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Alcohol Use DisorderNCT05747703

Telehealth Treatment for Alcohol Use Disorder

A study testing Ria Treatment Platform in people with Alcohol Use Disorder and Alcohol Dependence, run by Ria Health at 1 site in United States.

Active, not recruiting

Under way, not looking for participants. Everyone needed has enrolled. The study is still running.

Official record

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Trial summary

Participants with alcohol use disorder will be randomly assigned to either the Ria Treatment Platform or a waitlist control. The Ria Treatment Platform is a telehealth approach that incorporates medical assessment, medications for alcohol use disorder, individual and group coaching, educational video modules, and a… Read more about this study

Who is it for?
Ages 18 years and older
What is being tested?
Ria Treatment Platform
Could I receive a placebo?
No, everyone receives an active treatment
How many people
135 participants
Where
1 siteUnited States
Study dates
31 Jan 2024to Sep 2026
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • alcohol use disorder

Who cannot join

  • inability to provide informed consent

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Stanford University

    Stanford, California, 94305

Other trials in United States

About this study

Official title: A Telehealth Intervention to Increase Screening and Treatment for Alcohol Use Disorder

Participants with alcohol use disorder will be randomly assigned to either the Ria Treatment Platform or a waitlist control. The Ria Treatment Platform is a telehealth approach that incorporates medical assessment, medications for alcohol use disorder, individual and group coaching, educational video modules, and a Bluetooth-enabled breathalyzer. Patients are followed for three months during which data are collected, including measures of alcohol consumption and its consequences.

Being tested
Ria Treatment Platform
Medical subject headings
Alcoholism

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Ria Treatment PlatformCombination product

    combined medication, coaching, education, and monitoring

Study groups in NCT05747703
Study groupRoleWhat they receive
Ria Treatment PlatfromExperimentalThe Ria Treatment Platform is a telehealth approach that includes medical assessment, prescription of clinically appropriate medications for alcohol use disorder, individual and group coaching, educational video modules, and monitoring of breath alcohol concentrations through a Bluetooth-enabled breathalyzer.
Receives: Combination Product: Ria Treatment Platform
waitlist controlNo interventionPatients in this arm will not be provided treatment during the study period.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Percent of subjects without heavy drinking days

    Heavy drinking is defined as 5 or more standard drinks per day for men and 4 or more standard drinks per day for women, as assessed by the Timeline Followback.

    Measured: Final 4 weeks of the 12-week trial period

Secondary outcomes (2)
  1. Proportion of abstinent days

    Any drinking as assessed by the Timeline Followback

    Measured: 12-week trial period

  2. Liver function (ALT, AST, GGT)

    Measures of liver function.

    Measured: 12 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted28 Feb 2023
  2. Study start31 Jan 2024
  3. Primary completion21 Apr 2026
  4. Study completionSep 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Model description
participants will be randomly assigned in a 1:1 to the Ria Treatment Platform or a waitlist control condition
Masking
None (open label)
Enrolment
135 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT05747703
Sponsor's protocol ID
1A
Status last verified
Jun 2026
First submitted
17 Feb 2023
Last updated
30 Jun 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No

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