Felix Naughton
Multicentre, randomised controlled trial of a low-cost smoking cessation text message intervention for pregnant smokers (MiQuit)
Naughton, Felix; Foster, Katharine; Emery, Jo; Cooper, Sue; Sutton, Stephen; Leonardi-Bee, Jo; Jones, Matthew; Ussher, Michael; Whitemore, Rachel; Leighton, Matthew; Montgomery, Alan; Parrott, Steve; Coleman, Tim
Authors
Katharine Foster
Jo Emery
Sue Cooper
Stephen Sutton
Professor JO LEONARDI-BEE JO.LEONARDI-BEE@NOTTINGHAM.AC.UK
PROFESSOR OF EVIDENCE SYNTHESIS
Dr MATTHEW JONES MATTHEW.JONES3@NOTTINGHAM.AC.UK
ASSISTANT PROFESSOR IN HEALTH ECONOMICS
Michael Ussher
Rachel Whitemore
Matthew Leighton
Professor ALAN MONTGOMERY ALAN.MONTGOMERY@NOTTINGHAM.AC.UK
DIRECTOR NOTTINGHAM CLINICAL TRIALS UNIT
Steve Parrott
Professor TIM COLEMAN tim.coleman@nottingham.ac.uk
PROFESSOR OF PRIMARY CARE
Abstract
Background: Text message cessation programmes have potential to change smoking behaviour during pregnancy but their effectiveness is unknown. This study aimed to estimate key parameters, including effectiveness and cost-effectiveness, for delivering a definitive effectiveness trial of a pregnancy specific, theory-guided, tailored text message cessation intervention.
Methods: Multicentre, single-blinded, randomised controlled trial. Pregnant smokers (<25 weeks gestation) were recruited from 16 antenatal screening clinics in England. Control participants received usual care and a smoking cessation leaflet. Intervention participants received the control components plus 12 weeks of individually-tailored, automated, interactive, cessation text messages (MiQuit). Key parameters to inform a full trial were recruitment and outcome ascertainment rates. 7 smoking outcomes were assessed; the planned primary outcome for the full trial was continuous abstinence from 4 weeks post-randomisation until 36 weeks gestation, validated biochemically. Estimated costs were modelled per quitter and per QALY.
Findings: 407 participants (203 MiQuit, 204 control) were randomised, 39% of those eligible. At follow-up, similar proportions per group provided self-report smoking status and a validation sample. More MiQuit participants achieved validated continuous abstinence relative to controls (5.4% vs. 2.0%; odds ratio [adjusted for site and gestation] 2.7, 95% CI 0.93 to 9.35). Adjusted odds ratios on other smoking outcomes ranged from 1.03 to 3.28 in favour of MiQuit. Incremental costs per quitter/QALY were £140.91 (95% CI -£192.87 to £617.96)/£3,623.09 (-£4,926.56 to £16,197.20), respectively, at the end of pregnancy.
Discussion: Findings imply that this low-cost text message intervention is likely to be effective and cost-effective. A full trial is warranted.
Citation
Naughton, F., Foster, K., Emery, J., Cooper, S., Sutton, S., Leonardi-Bee, J., Jones, M., Ussher, M., Whitemore, R., Leighton, M., Montgomery, A., Parrott, S., & Coleman, T. (2016, August). Multicentre, randomised controlled trial of a low-cost smoking cessation text message intervention for pregnant smokers (MiQuit). Presented at European Health Psychology Society and British Psychological Society Division of Health Psychology Conference 2016 (EHPS/DHP 2016)
Conference Name | European Health Psychology Society and British Psychological Society Division of Health Psychology Conference 2016 (EHPS/DHP 2016) |
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Start Date | Aug 23, 2016 |
End Date | Aug 27, 2016 |
Acceptance Date | May 1, 2016 |
Publication Date | Aug 23, 2016 |
Deposit Date | Aug 25, 2016 |
Publicly Available Date | Aug 25, 2016 |
Peer Reviewed | Peer Reviewed |
Public URL | https://nottingham-repository.worktribe.com/output/804600 |
Related Public URLs | http://www.ehps2016.org/ |
Contract Date | Aug 25, 2016 |
Files
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