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Behavioral Therapy Plus Naltrexone for Alcoholism

Comparison of Cognitive Behavioral Therapy and Motivational Enhancement Therapy Plus Naltrexone for Alcoholism

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00000456
Enrollment
160
Registered
1999-11-03
Start date
1992-09-30
Completion date
2002-08-31
Last updated
2010-10-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alcohol Dependence, Alcoholism

Keywords

Alcoholism, Alcohol Dependence, Naltrexone, Cognitive Behavioral Therapy

Brief summary

This study will compare cognitive behavioral therapy with a time-limited motivational enhancement therapy to which naltrexone (Revia) or placebo medication is added. In this randomized clinical trial, 160 alcohol-dependent outpatients, after 5 days of abstinence, will receive one of the two psychosocial therapies and either naltrexone (Revia) or placebo for a 12-week treatment period. Abstinence rates, alcohol use, and time to alcohol relapse will be evaluated in all four groups along with measures of alcohol craving, biological measures of alcohol consumption, drinking consequences, changes in self-confidence for avoiding alcohol, and medication compliance. All study participants will be assessed for measures of outcome variables at 3 and 6 months after completing the treatment protocol.

Interventions

BEHAVIORALcognitive behavior therapy
BEHAVIORALmotivational enhancement therapy

Sponsors

National Institute on Alcohol Abuse and Alcoholism (NIAAA)
CollaboratorNIH
Medical University of South Carolina
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
21 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Meets criteria for alcohol dependence, has not had more than one previous inpatient medical detoxification. * Consumes on average five standard drinks per day. * Able to maintain sobriety for five days (with or without the aid of detoxification medications) as determined by self-report, collateral report, and breathalyzer measurements. * Able to read and understand questionnaires and informed consent. * Lives within 50 miles of the study site.

Exclusion criteria

* Currently meets criteria for any other psychoactive substance dependency disorder. * Ever abused opiates. * Used psychoactive substance abuse, except marijuana, within the last 30 days as evidenced by patient report, collateral report, and urine drug screen. * Meets criteria for disorders of major depression, panic disorder, obsessive-compulsive disorder, post-traumatic stress syndrome, bipolar affective disorder, schizophrenia, or any other psychotic disorder or organic mental disorder. * Meets criteria for dissociate disorder or eating disorders. * Has current suicidal or homicidal ideation. * Need for maintenance or acute treatment with any psychoactive medication including antiseizure medications. * Current use of disulfiram (Antabuse). * Clinically significant medical problems that would impair participation or limit medication ingestion. * Hepatocellular disease. * Sexually active females of child bearing potential who are pregnant, nursing, or who are not using a reliable form of birth control. * Have current charges pending for a violent crime. * Does not have a stable living situation and a reliable source of collateral reporting. * Has taken an opiate antagonist drug in the last month.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 25, 2026