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Adolescent Inpatient Tobacco and ENDS Intervention

Smoking Clinical Trial

Official title:
Development and Implementation of a Tobacco and ENDS Use Intervention for Adolescents and Young Adults in the Pediatric Hospital

Clinical Trial Summary

The purpose of this study is to develop and evaluate an evidence-based intervention to assist adolescents and young adults with current vaping to quit vaping and smoking.

Clinical Trial Description

Use of electronic nicotine delivery system (ENDS), which are noncombustible tobacco products (e.g., e-cigarettes), has increased dramatically among youth and is associated with numerous adverse health outcomes as well as use of alcohol and other illicit substances. National guidelines recommend counseling to address tobacco use at every adolescent clinical visit; however, many at-risk adolescents do not routinely attend primary care. Although evidence supports treatment of tobacco use during an adult hospitalization, no interventions have been developed or tested in the pediatric hospital setting. Based on promising theoretically-based evidence from the primary care and hospital settings, we will design, iteratively refine and assess implementation of a novel tobacco and ENDS use intervention for hospitalized adolescents and young adults (AYAs). We do so by conducting a randomized controlled pilot study (n=144) with 3-month follow up to evaluate preliminary efficacy as well as implementation outcomes (i.e., acceptability, feasibility, fidelity). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05936099
Study type Interventional
Source Children's Mercy Hospital Kansas City
Contact Abbey Masonbrink, MD, MPH
Phone 816-802-3236
Email armasonbrink@cmh.edu
Status Recruiting
Phase N/A
Start date August 1, 2023
Completion date July 10, 2025
View Details
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