Disseminating and Implementing a Smoking Cessation Program for Pregnant and Postpartum Women
| Status: | Completed |
|---|---|
| Conditions: | Smoking Cessation, Smoking Cessation, Tobacco Consumers |
| Therapuetic Areas: | Pulmonary / Respiratory Diseases |
| Healthy: | No |
| Age Range: | 18 - 65 |
| Updated: | 10/14/2018 |
| Start Date: | November 2016 |
| End Date: | May 2018 |
Disseminating and Implementing a Smoking Cessation Program Fro Pregnant and Postpartum Women
This study tests whether a smoking cessation intervention for pregnant women that extends
postpartum (Striving to Quit (STQ)) can be implemented and disseminated outside of the
research environment that established its effectiveness (40% maintained biochemically
verified 6-month abstinence). The research aim is:
Is Striving to Quit more effective in achieving postpartum smoking cessation than "First
Breath," the current standard of care for pregnant women in Wisconsin who smoke?
250 women will be randomized into one of two study groups. Pregnant women in Group A (n=125)
will receive the existing First Breath prenatal intervention. Those in Group B (Striving to
Quit (STQ), n=125) will receive all Group A interventions, plus 1 additional prenatal home
visit, 3 postpartum in-home smoking cessation counseling visits, 3 postpartum phone calls,
and up to an additional $100 in gift cards. The primary outcome will be biochemically
confirmed smoking cessation at 6-months postpartum.
postpartum (Striving to Quit (STQ)) can be implemented and disseminated outside of the
research environment that established its effectiveness (40% maintained biochemically
verified 6-month abstinence). The research aim is:
Is Striving to Quit more effective in achieving postpartum smoking cessation than "First
Breath," the current standard of care for pregnant women in Wisconsin who smoke?
250 women will be randomized into one of two study groups. Pregnant women in Group A (n=125)
will receive the existing First Breath prenatal intervention. Those in Group B (Striving to
Quit (STQ), n=125) will receive all Group A interventions, plus 1 additional prenatal home
visit, 3 postpartum in-home smoking cessation counseling visits, 3 postpartum phone calls,
and up to an additional $100 in gift cards. The primary outcome will be biochemically
confirmed smoking cessation at 6-months postpartum.
Inclusion Criteria:
- Pregnant;
- enrolled in First Breath;
- Resides in Wisconsin counties of Calumet, Fond Du Lac, Kewaunee, Menominee, Oconto,
Shawno, Sheyboygan, Winnebago, Door, Brown, Outagamie, Manitowac, or Waupaca;
- English speaking;
- willingness to quit or reduce smoking in next 30 days or if already quit, desire to
remain quit after delivery;
- daily smoking (at least 1 cigarette/day for at least 1 week in past 6 months;
- willing to provide updates in contact information
Exclusion Criteria:
- not pregnant;
- not smoking in past 6 months;
- involved in another smoking research study.
We found this trial at
1
site
Madison, Wisconsin 53711
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