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Attentional Bias Modification Training for E-cigarette Users

Attentional Bias Modification Training for E-cigarette Users

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05112562
Enrollment
50
Registered
2021-11-09
Start date
2021-06-09
Completion date
2024-12-31
Last updated
2022-11-04

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

Conditions

E-cigarette Use, Tobacco Use Cessation

Brief summary

Aims are to (1) evaluate attentional bias to e-cigarette cues between the intervention and control groups at post-intervention as compared to the pre-intervention; and (2) test the feasibility and efficacy of the intervention at post-intervention. To accomplish these aims, a theory-driven parallel, controlled 2-arm randomized clinical trial will be conducted with young adult e-cigarette users (approximately N = 50). Outcomes are attentional bias to e-cigarette cues and abstinence outcomes including nicotine dependence, and arousal/urges for e-cigarette use.

Interventions

BEHAVIORALComputerized attentional bias modification training

In intervention is designed to train participants to disengage attention from potent e-cigarette cues and is based on the well-established attention retraining paradigm for other psychopathologies.

BEHAVIORALPlacebo attention control training

This control training is very similar to the intervention's overall task structure and stimuli. The only difference is that the this control program is designed to exert no systematic manipulation on the attention deployment pattern between the two stimulus categories, thereby yielding no significant impact on the level of attentional bas toward ENDS-related cues

Sponsors

University of Wisconsin, Milwaukee
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 29 Years
Healthy volunteers
Yes

Inclusion criteria

* 18 and 29 years * Those who use ENDS exclusively, not combining with other tobacco, for 3 consecutive months * Those who own a smartphone.

Exclusion criteria

* Current medication or psychosocial treatment for ENDS dependence * Serious alcohol-use problems (≥ 26 points on the Alcohol Use Disorders Identification Test) * Ophthalmic conditions impeding eye-tracking * Current psychiatric/psychosocial treatment for other mental health disorders in the DSM-5 (e.g., schizophrenia) * Pregnancy.

Design outcomes

Primary

MeasureTime frameDescription
Attentional bias to e-cigarette cues measured by cueing taskPre-trainingAttentional bias measured by time in milliseconds between cue and response in cueing task

Secondary

MeasureTime frameDescription
Subjective urges for e-cigarette usePre-trainingSubjective urges for ENDS use measured by E-cigarette Use Patterns questionnaire)
Nicotine dependencePre-trainingNicotine dependence measured by Penn State E-Cigarette Dependence Index

Countries

United States

Contacts

Primary ContactSeok Hyun Gwon, PhD, RN
gwon@uwm.edu414-229-6462
Backup ContactHan Joo Lee, PhD
leehj@uwm.edu

Outcome results

None listed

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