Skip to main content
Clinical Trials/NCT02412865
NCT02412865
Completed
Not Applicable

Developing and Scaling a Text Messaging Tool to Help Pregnant Smokers

George Washington University1 site in 1 country505 target enrollmentApril 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Smoking Cessation
Sponsor
George Washington University
Enrollment
505
Locations
1
Primary Endpoint
Knowledge as measured by survey items
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

The goal of this project is to evaluate the effectiveness (Phase II) of a text-based program to be called Quit4Baby to support smoking cessation efforts of pregnant women who smoke.

In Phase II, Dr. Abroms will conduct a randomized clinical trial among 500 pregnant smokers who have been recruited from users of text4baby - the first large scale mobile health application in the United States. Developed and operated by Voxiva and Healthy Mothers, Healthy Babies (HMHB)-collaborators in this program -text4baby is a free national service that has enrolled more than 800,000 pregnant women and mothers of infants 0-1 nationwide and delivered more than 150 million health messages to them including messages encouraging them not to smoke during pregnancy and referring them to quit lines.

Hypothesis 1: Pregnant smokers who receive quit4Baby + text4Baby will demonstrate higher levels of knowledge about the dangers of second hand smoke and the benefits of smoking cessation for mothers and their infants than text4baby only users.

Hypothesis 2: Pregnant smokers who receive quit4baby + text4baby will report significantly higher rates of calling a quit line, discussions with their health provider and/or use of cessation counseling than those who receive Text4baby alone.

Hypothesis 3: Pregnant smokers who receive quit4baby + text4baby will have significantly more favorable quitting outcomes compared with text4baby alone.

Registry
clinicaltrials.gov
Start Date
April 2015
End Date
February 2016
Last Updated
10 years ago
Study Type
Interventional
Study Design
Single Group
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Lorien Abroms

Associate Professor

George Washington University

Eligibility Criteria

Inclusion Criteria

  • Subscribe to the text4baby test messaging program
  • Smoke or recently quit (within last 2 weeks)- Smoking will be defined as self-report of smoking at least one cigarette in the past 7 days. Given that these individuals are recruited from text4baby users, we are confident that they will have cell phones and text messaging capacity.
  • Speak English
  • Willing to enroll in our study
  • 14 years old or older

Exclusion Criteria

  • No longer subscribe to text4baby
  • Not pregnant
  • Not current smoker (within past 2 weeks)
  • Non-English speakers
  • Not willing to receive Quit4Baby messages or enroll in study
  • Younger than 14 years of age

Outcomes

Primary Outcomes

Knowledge as measured by survey items

Time Frame: 1-6 months

Biometrically confirmed abstinence

Time Frame: 3-6 months

With saliva cotinine

Quitline call rates

Time Frame: 1-6 months

Study Sites (1)

Loading locations...

Similar Trials