Maternal Smoking Cessation and Pediatric Obesity Prevention

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age18-39
SponsorState University of New York at Buffalo

About this trial

The objective of this study is to test the effect of smoking cessation in pregnancy or in lactation on preventing rapid infant adiposity gain. Investigators propose a randomized, controlled experiment among smoking pregnant women from 1st prenatal care visit through 6 months of postpartum period. Two-phase randomization will be applied to separate the effects of smoking cessation in two different critical periods (i.e., pregnancy and lactation) on infant adiposity gain. Investigators will first randomly assign 40 smoking pregnant women into either the multicomponent intervention (N=30) or the education-only control group (N=10). The multicomponent intervention group will receive education and counseling, monitoring and feedback, contingent financial incentives, and family support, while the control group will receive education only. At the end of pregnancy, investigators will further randomize successful quitters (estimated N=20) from the multi-component intervention group into either the continuous multi-component intervention group in lactation (N=10) or the education-only control group (N=10). All women and their newborns will be followed from enrollment to 6 months postpartum. The key outcomes include maternal smoking abstinence confirmed by urine-cotinine and infant gain in weight-for-length z-score. Specific Aim 1 is to examine the effects of maternal smoking cessation intervention in pregnancy on infant gain in weight-for-length z-score from birth to 6 months. Specific Aim 2 is to examine the effect of maternal smoking abstinence intervention in lactation and infant post-weaning gain in weight-for-length z-score among the women who have successfully quit smoking in pregnancy.

Eligibility criteria

Qualifiers

Able to read, understand, and speak English.

Are 18-39 years old

Are less than 20 weeks of gestation

Have a singleton pregnancy

Disqualifiers

Previous history of major chronic disease or blood clotting disorders such as cancer, thyroid disorders, heart disease, kidney disease

Depression or have been diagnosed with depression or post-partum depression at any time

In treatment for Axis 1 disorders that prevent them following smoking cessation interventions

Trial design

Treatments tested in this trial

  • Multicomponent behavioral intervention
  • Education only control

Treatment groups

48 Participants
are divided into 2 treatment groups