Adapting an Intervention for Vaping in Young Veterans

Veterans Medical Research Foundation

Status: Enrolling

Conditions: E Cigarette Use

Treatments: Behavioral: adapted vaping cessation intervention

Study type: Interventional

Funder types: Other

Identifiers

NCT06196489

T31P1525 (Other Grant/Funding Number)

VeteransMRF

Details and patient eligibility

About

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.

Full 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.

Enrollment: 20 estimated patients

Sex: All

Ages: 18 to 30 years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

---

20 participants in 2 patient groups

telephone

Experimental group

Description:

Participants assigned to this group will receive the adapted intervention by telephone.

Treatment:

Behavioral: adapted vaping cessation intervention

Video

Experimental group

Description:

Participants assigned to this group will receive the adapted intervention by video telehealth.

Treatment:

Behavioral: adapted vaping cessation intervention