Self-Monitoring of Carbon Monoxide to Enhance Reproductive Outcomes in Women

Not Applicable

Terminated

Brief Summary: Our goal is to study self-monitoring of smoking as a means to reduce smoking in pregnant women. Investigators hypothesize that more regular self-monitoring, text messages and feedback as provided by home carbon monoxide monitoring device combined with medical feedback on results will reduce smoking during pregnancy compared to only receiving text message and no self-monitoring by home monitoring device and no feedback by home carbon monoxide monitoring device . The periconceptual period is a life period, where given the immediacy of the fetus and future child, a pregnant woman is willing to try and modify potentially harmful behaviors.

Detailed Description: Altering unhealthy behaviors, such as tobacco smoking, that increase cardiovascular disease and cancer risk, has proven remarkably difficult in traditional medical practice settings, and successful medical trials have been costly and labor intensive. This proposal aims to utilize a self-monitoring device, i.e., carbon monoxide monitor to foster smoking cessation among pregnant women who smoke. Investigators hypothesize that women who have access to a self-monitoring device more frequently (i.e., at home) and receive feedback about their carbon monoxide level will have greater reductions in smoking as determined by declining serum cotinine levels over the course of the study compared to women who do not have access to a self-monitoring device and do not receive feedback about their carbon monoxide level, but only receive text messages.

Recruitment & Eligibility

Inclusion Criteria

Pregnant women 18-40 years old
Participants will be pregnant women estimated to be between 6 and 20 weeks into their pregnancy
Pregnant women have smoked at least at least one cigarette in the prior 7 days
Own a smartphone capable of delivering and receiving text messages

Exclusion Criteria

Project materials and text messages are in English, potential participants will be excluded if they cannot read English and if there are concerns about the ability to comprehend or comply with study procedures

Arm && Interventions

Group	Intervention	Description
CO monitor	piCO+ Smokerlyzer® monitor	Given a piCO+ Smokerlyzer® monitor, will receive daily text messages, will receive feedback about the relative level of carbon monoxide.
no CO monitor	Text messages	Not given a piCO+ Smokerlyzer® monitor, will receive daily text messages.
CO monitor	Text messages	Given a piCO+ Smokerlyzer® monitor, will receive daily text messages, will receive feedback about the relative level of carbon monoxide.

Primary Outcome Measures

Name	Time	Method
Primary Outcome of Serum Cotinine Levels	1 year	The primary outcome is the difference in serum cotinine levels between the intervention and control groups at the end of the trial.

Secondary Outcome Measures