CompletedNot applicableNCT05123118

Lung and Breast Cancer Prevention by an Integrated Intervention of Maternal Smoking Cessation and Breastfeeding

This pilot clinical trial aims to integrate maternal smoking cessation and breastfeeding interventions to enhance both cancer prevention behaviors. The investigators will recruit 40 daily smoking women in their early pregnancy and randomize them into the integrated intervention or control group. Main outcomes include smoking abstinence and breastfeeding rates at 6 months postpartum.

Checked against the public recordLast updated Apr 17, 2025 · Source: ClinicalTrials.gov

StatusCompleted
PhaseNot applicable
U.S. locations1
SponsorXiaozhong Wen
01
Study overview

What this study is about

Purpose
Prevention
Study type
Interventional
Phase
Not applicable
Sponsor
Xiaozhong Wen
Interventions being studied
Behavioral: Integrated intervention of smoking cessation and breastfeeding; Behavioral: Attention placebo control
02
Explore related studies

How this study is categorized

These labels come from structured fields and exact terms in the public record.

03
Public criteria

Who may be able to participate

Inclusion Criteria: * Be 18 years or older * At ≤28 weeks of pregnancy * Daily smoking cigarettes and/or cigars in the past 7 days * Be able to read, listen, and talk in English Exclusion Criteria: * Being diagnosed with cancer * Current heavy drinking (more than 2 drinks a day) * Current use of illicit substances * Medical conditions contraindicating breastfeeding such as HIV infection, active tuberculosis, and breast removal

Important: This is the sponsor’s public criteria, not a determination of eligibility. The study team must review your individual situation.

04
Study sites

U.S. locations

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

Source and freshness
Processed from ClinicalTrials.gov. Last public update: Apr 17, 2025. Always confirm current availability with the study team.

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