跳至主要内容
临床试验/NCT02431611
NCT02431611已完成2 期

Biomarker Feedback to Motivate Tobacco Cessation in Pregnant Alaska Native Women (MAW) - Phase 3 Pilot Clinical Trial

Mayo Clinic2 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2015年3月最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
已完成
发起方
Mayo Clinic
入组人数
60
试验地点
2
主要终点
smoking abstinence in late pregnancy (self-reported abstinence verified with cotinine)

研究概览

简要总结

Phase 3 Pilot Clinical Trial.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • 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.

排除标准

  • 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.

研究组 & 干预措施

Control condition

Active Comparator

Control behavioral phone-based smoking cessation intervention

干预措施: Control condition (phone based smoking cessation counseling) (Behavioral)

Biomarker Feedback Intervention

Experimental

Biomarker feedback plus behavioral phone-based smoking cessation intervention

干预措施: Biomarker feedback (phone based smoking cessation counseling) (Behavioral)

结局指标

主要结局

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

时间窗: at week 36 gestation or greater up to the time of delivery

self-reported abstinence verified with cotinine

次要结局

  • Self-efficacy (Self-reported confidence scale)(at week 36 gestation or greater up to the time of delivery)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Christi Patten

PI

Mayo Clinic

研究点 (2)

Loading locations...

相似试验