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Biomarker Feedback to Motivate Cessation in Pregnancy (MAW Phase 3)

Primary Purpose

Nicotine Dependence, Pregnancy

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Biomarker feedback (phone based smoking cessation counseling)
Control condition (phone based smoking cessation counseling)
Sponsored by
Mayo Clinic
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Nicotine Dependence

Eligibility Criteria

18 Years - 45 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Alaska Native
  • 18 years or older
  • provide written informed consent
  • be currently pregnant and at <24 weeks gestation
  • reside in Anchorage and plan to deliver at the ANMC
  • current tobacco user defined as any use of Iqmik, commercial ST, and/or cigarettes during the past 7 days.

Exclusion Criteria:

  • use of using nicotine replacement therapy or medications for tobacco cessation or participation in a behavioral cessation program within the past 30 days
  • another woman from the same household has enrolled.

Sites / Locations

  • Alaska Native Tribal Health Consortium

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Control condition

Biomarker Feedback Intervention

Arm Description

Control behavioral phone-based smoking cessation intervention

Biomarker feedback plus behavioral phone-based smoking cessation intervention

Outcomes

Primary Outcome Measures

smoking abstinence in late pregnancy (self-reported abstinence verified with cotinine)
self-reported abstinence verified with cotinine

Secondary Outcome Measures

Self-efficacy (Self-reported confidence scale)
Self-reported confidence scale

Full Information

First Posted
April 14, 2015
Last Updated
December 15, 2017
Sponsor
Mayo Clinic
Collaborators
Alaska Native Tribal Health Consortium, University of California, San Francisco, University of Minnesota
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1. Study Identification

Unique Protocol Identification Number
NCT02431611
Brief Title
Biomarker Feedback to Motivate Cessation in Pregnancy
Acronym
MAW Phase 3
Official Title
Biomarker Feedback to Motivate Tobacco Cessation in Pregnant Alaska Native Women (MAW) - Phase 3 Pilot Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2017
Overall Recruitment Status
Completed
Study Start Date
March 2015 (undefined)
Primary Completion Date
December 2017 (Actual)
Study Completion Date
December 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mayo Clinic
Collaborators
Alaska Native Tribal Health Consortium, University of California, San Francisco, University of Minnesota

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Phase 3 Pilot Clinical Trial.
Detailed Description
Developing effective tobacco cessation interventions during pregnancy for American Indian and Alaska Native people is a national priority and will contribute to the U.S. public health objective of reducing tobacco-related cancer health disparities. The proposed project builds on the investigators' successful partnership with the Alaska Native community and previous work with Alaska Native pregnant women. The investigators propose to develop and test a novel biomarker feedback intervention relating cotinine levels in the urine of pregnant women with the woman and infant's likely exposure to the tobacco specific nitrosamine and carcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone) (NNK). This 5-year project will be conducted in three phases. In Phase 1 the investigators will utilize a non-randomized, clinical observational trial to examine biomarkers of nicotine and carcinogen exposure (urine cotinine and total NNAL [a metabolite of NNK], respectively) among 150 maternal-infant pairs with assessments conducted during pregnancy and at delivery. In Phase 2, the investigators will obtain qualitative feedback on the findings from Phase 1 through individual interviews conducted with 32 women who use tobacco to develop the biomarker feedback intervention messages. Phase 3 will consist of a formative evaluation of the biomarker feedback intervention with 60 pregnant women using a two-group randomized design to assess the intervention's feasibility and acceptability, and the biochemically confirmed abstinence rate at the end of pregnancy. All phases of the project will be guided by a Community Advisory Committee. Each phase is an important step to advance the investigators' understanding of the potential for biomarker feedback as a strategy to help Alaska Native pregnant women quit tobacco use. The potential reach of the intervention is significant from a public health perspective as over 600 tobacco users deliver each year at the Alaska Native Medical Center in Anchorage where the proposed project will take place. Developing effective interventions for tobacco cessation during pregnancy is important to reduce adverse health consequences for the mother and neonate and future risk of tobacco-caused cancers. This is the third and final phase of the project.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Nicotine Dependence, Pregnancy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control condition
Arm Type
Active Comparator
Arm Description
Control behavioral phone-based smoking cessation intervention
Arm Title
Biomarker Feedback Intervention
Arm Type
Experimental
Arm Description
Biomarker feedback plus behavioral phone-based smoking cessation intervention
Intervention Type
Behavioral
Intervention Name(s)
Biomarker feedback (phone based smoking cessation counseling)
Intervention Description
Feedback on maternal cotinine and likely infant NNAL Phone based behavioral smoking cessation counseling
Intervention Type
Behavioral
Intervention Name(s)
Control condition (phone based smoking cessation counseling)
Intervention Description
phone-based behavioral smoking cessation counseling
Primary Outcome Measure Information:
Title
smoking abstinence in late pregnancy (self-reported abstinence verified with cotinine)
Description
self-reported abstinence verified with cotinine
Time Frame
at week 36 gestation or greater up to the time of delivery
Secondary Outcome Measure Information:
Title
Self-efficacy (Self-reported confidence scale)
Description
Self-reported confidence scale
Time Frame
at week 36 gestation or greater up to the time of delivery

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Alaska Native 18 years or older provide written informed consent be currently pregnant and at <24 weeks gestation reside in Anchorage and plan to deliver at the ANMC current tobacco user defined as any use of Iqmik, commercial ST, and/or cigarettes during the past 7 days. Exclusion Criteria: use of using nicotine replacement therapy or medications for tobacco cessation or participation in a behavioral cessation program within the past 30 days another woman from the same household has enrolled.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christi A Patten, PhD
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Alaska Native Tribal Health Consortium
City
Anchorage
State/Province
Alaska
ZIP/Postal Code
99577
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

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Biomarker Feedback to Motivate Cessation in Pregnancy

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