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A randomised controlled trial of a complex intervention to reduce children’s exposure to secondhand smoke in the home
  1. Elena Ratschen1,
  2. Rebecca Thorley2,3,
  3. Laura Jones4,
  4. Magdalena Opazo Breton2,3,
  5. Juliette Cook2,
  6. Ann McNeill3,5,
  7. John Britton2,3,6,
  8. Tim Coleman3,6,7,
  9. Sarah Lewis2,3
  1. 1 Department of Health Sciences, Mental Health and Addictions Research Group, University of York, York, UK
  2. 2 Department of Epidemiology and Public Health, University of Nottingham, Nottingham, UK
  3. 3 UK Centre for Tobacco and Alcohol Studies (UKCTAS), Nottingham, UK
  4. 4 Public Health, Epidemiology & Biostatistics, Institute of Applied Health Research, University of Birmingham, Birmingham, UK
  5. 5 National Addictions Centre, Institute of Psychiatry, King’s College London, London, UK
  6. 6 Nottingham University Hospital NHS Trusts, Nottingham, UK
  7. 7 Division of Primary Care, University of Nottingham, Nottingham, UK
  1. Correspondence to Dr Elena Ratschen, Department of Health Sciences, University of York, York, UK; elena.ratschen{at}york.ac.uk

Abstract

Objectives Exposing children to secondhand tobacco smoke (SHS) causes significant harm and occurs predominantly through smoking by caregivers in the family home. We report a trial of a complex intervention designed to reduce secondhand smoke exposure of children whose primary caregiver feels unable or unwilling to quit smoking.

Design An open-label, parallel, randomised controlled trial.

Setting Deprived communities in Nottingham City and County, England

Participants Caregivers resident in Nottingham City and County in England who were at least 18 years old, the main caregiver of a child aged under 5 years living in their household, and reported that they were smoking tobacco inside their home.

Interventions We compared a complex intervention combining personalised feedback on home air quality, behavioural support and nicotine replacement therapy for temporary abstinence with usual care.

Main outcomes The primary outcome was change in air quality in the home, measured as average 16–24  hours levels of particulate matter of  < 2.5  µm diameter (PM2.5), between baseline and 12 weeks. Secondary outcomes included changes in maximum PM2.5, proportion of time PM2.5 exceeded WHO recommended levels of maximum exposure of 25  µg/mg3, child salivary cotinine, caregivers’ cigarette consumption, nicotine dependence, determination to stop smoking, quit attempts and quitting altogether during the intervention.

Results Arithmetic mean PM2.5 decreased significantly more (by 35.2 %; 95%  CI 12.7% to 51.9 %) in intervention than in usual care households, as did the proportion of time PM2.5 exceeded 25  µg/mg3, child salivary cotinine concentrations, caregivers’ cigarette consumption in the home, nicotine dependence, determination to quit and likelihood of having made a quit attempt.

Conclusions By reducing exposure to SHS in the homes of children who live with smokers unable or unwilling to quit, this intervention offers huge potential to reduce children’s’ tobacco-related harm.

Trial registration number ISRCTN81701383.

This trial was funded by the UK National Institute for Health Research (NIHR): RP-PG-0608-10020

  • Secondhand smoke
  • Smoking Caused Disease
  • Addiction

This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/

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Footnotes

  • Contributors ER was chief investigator of the trial, responsible for strategic and staff management and led on the production of the paper; RT was the trial manager, responsible for the day-to-day management of the study and centrally involved in early stages of the write-up; LJ, SL, AMC, TC and JB designed a programme of work which led to development and evaluation of the intervention; LJ supported by SL, AMC and TC, developed and feasibility tested the intervention; LJ, SL, AMC and TC designed the randomised controlled trial; LJ set-up and managed the trial in its early stages; MOB was the trial statistician, supervised by SL who provided strategic and statistical senior support throughout the study; JC was involved as research assistants. All authors contributed to the continuous monitoring of trial progress, and to the production of the paper.

  • Competing interests None declared.

  • Ethics approval National Research Ethics Service West Midlands, Solihull.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Correction notice This article has been corrected since it was published Online First. The abstract stated that ’geometric' means were calculated. This was incorrect and has been changed to ’arithmetic'.

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