Postpartum Smoking Relapse Prevention by Breastfeeding Promotion
Primary Purpose
Smoking, Cigarette, Breastfeeding
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Breastfeeding promotion
Attention placebo control
Sponsored by
About this trial
This is an interventional prevention trial for Smoking, Cigarette focused on measuring Postpartum, Relapse
Eligibility Criteria
Inclusion Criteria:
- Be pregnant or in the first 1 month postpartum
- Be 18 years or older
- Have quit smoking cigarettes during or before this pregnancy
- Be willing to receive infant care and breastfeeding education
- Be able to read, listen, and talk in English
Exclusion Criteria:
- Medical conditions contraindicating breastfeeding such as HIV infection, active tuberculosis, and breast removal
- Current heavy drinking (more than 2 drinks a day)
- Current use of illicit substances
- Being strongly against breastfeeding
Sites / Locations
- Division of Behavioral Medicine Department of Pediatrics Jacobs School of Medicine and Biomedical Sciences State University of New York at BuffaloRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Breastfeeding intervention group
Attention placebo control group
Arm Description
A multicomponent behavioral intervention to promote breastfeeding
General infant care counseling and support
Outcomes
Primary Outcome Measures
Rates of smoking relapse
The date of postpartum relapse will be defined as the first day after delivery on which an ex-smoker has smoked for 7 consecutive days. Reported smoking abstinence will be verified by urine cotinine test.
Rates of smoking relapse
The date of postpartum relapse will be defined as the first day after delivery on which an ex-smoker has smoked for 7 consecutive days. Reported smoking abstinence will be verified by urine cotinine test.
Secondary Outcome Measures
Breastfeeding duration
Postpartum mothers will report their current feeding method, frequency, and duration of breastfeeding and/or formula use. Breastfeeding status will be visually verified by a female research staff, looking for one of the following indicators of successful breastfeeding in the infant - audible swallowing, a regular suck/swallow/breath pattern, or visible milk in the infant's mouth after they are not latched anymore.
Full Information
NCT ID
NCT04670822
First Posted
December 10, 2020
Last Updated
October 24, 2022
Sponsor
State University of New York at Buffalo
Collaborators
National Institutes of Health (NIH), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
1. Study Identification
Unique Protocol Identification Number
NCT04670822
Brief Title
Postpartum Smoking Relapse Prevention by Breastfeeding Promotion
Official Title
Postpartum Smoking Relapse Prevention by Breastfeeding Promotion
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
July 31, 2018 (Actual)
Primary Completion Date
July 31, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
State University of New York at Buffalo
Collaborators
National Institutes of Health (NIH), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
This is a randomized controlled trial to prevent postpartum smoking relapse by breastfeeding promotion. The intervention group (N=30) will receive multicomponent breastfeeding intervention from late pregnancy to 6 months postpartum, while the attention placebo control group (N=30) will receive general infant care counseling and support. The key outcome is the rate of postpartum smoking relapse.
Detailed Description
The investigators propose the first randomized controlled trial to reduce postpartum smoking relapse by breastfeeding promotion from late pregnancy to 6 months postpartum. The investigators will enroll 60 pregnant women who successfully quit smoking within 3 months before or during this pregnancy (<28 weeks). All participants will receive breastfeeding education during late pregnancy. Right after delivery, participants who are still smoking abstinent will be randomized into either the breastfeeding intervention group (N=30) or the attention placebo control group (N=30). The intervention group will receive multicomponent interventions consisting of postnatal lactation counseling, family/peer/employer support, contingent financial incentives, and early limited formula milk via syringe (optional for at-risk infants). The control group will receive counseling and support focusing on general infant care with attention and compensation similar to the intervention group. The primary outcomes are rates of postpartum smoking relapse verified by urine cotinine test.
Specific Aim 1 is to examine the efficacy of breastfeeding promotion intervention on postpartum smoking relapse. Specific Aim 2 is to collect preliminary data regarding potential mediating mechanisms: increases in lactation hormones (plasma oxytocin and prolactin), reductions in stress and negative affect, and enhancing mother-infant bonding and maternal motivation to protect the infant from secondhand smoke exposure. This innovative and feasible pilot study can yield promising preliminary data to strongly support our future application of a NIH R01 grant proposal that has the potential to reduce smoking-related harms to both the mother and the infant, and maximize the protective effects of breastfeeding on infant health and development.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Smoking, Cigarette, Breastfeeding
Keywords
Postpartum, Relapse
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Breastfeeding intervention group
Arm Type
Experimental
Arm Description
A multicomponent behavioral intervention to promote breastfeeding
Arm Title
Attention placebo control group
Arm Type
Placebo Comparator
Arm Description
General infant care counseling and support
Intervention Type
Behavioral
Intervention Name(s)
Breastfeeding promotion
Intervention Description
The intervention group will receive multicomponent interventions consisting of 7 half-hour postnatal visits for lactation counseling, family/peer/employer support, contingent financial incentives, and early limited formula milk via syringe (optional for at-risk infants).
Intervention Type
Behavioral
Intervention Name(s)
Attention placebo control
Intervention Description
The attention placebo control group will complete the same frequency and duration of study visits as the intervention group but focus on general infant care counseling and support.
Primary Outcome Measure Information:
Title
Rates of smoking relapse
Description
The date of postpartum relapse will be defined as the first day after delivery on which an ex-smoker has smoked for 7 consecutive days. Reported smoking abstinence will be verified by urine cotinine test.
Time Frame
6 months postpartum (post-test)
Title
Rates of smoking relapse
Description
The date of postpartum relapse will be defined as the first day after delivery on which an ex-smoker has smoked for 7 consecutive days. Reported smoking abstinence will be verified by urine cotinine test.
Time Frame
9 months postpartum (follow-up)
Secondary Outcome Measure Information:
Title
Breastfeeding duration
Description
Postpartum mothers will report their current feeding method, frequency, and duration of breastfeeding and/or formula use. Breastfeeding status will be visually verified by a female research staff, looking for one of the following indicators of successful breastfeeding in the infant - audible swallowing, a regular suck/swallow/breath pattern, or visible milk in the infant's mouth after they are not latched anymore.
Time Frame
Up to 9 months postpartum
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Be pregnant or in the first 1 month postpartum
Be 18 years or older
Have quit smoking cigarettes during or before this pregnancy
Be willing to receive infant care and breastfeeding education
Be able to read, listen, and talk in English
Exclusion Criteria:
Medical conditions contraindicating breastfeeding such as HIV infection, active tuberculosis, and breast removal
Current heavy drinking (more than 2 drinks a day)
Current use of illicit substances
Being strongly against breastfeeding
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xiaozhong Wen
Phone
17168296811
Email
xiaozhon@buffalo.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xiaozhong Wen
Organizational Affiliation
State University of New York at Buffalo
Official's Role
Principal Investigator
Facility Information:
Facility Name
Division of Behavioral Medicine Department of Pediatrics Jacobs School of Medicine and Biomedical Sciences State University of New York at Buffalo
City
Buffalo
State/Province
New York
ZIP/Postal Code
14214
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiaozhong Wen
Phone
716-829-6811
Email
xiaozhon@buffalo.edu
First Name & Middle Initial & Last Name & Degree
Xiaozhong Wen
Phone
7168296811
First Name & Middle Initial & Last Name & Degree
Xiaozhong Wen, MD, PhD
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Postpartum Smoking Relapse Prevention by Breastfeeding Promotion
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