ClinicalTrials.Veeva

Menu

Establishing the Effectiveness of Publicly Available Smoking Cessation Resource

University of Virginia logo

University of Virginia

Status

Completed

Conditions

Smoking Cessation

Treatments

Behavioral: SmokefreeTXT

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this study is to evaluate the effectiveness of SmokefreeTXT, a smoking cessation text messaging program currently available to anyone in the United States through www.smokefree.gov, and to compare cessation outcomes for smokers living in different regions of Virginia while participants use the program. Participants will be asked to complete assessments at Baseline, 7 weeks, 3 months, and 6 months and will be asked to use a research version of SmokefreeTXT.

Enrollment

49 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age 18 and over
  • Current cigarette smoker (has smoked at least 100 cigarettes in their lifetime and currently smokes)
  • Ability to read and speak English
  • Resident of Virginia
  • Owns a cell phone

Exclusion criteria

  • Not a current smoker (e.g., started a quit attempt between providing interest information and starting the study)
  • Identity not able to be verified from information provided on interest form
  • Does not own a cell phone
  • Pregnant smoker or may become pregnant in the next 6 months
  • Lives in an area that has met recruitment criteria (after recruitment has begun)

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

49 participants in 1 patient group

SmokfreeTXT
Experimental group
Description:
Research version of the publicly available SmokefreeTXT program
Treatment:
Behavioral: SmokefreeTXT

Trial documents
1

Trial contacts and locations

1

Loading...

Central trial contact

Kara P. Wiseman

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems