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OpenTrials
Active, Not Recruiting

NCT Number: NCT06006143

Off-Label Medications for Alcohol Use Disorder Among Patients With HIV: Pilot Study 2

This study seeks to determine the feasibility, acceptability, and preliminary efficacy of an intervention consisting of off-label use of a medication with strong efficacy data for alcohol use disorder (AUD) with medical management and a clinical pharmacist-delivered behavioral intervention in reducing alcohol use among individuals with HIV and AUD.

Active, Not Recruiting

This study is active but is not currently recruiting participants.

Key information

About this study

This is a series of three open-label pilot studies that consist of a 12-week intervention including off-label use of medication with MM and a clinical pharmacist-delivered behavioral intervention to treat AUD. Participants will receive counseling that incorporates brief feedback and advice with motivational enhancement techniques to assist the participant in changing their behaviors with respect to alcohol consumption and/or polypharmacy defined as taking five or more medications, particularly if those medications interact with alcohol. In addition, participants will be offered varenicline in the first pilot study. The rationale for utilizing an open-label pilot study design is to determine the feasibility, acceptability, safety, and preliminary efficacy of this intervention for the management of AUD. Participants will be interviewed with regards to their perspectives on feasibility and acceptability. They will be instructed to have medication bottles at study visits to assess medication adherence and will be assessed with readiness to change metrics and questions regarding quantity and frequency of alcohol use. Patients will also be asked to complete an AUDIT-C screen and the Alcohol Symptom Checklist at the start of the study period to screen for mild, moderate, or severe AUD. Several assessments including interviews and laboratory testing will be done at study visits.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • diagnosed with HIV
  • Receive care at the Atlanta VA Healthcare System
  • Are age 18 or over
  • Meet criteria for mild, moderate, or severe alcohol use disorder by the DSM-5 Alcohol Symptom Checklist and the Alcohol Use Disorders Identification Test-Consumption (AUDIT-C) screen
  • Have evidence of significant alcohol use: PEth > 20ng/ml
  • Currently smoking cigarettes
  • Prescribed >=5 medications
  • Have cell phone or reliable contact number
  • Can provide written informed consent

Exclusion criteria

  • Active engagement in formal alcohol treatment including medications for alcohol use disorder at the time of enrollment
  • Self-report or laboratory test confirming pregnancy, nursing, or trying to conceive
  • Life-threatening or unstable medical, surgical, or psychiatric condition that prohibits participation (including current or past intent to harm oneself or others within the prior 12 months and not receiving treatment
  • Untreated moderate to severe opioid use disorder
  • Residence out of state
  • Inability to read or understand English
  • History of serious hypersensitivity or adverse reaction to study medication
  • Taking potentially interactive medication(s) (e.g. nicotine replacement therapy for varenicline pilot study)
  • Already prescribed the pilot medication at the time of study recruitment

Treatment and study plan

Varenicline

Drug

All participants will receive a prescription for varenicline and will meet with a clinical pharmacist and addiction psychiatrist for further support

Primary outcomes

  1. Proportion of participants who complete enrollment and duration of sessions

    Time frame: 12 weeks

    Proportion of participants who complete enrollment and duration of sessions to assess feasibility of study

  2. Number of sessions completed

    Time frame: 12 weeks

    Number of sessions completed to assess acceptability of study

  3. Adherence to Medication

    Time frame: 12 weeks

    Medication adherence will be measured by the number of prescriptions filled by electronic health record to assess acceptability of study

  4. Safety of study assessed by adverse events reporting

    Time frame: 12 weeks

    Safety will be assessed by the percentage of study participants who report adverse events

Secondary outcomes

  1. Efficacy of study - change in self-reported alcohol use

    Time frame: 12 weeks

    Change in self-reported alcohol use (# of days of alcohol use and # of drinks per day) on the Timeline Followback.

  2. Efficacy of study - change in PEth (phosphatidylethanol) results

    Time frame: 12 weeks

    PEth is a biomarker for alcohol consumption. Change in PEth result from baseline PEth levels.

Sponsors and collaborators

Lead sponsor

Yale University

Other

Collaborators

  • National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Registry information

Official study title

Feasibility, Acceptability, and Preliminary Efficacy of Off-Label Medications for Alcohol Use Disorder Among Patients With HIV: An Open-Label Pilot Study

Acronym: HARP

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Aug 23, 2023
Registry last updated
Apr 16, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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