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Quit4Baby Evaluation

Developing and Scaling a Text Messaging Tool to Help Pregnant Smokers

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02412865
Acronym
Quit4Baby
Enrollment
505
Registered
2015-04-09
Start date
2015-04-30
Completion date
Unknown
Last updated
2016-02-26

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

Conditions

Pregnancy, Smoking Cessation

Keywords

mhealth

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.

Interventions

BEHAVIORALQuit4Baby
BEHAVIORALText4Baby

Sponsors

George Washington University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
14 Years to 44 Years
Healthy volunteers
Yes

Inclusion criteria

1. Subscribe to the text4baby test messaging program 2. Pregnant 3. 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. 4. Speak English 5. Willing to enroll in our study 6. 14 years old or older

Exclusion criteria

1. No longer subscribe to text4baby 2. Not pregnant 3. Not current smoker (within past 2 weeks) 4. Non-English speakers 5. Not willing to receive Quit4Baby messages or enroll in study 6. Younger than 14 years of age

Design outcomes

Primary

MeasureTime frameDescription
Biometrically confirmed abstinence3-6 monthsWith saliva cotinine
Quitline call rates1-6 months
Knowledge as measured by survey items1-6 months

Countries

United States

Outcome results

None listed

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