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Clinical Trials/NCT05041413
NCT05041413
Completed
Not Applicable

Enhancing the Delivery of Tobacco Treatment During Pregnancy and Postpartum Though Systems-Change

University of Kansas Medical Center1 site in 1 country30 target enrollmentAugust 11, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Smoking Cessation
Sponsor
University of Kansas Medical Center
Enrollment
30
Locations
1
Primary Endpoint
Days abstinent in the past 30 days
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

The objective of this study is to test the feasibility and preliminary effectiveness of a tailored text message program to support smoking abstinence among postpartum women who smoke or recently quit.

Detailed Description

This pilot trial will evaluate a text message intervention (Moms Quit) to be initiated with postpartum women within one month of delivery. Moms Quit is a tailored program to support smoking abstinence among new mothers who are either current smokers or quit during their most recent pregnancy. Investigators will randomize 30 postpartum women, stratified by recent/current smoking status, into Moms Quit versus vs. CONTROL. Investigators hypothesize that participants receiving Moms Quit will have, on average, a significantly longer period of self-reported prolonged abstinence compared to CONTROL.

Registry
clinicaltrials.gov
Start Date
August 11, 2021
End Date
October 5, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Less than one month postpartum
  • Live delivery
  • Smoked at least 100 cigarettes/lifetime
  • Smoked anytime during their most recent pregnancy
  • English-speaking
  • Own a mobile phone
  • Provide an email address
  • Willing to receive intervention-related texts
  • Willing to complete surveys
  • Willing to provide a saliva sample at the end of the study

Exclusion Criteria

  • Women whose pregnancy did not result in live birth
  • On a 7-point scale, participant indicates that they are not interested in quitting or staying quit in the next 6 months (Not at all = 1).

Outcomes

Primary Outcomes

Days abstinent in the past 30 days

Time Frame: 12 weeks post-randomization

Self-reported abstinence in the past 30 days

Secondary Outcomes

  • 7 day point prevalence abstinence(12 weeks post-randomization)

Study Sites (1)

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