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Efficacy and Mechanisms of Mobile-Delivered Alcohol Attentional Bias Modification

Efficacy and Mechanisms of Mobile-Delivered Alcohol Attentional Bias Modification

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04263259
Enrollment
31
Registered
2020-02-10
Start date
2020-01-08
Completion date
2021-08-14
Last updated
2023-05-18

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

Conditions

Alcohol; Harmful Use

Brief summary

This study evaluates the efficacy as well as psychological and neurobiological mechanisms of mobile-delivered alcohol attentional bias modification among heavy drinking adults.

Detailed description

By testing the efficacy and neurobiological mechanisms of behavior change (MOBC) following attentional bias modification among heavy drinking adults, the proposed study has the potential to unify dual process models and neurobiological models of addiction. The cognitive retraining will be delivered via mobile electronic devices to ensure the cost-effectiveness of these procedures, to allow a large amount of retraining to be delivered in an ecologically valid manner, and to facilitate broad dissemination of such procedures if found to be efficacious. Using an intensive longitudinal experimental design, subjects will be randomly assigned into one of 2 groups (attentional bias modification vs. attentional bias control). Ecological momentary assessment (EMA) data will be used to assess changes in cognitive and behavioral measures in situ, and functional magnetic resonance imaging (fMRI) scans before and after cognitive retraining will be used to examine neural changes in specific regions of interest (ROI).

Interventions

Mobile-Delivered Cognitive Retraining Intervention

Sponsors

National Institute on Alcohol Abuse and Alcoholism (NIAAA)
CollaboratorNIH
University of New Mexico
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

Participants are not informed about the nature of the mobile-delivered intervention or their assignment to the intervention or control condition.

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* Alcohol Use Disorders Identification Test greater than or equal to 8 * right-handed

Exclusion criteria

* history of treatment for or diagnosis of alcohol use disorder/substance use disorder * history of brain injury * for females, currently pregnant * any MRI safety contraindication

Design outcomes

Primary

MeasureTime frameDescription
Alcohol Use Frequency4 weeksNumber of days of alcohol use during the 4-week ecological momentary assessment period
Alcohol Use Quantity4 weeksNumber of standard drinks per day during the 4-week ecological momentary assessment period
Negative Alcohol-Related Consequences4 weeksNumber negative consequences experienced 4-week ecological momentary assessment period

Secondary

MeasureTime frameDescription
Attentional Bias to Alcohol4 weeksMeasured with the Alcohol Dot Probe Task
Alcohol Cue-Induced Neural Reward Circuit Activation4 weeksRegions of interest include ventral tegmental area, dorsal and ventral striatum

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026