Reducing Unsafe Alcohol Use in HIV-Positive Individuals
Recruitment status was Recruiting
- Full Text View
- Tabular View
- No Study Results Posted
- Disclaimer
- How to Read a Study Record
Purpose
The main aim of this study is to test an intervention to reduce unsafe drinking among HIV-positive primary care patients. The intervention consists of a brief motivational interview, which is combined with daily alcohol monitoring through the use of an interactive voice response system IVR (automated telephone system). Subjects who receive the enhanced motivational interview are expected to show greater improvements in drinking than individuals who receive the standard motivational interview or view a DVD on HIV self-care.
| Condition | Intervention |
|---|---|
|
Alcohol Abuse |
Behavioral: Enhanced Motivational Interview Behavioral: Standard Motivational Interview or viewing DVD |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Reducing Unsafe Drinking in HIV Primary Care |
- Alcohol Consumption
- HIV Medication adherence
- HIV risk behavior
- HIV viral load (CD4 count)
- Liver enzymes/liver status (ALT, AST)
- Liver diseases (ALT, AST control variables)
- Depression (BDI score)
- Drug use
- Alcohol dependence
- Start of alcohol treatment/AA
- Start of hepatitis treatment if infected
| Estimated Enrollment: | 348 |
| Study Start Date: | October 2006 |
| Estimated Study Completion Date: | October 2011 |
| Estimated Primary Completion Date: | October 2011 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: 1 - enhanced MI
Enhanced brief motivational interview (including an IVR component for alcohol self-monitoring purposes)
|
Behavioral: Enhanced Motivational Interview
The intervention consists of a brief motivational interview, which is combined with daily alcohol monitoring through the use of an interactive voice response system IVR (automated telephone system).
|
|
Active Comparator: 2- standard MI
The intervention consists of a standard motivational interview or viewing a DVD on HIV self-care.
|
Behavioral: Standard Motivational Interview or viewing DVD
Brief motivational interview, viewing a DVD on HIV self-care.
|
Detailed Description:
HIV infection is a widespread health problem in the U.S. Antiretroviral treatment has increased longevity and changed the nature of risk factors for morbidity and mortality. Alcohol consumption has become an increasingly serious health issue among HIV primary care patients. Drinking is a key factor in progression to severe liver damage (especially those co-infected with hepatitis), and liver disease is now one of the most common causes of death among those with HIV. Excess drinking is also associated with medication noncompliance, reduces the effect of antiretroviral treatment, and is linked to other health problems. Therefore, helping HIV patients reduce unsafe drinking is crucial to their long-term health. The intervention combines the brief MI, an established, evidence-based counseling approach, with an innovative procedure designed to strengthen the effects of the MI. An effective, easily implemented alcohol-reduction intervention could be incorporated into standard care in HIV clinics helping prevent or slow the progress of some medical problems in HIV-infected individuals, improve medication compliance, prolong lifespan and decrease risk behavior associated with alcohol use.
Comparison(s): Enhanced brief motivational interview (including an IVR component for alcohol self-monitoring purposes), brief motivational interview, viewing a DVD on HIV self-care.
Eligibility| Ages Eligible for Study: | 18 Years to 65 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Male and females 18 years of age or older.
- Participants have had 4 or more drinks on any day in the prior 30 days assessed via standardized questions.
- Participants are referred to a study MI counselor by clinic staff as needing an intervention for drinking
- Participants agree to random assignment and provide informed consent
Exclusion Criteria:
- Participants who are currently psychotic, suicidal or homicidal.
- Participants who have definite plans to leave the greater New York metropolitan area within the study period.
- Participants who demonstrate gross cognitive impairment as evidenced on the Halstead-Reitain Trails (A).
- Participants who do not speak English or Spanish, or have hearing impairments that preclude use of the telephone.
Contacts and Locations| Contact: Deborah S. Hasin, PhD | 212-543-5035 | dsh2@columbia.edu |
| Contact: Efrat Aharonovich, PhD | 212-543-5035 | dsh2@columbia.edu |
| United States, New York | |
| New York State Psychiatric Institute/ St. Vincent's Hospital | Recruiting |
| New York, New York, United States, 10032 | |
| Contact: Deborah S. Hasin, PhD 212-543-5035 dsh2@columbia.edu | |
| Contact: Efrat Aharonovich, PhD 212-740-7257 ea2017@columbia.edu | |
| Principal Investigator: Deborah S. Hasin, PhD | |
| Sub-Investigator: Barbara E. Johnston, MD | |
| Sub-Investigator: David L. Kaufman, MD | |
| Study Director: | Selvija G. Marovic, PhD | New York State Psychiatric Institute (NYSPI) |
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00371969 History of Changes |
| Other Study ID Numbers: | NIAAA-HAS-14323, NIH Grant R01 AA14323-01A1 |
| Study First Received: | August 31, 2006 |
| Last Updated: | November 20, 2009 |
| Health Authority: | United States: Federal Government |
Keywords provided by National Institute on Alcohol Abuse and Alcoholism (NIAAA):
|
Unsafe drinking Human Immunodeficiency Virus Motivational Interviewing |
Additional relevant MeSH terms:
|
Alcoholism Alcohol-Related Disorders Substance-Related Disorders Mental Disorders |
ClinicalTrials.gov processed this record on May 23, 2013