of loss of consciousness of greater than 10 min
Significant current or prior cardiovascular disease (hypertension, arrhythmias) that is not medically stable
History of hospitalization within the previous six months for a medical illness
Deafness, blindness or other significant sensory impairment.
Contraindications for D-cycloserine and magnetic resonance imaging.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Clinton Kilts, PhD
Organizational Affiliation
University of Arkansas
Official's Role
Principal Investigator
Facility Information:
Facility Name
Psychiatric Research Institute (PRI) (Center for Addiction Research (CAR) and Brain Imaging Research Center (BIRC)) University of Arkansas for Medical Sciences
City
Little Rock
State/Province
Arkansas
ZIP/Postal Code
72205
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Cognitive Enhancement and Relapse Prevention in Cocaine Addiction
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