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RECRUITING
NCT07661550
NA

Prevention of Postpartum Smoking Relapse and Related Health Consequences by Breastfeeding Promotion

Sponsor: State University of New York at Buffalo

View on ClinicalTrials.gov

Summary

The objective of this randomized controlled trial is to examine the efficacy of a new intervention to prevent postpartum smoking relapse and related health consequences through breastfeeding promotion. After the pre-test, ex-smokers who are still abstinent from smoking will be randomized into either the breastfeeding intervention or the attention placebo control group. The outcomes are postpartum smoking relapse, breastfeeding practices, and maternal and child health.

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

280

Start Date

2026-01-01

Completion Date

2031-07-31

Last Updated

2026-06-22

Healthy Volunteers

Yes

Interventions

BEHAVIORAL

Breastfeeding promotion

The intervention group will receive a multicomponent intervention promoting breastfeeding, including education, lactation counseling, social support, breastfeeding-contingent financial incentives, and early limited formula milk via syringe feeding (optional for at-risk infants).

BEHAVIORAL

Attention placebo control

The control group will receive instructions on general pregnancy and infant care from this project

Locations (1)

Division of Behavioral Medicine Department of Pediatrics Jacobs School of Medicine and Biomedical Sciences State University of New York at Buffalo

Buffalo, New York, United States