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Attentional Bias Modification Training for E-cigarette Users

U

University of Wisconsin, Milwaukee

Status

Enrolling

Conditions

Tobacco Use Cessation
E-cigarette Use

Treatments

Behavioral: Computerized attentional bias modification training
Behavioral: Placebo attention control training

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Enrollment

50 estimated patients

Sex

All

Ages

18 to 29 years old

Volunteers

Accepts Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

50 participants in 2 patient groups, including a placebo group

Computerized attentional bias modification training
Experimental group
Treatment:
Behavioral: Computerized attentional bias modification training
Placebo attention control training
Placebo Comparator group
Treatment:
Behavioral: Placebo attention control training

Trial contacts and locations

1

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Central trial contact

Han Joo Lee, PhD; Seok Hyun Gwon, PhD, RN

Data sourced from clinicaltrials.gov

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