HIV and Alcohol Research Center Focused on Polypharmacy (HARP)

Sponsor
Yale University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05560932
Collaborator
National Institute on Alcohol Abuse and Alcoholism (NIAAA) (NIH)
50
1
3

Study Details

Study Description

Brief Summary

This pilot intervention will consist of a brief intervention for patients with HIV who take 5 or more medications and currently (within the past month) consume alcohol. The focus of this pilot will be on bothersome symptoms and the impact of alcohol use and medications on these symptoms. The rationale is that any alcohol use may interact with medications in serious ways leading to adverse outcomes, including bothersome symptoms.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: IMB-motivational interviewing (MI) techniques (IMB-MI)
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
HIV and Alcohol Research Center Focused on Polypharmacy (HARP)
Anticipated Study Start Date :
Jan 1, 2023
Anticipated Primary Completion Date :
Mar 1, 2023
Anticipated Study Completion Date :
Apr 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: HIV Medications and Alcohol Use

Participants with HIV who take 5 or more medications and currently (within the past month) consume alcohol

Behavioral: IMB-motivational interviewing (MI) techniques (IMB-MI)
The clinical pharmacist will employ MI in informational, participant-centered discussions in which the clinical pharmacist and participant collaboratively discuss the harms of drinking and polypharmacy (specifically alcohol interactive medications), symptoms associated with alcohol and specific medications, and how to mitigate these harms. Motivational elements include messages highlighting the participant's personal risk of bothersome symptoms from their use of alcohol and level of polypharmacy, attitude change elements to improve attitudes toward the intended behavior change, social normative support for the intended behavior change including identification of people who can support the participant in this process, and a menu of options for referrals for skill building (e.g. Social Work, meeting with the clinical pharmacist at their clinic, follow-up with the HIV clinician, alcohol-reduction programs, based on what is locally available as part of VA-based care).

Outcome Measures

Primary Outcome Measures

  1. Change in Bothersome Symptoms from baseline using the HIV Symptoms Index [baseline, immediately post-intervention, 30 days post intervention]

    The HIV Symptoms Index is a 20-item, self-reported measure that assesses presence and perceived distress linked to symptoms associated with HIV or HIV treatment. There are 5 possible responses: 0 = I don't have this symptom; 1 = It doesn't bother me; 2 = It bothers me a little; 3 = It bothers me; and 4 = It bothers me a lot, for each HIV symptom. Total score is derived by counting the number of bothersome symptoms.

  2. Change in Phosphatidylethanol (PEth) Levels [baseline and 30 days post intervention]

    Change in alcohol levels assessed measuring PEth levels in the blood. PEth testing uses blood to measure alcohol use by detecting direct alcohol biomarkers in the bloodstream. A positive test indicates alcohol use.

  3. Number of Medications Prescribed Post Intervention [baseline and 30 days post intervention]

    The number of prescriptions prescribed post intervention will be assessed by phone contact, paper survey and electronic health record pharmacy data.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • participants in both Veterans Aging Cohort Study (VACS) and Medications, Alcohol, and Substance use in HIV (MASH) studies

  • prescribed 5 or more medications AND who either have a positive PEth value (8+) or a self-reported AUDIT-C value consistent with current alcohol use (score >0)

Exclusion Criteria:
  • Alcohol use disorder (AUD) diagnosis in the past 12 months or who test positive for AUD on the Alcohol Symptom Checklist for moderate or severe AUD (score of 4 or more)

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Yale University
  • National Institute on Alcohol Abuse and Alcoholism (NIAAA)

Investigators

  • Principal Investigator: Amy C Justice, MD, PhD, Yale University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Yale University
ClinicalTrials.gov Identifier:
NCT05560932
Other Study ID Numbers:
  • Justice 090622
  • P01AA029545
First Posted:
Sep 30, 2022
Last Update Posted:
Dec 5, 2022
Last Verified:
Dec 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 5, 2022