Accepted for/Published in: JMIR Research Protocols
Date Submitted: Jan 27, 2026
Open Peer Review Period: Jan 28, 2026 - Mar 2, 2026
Date Accepted: Mar 9, 2026
Date Submitted to PubMed: Mar 12, 2026
(closed for review but you can still tweet)
Telehealth-Delivered Mindfulness-Based Intervention: Protocol for a Randomized Clinical Trial for Individuals with Alcohol Use Disorder
ABSTRACT
Background:
Globally, approximately 8.6% of people will meet criteria for alcohol use disorder (AUD) in their lifetimes, with 2.2% meeting criteria for AUD in the past 12-months. In the United States, AUD prevalence is even greater with 13.9% meeting criteria in the past 12-months. Effective treatments for AUD exist, although most people receive help through mutual support groups (i.e., Alcoholics Anonymous (AA)). However, AA and other mutual support programs may not be desirable for all individuals, particularly those who do not seek abstinence-based approaches. Treatments that support reductions in drinking have been shown to be as effective as abstinence-based treatments in reducing alcohol-related harms and may be more appealing to a broader range of people. Mindfulness-based interventions may be particularly effective in supporting long-term recovery and whole person health and functioning for those with abstinent and non-abstinent recovery goals.
Objective:
This study is designed to test a novel rolling group-based mindfulness-based relapse prevention (MBRP) delivered via video conferencing, focused on drinking reduction goals and whole-person functioning.
Methods:
This study is a hybrid Type 1 effectiveness-implementation design to prospectively test the effectiveness of MBRP, and to identify barriers and facilitators of group participation to inform future implementation of MBRP as continuing care. Individuals with AUD (n=470) interested in stopping or reducing their drinking, meet criteria for AUD based on a symptom checklist, report heavy drinking at least once in the past 6 months, consent and understand study procedures in English, and provide a valid United States mailing address are recruited nationwide via online sources in the United States. Participants are randomized to either MBRP groups via Zoom or referral to online mutual support (e.g., AA). All participants receive an individual orientation session delivered via Zoom that includes brief motivational interviewing and an overview of their assigned condition and next steps (MBRP condition: overview of the MBRP groups and instructions on participating in MBRP via zoom; Referral condition: referral to online mutual support groups). Participants provide blood samples for phosphatidylethanol testing at baseline and 3-year follow-up and complete self-report measures of psychosocial functioning, alcohol and other drug use, addiction cycle domains, and previously established predictors of recovery every 6 months for 3 years.
Results:
Recruitment began on September 13, 2023 and the last recruited participant was randomized on March 20, 2025. Follow-up data collection is ongoing with all 6-month follow-ups completed (86.0% retention).
Conclusions:
This study evaluates the effectiveness and mechanisms of MBRP delivered via video conferencing, compared with referral to online mutual support groups, in supporting recovery among individuals with AUD. It also examines the reach, effectiveness, adoption, implementation, and maintenance of MBRP as an accessible, freely available continuing care option to support long-term recovery from AUD. Clinical Trial: This trial is registered on ClinicalTrials.gov under study record NCT06074341 with initial registration date of October 06, 2023.
Citation
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Copyright
© The authors. All rights reserved. This is a privileged document currently under peer-review/community review (or an accepted/rejected manuscript). Authors have provided JMIR Publications with an exclusive license to publish this preprint on it's website for review and ahead-of-print citation purposes only. While the final peer-reviewed paper may be licensed under a cc-by license on publication, at this stage authors and publisher expressively prohibit redistribution of this draft paper other than for review purposes.