Actively Recruiting

Phase Not Applicable
Age: 35Years - 70Years
All Genders
ID05153811

Novel Extensions of Alcohol Contingency Management in People Living With HIV

Led by University of Florida · Updated on 2025-07-31

120

Participants Needed

2

Research Sites

N/A

Total Duration

On this page

Sponsors

U

University of Florida

Lead Sponsor

U

University of Miami

Collaborating Sponsor

AI-Summary

What this Trial Is About

Researchers are studying new ways to use Contingency Management (CM) combined with mobile health (mHealth) tools to help people living with HIV reduce their alcohol use. This study focuses on using a smartphone breathalyzer device paired with an app and a wrist-worn alcohol biosensor to encourage participants to drink less. The goal is to understand how these innovative tools can support alcohol reduction among adults living with HIV. Participants will be part of one of three groups, all involving wearing a wrist biosensor and using a smartphone breathalyzer. During the first 30 days, all will receive daily CM based on breathalyzer readings. In the next 30 days, the groups differ: one group receives encouragement without payment based on drinking, another receives weekly CM based on biosensor readings and interacts with a mobile app designed to gamify drinking reduction, and the third group receives weekly CM based on biosensor readings without the app. Brief counseling providing personalized feedback on alcohol levels and cognitive and physical functioning is also part of the interventions. During the study, participants will be monitored using biosensor and breathalyzer readings to track alcohol use and abstinence. Researchers will assess how many days participants remain abstinent from alcohol, their responses to CM strategies, and how these relate to other non-drinking outcomes. The study includes follow-up assessments up to six months to evaluate the lasting effects of the intervention. Participants' ease of use and perceived value of the contingency management strategies will also be evaluated, with safety monitored by exclusion of individuals with severe psychiatric conditions or recent intensive addiction treatment.

CONDITIONS

Brief Title

The Less is More Study

Who Can Participate

Age: 35Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Frequent alcohol use in the past 30 days based on Timeline Followback responses
  • HIV positive
  • Fluent in English
  • Willing to attempt alcohol abstinence for at least 30 days and reduce alcohol use afterwards
  • Willing to use smartphone applications and wrist biosensor devices for alcohol reduction; smartphone will be loaned if needed
  • Age between 35 and 70 years
Not Eligible

You will not qualify if you...

  • Psychiatric conditions interfering with study participation
  • Current alcohol withdrawal with CIWA score of 8 or higher or history of medically assisted detox
  • Two positive breath alcohol readings (> 0.00%) at in-person screening
  • Current or past 12 months inpatient or intensive addiction treatment
  • Psychosis or severe psychiatric disability
  • Pregnancy, nursing, or lack of reliable birth control in women not yet menopausal

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Outpatient Treatment

Duration - 60 days

Participants engage in behavioral interventions including counseling and use of a wrist biosensor and smartphone applications to support alcohol reduction.

Daily engagement during first 30 days, followed by weekly visits for the next 30 days

Follow-up

Duration - Up to 30 days after treatment

Participants are monitored for drinking reduction outcomes and non-drinking related health outcomes after treatment ends.

Periodic assessments up to 90 days from baseline

Trial Site Locations

Total: 2 locations

1

University of Miami

Coral Gables, Florida, United States, 33146

Actively Recruiting

2

University of Florida

Gainesville, Florida, United States, 32610

Actively Recruiting

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Research Team

E

Emmely Pavila

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

3

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