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Improving Smoking Cessation in Socioeconomically-Disadvantaged Young Adults

University of Vermont logo

University of Vermont

Status

Completed

Conditions

Nicotine Dependence, Cigarettes

Treatments

Behavioral: Web + text smoking cessation intervention

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04379388
17-0351
P20GM103644 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The purpose of this study is to understand how to develop and deliver a better smoking cessation program for lower-income young adult smokers.

Full description

Using content and strategy developed from the formative research phase, this randomized smoking cessation trial will test the impact of a tailored cessation intervention for socioeconomically-disadvantaged young adult (SDYA) smokers compared to a usual-care control on intervention engagement, self-efficacy to quit, and 30-day point prevalence abstinence at 3-month follow-up.

This study will take place over a 3-month period. Individuals who complete the screening survey and are eligible to participate will be asked to complete a 15-20 minute baseline survey at the start of the study. This survey will ask questions about use of mobile phones, tobacco use, recent alcohol and other drug use, concerns about the coronavirus outbreak and how it may affect personal tobacco use, and physical activity. After the first survey, participants will be assigned randomly to one of two study groups:

Group A: Referral to a quit smoking hotline (quit line)

Group B: Referral to a quit smoking hotline (quit line), plus enrollment in a web and text-based smoking cessation intervention.

Participants in both groups will be enrolled after completing the following steps, in order:

  1. Providing consent to participate in the study;
  2. Confirming contact information;
  3. Completing a payment acknowledgement form that allows us to reimburse for survey/task completions; and
  4. Completing the baseline survey.

To complete enrollment, participants in Group B will also be required to register for an account on BecomeAnEx.org and enroll in text messages on the site. Once registered, Group B participants will be enrolled in a text message program customized for this study and will need to respond to the initial message from the text message platform to initiate text messages.

Participants in Group B will receive daily text messages for 3 months with content delivered through the Truth Initiative's BecomeAnEx digital quit smoking platform. They will also receive brief (1-2 minute) weekly check-in surveys related to the week's messages and smoking status during this time.

At 3-months, participants in both groups will receive the 15-minute follow-up assessment. Participants in both groups who report quitting smoking at 3-months will be mailed a kit in order to take a saliva test to measure the amount of cotinine, a metabolite of nicotine, in their saliva. Participants who report smoking at the 3-month follow-up will not receive this saliva test.

All study procedures will take place remotely, with surveys conducted online. Participants in Group A will be paid at least $30 for participation and up to $80. Participants in Group B will be paid at least $40 for participation and up to $170.

Enrollment

437 patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • age 18-30
  • lives in the U.S.
  • smoked at least 100 lifetime cigarettes
  • currently smokes every day or some days
  • interest in quitting smoking within the next 6 months
  • subjective financial situation of just meeting or not meeting basic expenses
  • access to a smartphone with internet

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

437 participants in 2 patient groups

Web + text smoking cessation intervention
Experimental group
Description:
Participants will receive referral to a quit smoking hotline and 12-week web and text-based smoking cessation intervention
Treatment:
Behavioral: Web + text smoking cessation intervention
Usual care control
No Intervention group
Description:
Participants will receive referral to a quit smoking hotline

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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