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Tobacco dependence treatment in the emergency department: A randomized trial using the Multiphase Optimization Strategy
被引:24
|作者:
Bernstein, Steven L.
[1
,2
,3
]
Dziura, James
[1
,2
]
Weiss, June
[1
]
Miller, Ted
[4
]
Vickerman, Katrina A.
[5
]
Grau, Lauretta E.
[2
]
Pantalon, Michael V.
[1
]
Abroms, Lorien
[6
]
Collins, Linda M.
[7
]
Toll, Benjamin
[8
]
机构:
[1] Yale Sch Med, Dept Emergency Med, 464 Congress Ave,Suite 260, New Haven, CT 06519 USA
[2] Yale Sch Publ Hlth, Dept Hlth Policy, New Haven, CT USA
[3] Yale Canc Ctr, New Haven, CT USA
[4] Pacific Inst Res & Evaluat, Calverton, MD USA
[5] Alere Wellbeing, Seattle, WA USA
[6] George Washington Univ, Milken Inst Sch Publ Hlth, Dept Prevent & Community Hlth, Washington, DC 20052 USA
[7] Penn State Univ, Methodol Ctr & Dept Human Dev & Family Studies, College Stn, TX USA
[8] Med Univ South Carolina, Dept Publ Hlth Sci, Charleston, SC 29425 USA
基金:
美国国家卫生研究院;
关键词:
Smoking cessation;
Tobacco dependence treatment;
Emergency department;
Mixed methods;
SMOKING-CESSATION;
MULTICOMPONENT INTERVENTION;
COST-EFFECTIVENESS;
POPULATION;
ABSTINENCE;
SERVICES;
SMOKERS;
POLICIES;
DESIGN;
LIFE;
D O I:
10.1016/j.cct.2017.12.016
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
Background: Tobacco dependence remains the leading preventable cause of death in the developed world. Smokers are disproportionately from lower socioeconomic groups, and may use the hospital emergency department (ED) as an important source of care. A recent clinical trial demonstrated the efficacy of a multi component intervention to help smokers quit, but the independent contributions of those components is unknown. Methods: This is a full-factorial (16-arm) randomized trial in a busy hospital ED of 4 tobacco dependence interventions: brief motivational interviewing, nicotine replacement therapy, referral to a telephone quitline, and a texting program. The trial utilizes the Multiphase Optimization Strategy (MOST) and a novel mixed methods analytic design to assess clinical efficacy, cost effectiveness, and qualitative participant feedback. The primary endpoint is tobacco abstinence at 3 months, verified by participants' exhaled carbon monoxide. Results: Study enrollment began in February 2017. As of April 2017, 52 of 1056 planned participants (4.9%) were enrolled. Telephone-based semi-structured participant interviews and in-person biochemical verification of smoking abstinence are completed at the 3-month follow-up. Efficacy and cost effectiveness analyses will be conducted after follow-up is completed. Discussion: The goal of this study is to identify a clinically efficacious, cost-effective intervention package for the initial treatment of tobacco dependence in ED patients. The efficacy of this combination can then be tested in a subsequent confirmatory trial. Our approach incorporates qualitative feedback from study participants in evaluating which intervention components will be tested in the future trial.
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页码:1 / 8
页数:8
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