Skip to content

Multi-Component Breath Alcohol Intervention

Development and Initial Testing of a Multi-Component Breath Alcohol- Focused Intervention for Young Adults

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06124898
Acronym
BAMTECH
Enrollment
24
Registered
2023-11-09
Start date
2023-11-09
Completion date
2024-08-29
Last updated
2026-05-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alcohol Drinking, Alcohol Use, Drinking Behavior

Brief summary

This is the first stage of a three-stage, NIH-funded study to develop and test initially a multi-modal intervention concerning blood/breath alcohol concentration for young adults. The multimodal intervention will be made up of brief telehealth counseling and psychoeducation and use of three mobile technologies to facilitate moderate drinking. In the first stage of the study, we will conduct formative research to obtain input from the study population, test initially the telehealth version of the brief counseling and psychoeducation and to develop a simple, "low tech" approach to coaching participants to use the three mobile technologies in typical drinking situations. Participation will last approximately one month.

Interventions

Participants will be asked to use the three mobile technologies as they choose while drinking for a two-week period.

Brief 25/30-minute motivational interview and psychoeducation on blood/breath alcohol concentration that includes both personalized and standardized information.

Study staff will review instructions for technology use closely with participants and guide them in use of existing phone technologies as reminders for use of the three moderate drinking technologies during drinking situations.

Sponsors

Northeastern University
Lead SponsorOTHER
National Institute on Alcohol Abuse and Alcoholism (NIAAA)
CollaboratorNIH

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 25 Years
Healthy volunteers
Yes

Inclusion criteria

* Be between the ages of 18-25 * Be able to read English and complete study evaluations * At least occasional heavy episodic drinking (i.e., 4 or more drinks for women and 5 or more drinks for men) over the prior 30 days * Frequent consumption of at least one alcoholic drink during a minimum of 12 days out of the prior 30 so that subjects will have multiple opportunities to use the moderate drinking technologies during the intervention period.

Exclusion criteria

* Severe substance use disorder * Be psychotic or otherwise severely psychiatrically disabled * Report a history of a medical condition that would contraindicate the consumption of alcohol (e.g., liver disease, cardiac abnormality, pancreatitis, diabetes, neurological problems, and gastrointestinal disorders)

Design outcomes

Primary

MeasureTime frameDescription
Technology utilizationAcross the field testing period, 2 weeksPercentage of reported drinking days on which one reports that moderate drinking technology use has occurred
AcceptabilityAt the end of the field testing period, 2 weeksScore on acceptability subscale of Modified System Usability Scale
UsabilityAt the end of the field testing period, 2 weeksScore on acceptability subscale of Modified System Usability Scale

Secondary

MeasureTime frameDescription
Drinks per drinking dayAcross the field testing period, 2 weeksNumber of drinks per day during field testing period
Estimated blood alcohol contentAcross the field testing period, 2 weeksAverage estimated blood alcohol content reached on drinking days
Negative consquencesAt the end of the field testing period, 2 weeksScore on the Young Adult Alcohol Consequences Questionnaire

Countries

United States

Contacts

PRINCIPAL_INVESTIGATORRobert F Leeman, PhD.

Northeastern University

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 15, 2026