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Clinical Trials/NCT03104452
NCT03104452
Completed
Not Applicable

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

University of Kansas Medical Center1 site in 1 country62 target enrollmentMarch 1, 2019

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Smoking Cessation
Sponsor
University of Kansas Medical Center
Enrollment
62
Locations
1
Primary Endpoint
Smoking status
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The purpose of this study is to learn how women's smoking changes during their pregnancy and as a new mom, and to assess the help they receive from their health care providers.

Detailed Description

Approximately 90% of women who smoked before pregnancy will be smokers within one year of delivery . This occurs even though half who smoke quit during the course of pregnancy. This is an observational, cohort study of pregnant women who smoked in the six months before becoming pregnant. Women will be followed from the first trimester to one year after the birth of their babies. The results of this study will help us to describe women's' views on the quality of tobacco counseling they receive from their doctors; understand patterns of smoking and quitting throughout pregnancy and after childbirth; and provide information needed to develop an intervention to help women quit.

Registry
clinicaltrials.gov
Start Date
March 1, 2019
End Date
July 31, 2021
Last Updated
4 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Smoked within six months prior to becoming pregnant or current smoking
  • Smoked at least 100 cigarettes
  • English speaking
  • Access to a cell phone
  • Willing to receive and send text messages.

Exclusion Criteria

  • Quit for longer than 6 months before becoming pregnant

Outcomes

Primary Outcomes

Smoking status

Time Frame: 1 year post-partum

The investigators will assess 7-day point prevalence smoking status over multiple time-points over the study period

Study Sites (1)

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