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Clinical Trial 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.

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT05112562
Study type Interventional
Source University of Wisconsin, Milwaukee
Contact Seok Hyun Gwon, PhD, RN
Phone 414-229-6462
Email [email protected]
Status Recruiting
Phase N/A
Start date June 9, 2021
Completion date December 31, 2022

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