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Adapting an Intervention for Vaping in Young Veterans

Nicotine Cessation: Adapting a Counseling Program for Emerging Adults

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06196489
Enrollment
20
Registered
2024-01-09
Start date
2024-01-01
Completion date
2026-06-30
Last updated
2026-01-08

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

Conditions

E Cigarette Use

Keywords

Veteran, e-cigarette, vaping, young adult

Brief summary

The objective of this proposal is to adapt an evidence-based combustible tobacco counseling intervention following an evidence-based process to include e-cigarette use and update its components for emerging adults (EA). 1. Examine factors related to e-cigarette use, barriers to cessation, and facilitators of use of cessation services among an EA population. 2. Beta-test an initial version of the intervention, delivered via video telehealth and telephone, to examine usability and acceptability.

Detailed description

Use of electronic nicotine products (ENDS) has increased dramatically especially among young adults (EA- aged 18-30) and has been found to lead to immediate harmful health effects and increased addiction to combustible cigarette use. To date no research-tested interventions have been developed for helping people stop use of electronic nicotine products. Emerging adulthood is a developmental period that can lead to adoption of health risk behaviors. This proposal aims to address nicotine addiction by adapting an evidence-based counseling cessation intervention developed by the American Cancer Society (ACS) for a general population of combustible tobacco smokers, but found to be effective in EA. We will test two methods of providing counseling to participants: video telehealth or telephone. Primary outcome: Compared to self-help guide only, at 3 month follow-up, we hypothesize that participants in either counseling arm will have higher rates as compared to self-help only control of 7-day abstinence from using any nicotine product. This study fills a critical gap in ENDS research and will provide a model for further research into all-nicotine cessation in this vulnerable population.

Interventions

BEHAVIORALadapted vaping cessation intervention

Behavioral intervention for vaping cessation

Sponsors

University of California
CollaboratorOTHER
Veterans Medical Research Foundation
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
No

Inclusion criteria

* daily e-cigarette user for at least the past 6 months * 18-30 years old * willing to enroll in a program to quit nicotine use within 30 days * owns smartphone or computer/tablet with camera and internet connectivity * English speaker

Exclusion criteria

* ICD-10 diagnosis of dementia * current use of combustible tobacco products at least weekly

Design outcomes

Primary

MeasureTime frameDescription
e-cigarette use frequencyend of treatment (8 weeks post-baseline) and 30 days thereafternumber of days using e-cigarettes in the past 7 days at the time of assessment
e-cigarette use quantityend of treatment (8 weeks post-baseline) and 30 days thereafternumber of e-cigarette uses per day
Client Satisfaction Questionnaire (CSQ-8)end of treatment (8 weeks post-baseline) and 30 days thereafterParticipant satisfaction ratings; higher scores indicate greater satisfaction with the intervention

Countries

United States

Contacts

Primary ContactNeal M Doran, PhD
neal.doran@va.gov858-552-8585

Outcome results

None listed

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