Will Having Alcohol Treatment Improve Functioning?

NCT ID: NCT01245647

Last Updated: 2018-05-07

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 19 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-11-30
• Study Completion Date: 2012-10-31

Brief Summary

The purpose of the study is to find out if a medication,naltrexone is helpful for HIV-infected women who sometimes drink too much. The study will try to find out whether women like the medication, whether the medication helps them cut back on their drinking, and whether it helps improve their overall health. Naltrexone has not been used widely among people who are engaged in less severe drinking and in primary health care settings. Therefore, the investigators would like to determine whether it is helpful among women who sometimes drink 4 or more drinks per occasion or 7 or more drinks per week. The investigators hypothesize that by taking naltrexone, women with hazardous drinking pattern will reduce their drinking which in turn will improve their medication adherence, improve their health and quality of life.

Detailed Description

The primary objective of this study is to evaluate the acceptability and effectiveness of a treatment program for hazardous drinking, delivered within HIV-clinic outpatient settings, that involves oral naltrexone. The central hypothesis is that women randomized to the treatment program will have decreased rates of hazardous drinking and improved clinical and behavioral health outcomes that are associated with hazardous drinking. The investigators have formulated this hypotheses based on the existing literature, the preliminary data and the clinical experience. The investigators hypothesize that women randomized to receive an alcohol treatment intervention will be less likely to have hazardous drinking behavior 6-months after enrollment, compared to women who received similar assessments but no formal treatment intervention. The investigators hypothesize that 4-months after enrollment, women randomized to receive an alcohol treatment intervention will have improved adherence to HIV antiretroviral therapy, improved CD4 cell counts, reduced HIV viral load, and reduced risky sexual behavior, compared to women who receive similar assessments but no formal intervention.

The investigators will recruit 90 women from 3 different sites in Florida, Washington DC and Chicago. Of those 90 women 60 will receive naltrexone and 30 will receive placebo. Study participants will take the medication for 4 months but the investigators will follow them for 7 months. At baseline, 2 months, 4 months and 7 months, the investigators will administer study questionnaires and assess their liver enzymes, CD4 count and viral load. The investigators will also follow them up at month 1 and 3 to reinforce the medication intake and to assess for any possible side effects.

New treatment options are available, but their impact on hazardous drinking has not yet been evaluated among HIV-infected women, many of whom are poor, minorities, or who have associated mental health or substance abuse problems. Delivery of therapeutic interventions must be improved in order to reduce hazardous drinking in women with HIV/AIDS. The proposed research is significant because the therapy will be offered within HIV clinic settings and will potentially improve the health of a population that is significantly undertreated. In addition to determining the effectiveness of an alcohol treatment intervention, the investigators will also identify key barriers and facilitators associated with adherence to pharmacologic treatment for alcohol in women with hazardous drinking. The findings will directly impact the type and quality of care for hazardous drinking in this subset of HIV-infected individuals and will inform both primary and secondary prevention efforts

Conditions

HIV; Alcoholism

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Sugar Pill, 50mg, once per day for 4 months

Placebo: One third of the participants will receive placebo pills that look the same as the active comparator but are really just inert pills. Each study participant will take a single pill once a day for 4 months.

Group Type: PLACEBO_COMPARATOR

Sugar pill, 50mg, once per day for 4 months

Intervention Type: OTHER

Placebo: One third of the participants will receive placebo pills that look the same as the active comparator but are really just inert pills. Each study participant will take a single pill once a day for 4 months.

Naltrexone, 50mg, once per day for 4 months

Naltrexone: Two thirds of the total study participants will receive the medication naltrexone. Each study participant will take a single pill once a day for 4 months.

Group Type: ACTIVE_COMPARATOR

Naltrexone, 50mg, once per day for 4 months

Intervention Type: DRUG

Naltrexone: Two thirds of the total study participants will receive the medication naltrexone. Each study participant will take a single pill once a day for 4 months.

Interventions

Naltrexone, 50mg, once per day for 4 months

Naltrexone: Two thirds of the total study participants will receive the medication naltrexone. Each study participant will take a single pill once a day for 4 months.

Intervention Type: DRUG

Sugar pill, 50mg, once per day for 4 months

Placebo: One third of the participants will receive placebo pills that look the same as the active comparator but are really just inert pills. Each study participant will take a single pill once a day for 4 months.

Intervention Type: OTHER

Other Intervention Names

Naltrexone; Inert sugar pill

Eligibility Criteria

Inclusion Criteria

• Hazardous drinking: defined by the NIAAA as either of the following:

1. binge drinking (4 or more drinks per occasion at least twice monthly), (NIAAA 2005) - OR

2. high quantity-frequency (>7 or drinks per week)

• Age 18 or over
• Female
• HIV-infected documented by a rapid HIV test or any licensed ELISA test kit and confirmed by a repeat ELISA, Western Blot, HIV-1 culture, HIV-1 antigen, plasma HIV-1 RNA viral load or a second antibody test by a method other than ELISA at any time prior to study entry.
• Able to understand and comply with planned study procedures.
• Willing and able to provide informed consent.

Exclusion Criteria

• Contraindications to treatment with naltrexone: current physiologic opiate dependence; current daily prescription opioid medications; positive urine drug test for opioids; allergic to naltrexone; significantly abnormal baseline liver enzymes (AST or ALT ≥ 5 times normal); on dialysis for renal failure
• currently taking oral medications for tuberculosis.
• Currently pregnant or positive pregnancy test.
• currently breastfeeding.
• Currently taking an alcohol treatment medication (disulfiram, topiramate, naltrexone, acamprosate).
• currently homeless, unable to provide mailing address, or has plans to move from area within next 7 months.
• Unable to communicate in English.
• Research coordinator assessment that participant cannot comprehend the study or consent procedures
• Has current prognosis of less than 1 year to live
• Abnormal vital signs at enrollment visit
• Currently on treatment for Hepatitis C (HCV) infection
• Prisoner status

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

National Institute on Alcohol Abuse and Alcoholism (NIAAA)

NIH

Sponsor Role: collaborator

University of Florida

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Robert L Cook, MD, MPH

Role: PRINCIPAL_INVESTIGATOR

University of Florida

Locations

Women's Interagency HIV Study

Washington D.C., District of Columbia, United States

University of Florida Health Science Center

Jacksonville, Florida, United States

Women's Interagency HIV Study

Chicago, Illinois, United States

Countries

United States

Other Identifiers

R01AA018934-01

Identifier Type: NIH

Identifier Source: secondary_id

View Link

AA018934-01-N

Identifier Type: -

Identifier Source: org_study_id