Protocol for the Smoking, Nicotine and Pregnancy (SNAP) trial:: double-blind, placebo-randomised, controlled trial of nicotine replacement therapy in pregnancy

被引:34
|
作者
Coleman, Tim [1 ]
Thornton, Jim
Britton, John
Lewis, Sarah
Watts, Kim
Coughtrie, Michael W. H.
Mannion, Clare
Marlow, Neil
Godfrey, Christine
机构
[1] Univ Nottingham, Div Primary Care, Nottingham NG7 2RD, England
[2] Univ Nottingham, Div Obstet & Gynecol, Nottingham NG7 2RD, England
[3] Univ Nottingham, Div Resp Med, Nottingham NG7 2RD, England
[4] Univ Nottingham, Acad Div Midwifery, Nottingham NG7 2RD, England
[5] Univ Dundee, Dept Mol & Cellular Pathol, Dundee, Scotland
[6] Cent Cheshire PCT, Stop Smoking Serv, Crewe, England
[7] Univ Nottingham, Acad Div Child Hlth, Nottingham NG7 2RD, England
[8] Univ York, Dept Hlth Sci, York YO10 5DD, N Yorkshire, England
关键词
D O I
10.1186/1472-6963-7-2
中图分类号
R19 [保健组织与事业(卫生事业管理)];
学科分类号
摘要
Background: Smoking in pregnancy remains a public health challenge. Nicotine replacement therapy (NRT) is effective for smoking cessation in non-pregnant people, but because women metabolise nicotine and cotinine much faster in pregnancy, it is unclear whether this will be effective for smoking cessation in pregnancy. The NHS Health Technology Assessment Programme (HTA)-funded smoking, nicotine and pregnancy ( SNAP) trial will investigate whether or not nicotine replacement therapy ( NRT) is effective, cost-effective and safe when used for smoking cessation by pregnant women. Methods/Design: Over two years, in 5 trial centres, 1050 pregnant women who are between 12 and 24 weeks pregnant will be randomised as they attend hospital for ante-natal ultrasound scans. Women will receive either nicotine or placebo transdermal patches with behavioural support. The primary outcome measure is biochemically-validated, self-reported, prolonged and total abstinence from smoking between a quit date ( defined before randomisation and set within two weeks of this) and delivery. At six months after childbirth self-reported maternal smoking status will be ascertained and two years after childbirth, self-reported maternal smoking status and the behaviour, cognitive development and respiratory symptoms of children born in the trial will be compared in both groups. Discussion: This trial is designed to ascertain whether or not standard doses of NRT ( as transdermal patches) are effective and safe when used for smoking cessation during pregnancy.
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