Wellness, Alcohol, Vitals, and Emotions
Recruiting now · Not applicable
Conditions studied: Alcohol Use
In brief
The goal of this clinical trial is to examine the effects of mindfulness based relapse prevention on self-regulation overtime and drinking in daily life through the use of wearable heart rate sensors during mindfulness groups and answering assessment questions 3 times per day during the course of treatment. The main questions that it aims to answer are: 1. What changes in self-regulation as measured through heart rate variability are observed during a mindfulness intervention and how do those self-regulatory changes affect drinking after treatment? 2. How do changes in heart rate variability affect drinking, craving, and negative affectivity in daily life? Participants will: 1. Answer questions related to their mood and drinking behaviors. 2. Wear their sensors during an 8-week treatment period with 1 group per week. 3. Answer questions 3 times a day during the treatment period. 4.) Return their sensors via a pre-stamped package and answer questions about their mood and drinking behaviors 3- and 6-months after the mindfulness groups end.
Key facts
- Study ID
- NCT06982443
- Run by
- University of New Mexico
- People needed
- 120
- Starts
- 2025-10-01
- Expected to finish
- 2029-09-01
- Last updated by the study team
- 2026-07-15
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 18 years of age or older
- Meet criteria for a moderate to severe alcohol use disorder within the previous 3-months.
- Able to attend group meetings at the time listed on the recruitment materials.
- Willing to wear a sensor for the 8-week intervention period and return the sensor after the immediate follow-up.
- Have a phone/tablet/computer with internet access.
- Be able to comprehend and consent to study requirements in English.
- Have access to a valid U.S. mailing address for receiving the HRV sensors and reside in the United States.
You may not qualify if…
- Current symptoms of psychosis or mania.
- Have a substance use disorder requiring a higher level of care than outpatient treatment (e.g., severe alcohol use disorder requiring inpatient detoxification).
- Have a history of pulmonary or cardiovascular disease that interferes with sensor data collection and HRV metrics (i.e., ectopic beats, arrythmia, congenital heart disease).
Where it is running
- University of New Mexico — Albuquerque, New Mexico, United States (enrolling)
Full record on ClinicalTrials.gov
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