Randomised controlled trial of tailored support to increase physical activity and reduce smoking in smokers not immediately ready to quit: protocol for the Trial of physical Activity-assisted Reduction of Smoking (TARS) Study
Rachael L Murray,
Paul Aveyard,
Helen Hancocks,
Jane Horrell,
Siobhan Creanor,
Michael Ussher,
Sarah Campbell,
Charlotte Wahlich,
Tess Harris,
Adrian Taylor,
Wendy Ingram,
Lisa Price,
Tom P Thompson,
Colin Green,
Adam Justin Streeter,
Jade Chynoweth,
Colin J Greaves,
Tristan Snowsill,
Lynne Callaghan,
Jennie King,
Alex Gude,
Mary George,
Louisa Hamilton,
Kelisha Cheema,
Dan Preece
Affiliations
Rachael L Murray
UK Centre for Tobacco Control Studies, Division of Epidemiology & Public Health, University of Nottingham, Nottingham, UK
Paul Aveyard
Nuffield Department of Primary Care Health Sciences, Oxford University, Oxford, UK
Helen Hancocks
3 Peninsula Clinical Trials Unit, University of Plymouth, Plymouth, UK
Jane Horrell
Community and Primary Care Research Group, University of Plymouth, Plymouth, UK
Siobhan Creanor
Centre for Health and Environmental Statistics, University of Plymouth, Plymouth, UK
Michael Ussher
2 Population Health Research Institute, St George’s University of London, London, UK
Sarah Campbell
4 Peninsula Clinical Trials Unit, University of Plymouth, Plymouth, UK
Charlotte Wahlich
1 Population Health Research Institute, St George`s, University of London, London, UK
Tess Harris
Population Health Research Institute, St Georges, University of London, London, UK
Adrian Taylor
4 Peninsula Medical School, Faculty of Health, University of Plymouth, Plymouth, UK
Wendy Ingram
School of Medicine, Faculty of Health, University of Plymouth, Plymouth, UK
Lisa Price
Sport and Health Sciences, University of Exeter, Exeter, UK
Tom P Thompson
School of Medicine, Faculty of Health, University of Plymouth, Plymouth, UK
Colin Green
College of Medicine and Health, University of Exeter, Exeter, UK
Adam Justin Streeter
School of Medicine, Faculty of Health, University of Plymouth, Plymouth, UK
Jade Chynoweth
Faculty of Health, University of Plymouth, Plymouth, UK
Colin J Greaves
School of Sport, Exercise & Rehabilitation Sciences, University of Birmingham, Birmingham, UK
Tristan Snowsill
College of Medicine and Health, University of Exeter, Exeter, UK
Lynne Callaghan
Faculty of Health, University of Plymouth, Plymouth, UK
Jennie King
School of Medicine, Faculty of Health, University of Plymouth, Plymouth, UK
Alex Gude
School of Medicine, Faculty of Health, University of Plymouth, Plymouth, UK
Mary George
Division of Population Health Sciences and Education, University of London, St George’s, London, UK
Louisa Hamilton
Nuffield Department of Primary Care Health Sciences, University of Oxford, Division of Public Health and Primary Health Care, Oxford, UK
Kelisha Cheema
School of Medicine, University of Nottingham, Nottingham, UK
Dan Preece
Public Health, Plymouth City Council, Windsor House, Plymouth, Devon, UK
Introduction Smoking reduction can lead to increased success in quitting. This study aims to determine if a client-focused motivational support package for smoking reduction (and quitting) and increasing (or otherwise using) physical activity (PA) can help smokers who do not wish to quit immediately to reduce the amount they smoke, and ultimately quit. This paper reports the study design and methods.Methods and analysis A pragmatic, multicentred, parallel, two group, randomised controlled superiority clinical trial, with embedded process evaluation and economics evaluation. Participants who wished to reduce smoking with no immediate plans to quit were randomised 1:1 to receive either (1) tailored individual health trainer face-to-face and/or telephone support to reduce smoking and increase PA as an aid to smoking reduction (intervention) or (2) brief written/electronic advice to reduce or quit smoking (control). Participants in both arms of the trial were also signposted to usual local support for smoking reduction and quitting. The primary outcome measure is 6-month carbon monoxide-confirmed floating prolonged abstinence following participant self-reported quitting on a mailed questionnaire at 3 and 9 months post-baseline. Participants confirmed as abstinent at 9 months will be followed up at 15 months.Ethics and dissemination Approved by SW Bristol National Health Service Research Committee (17/SW/0223). Dissemination will include publication of findings for the stated outcomes, parallel process evaluation and economic evaluation in peer-reviewed journals. Results will be disseminated to trial participants and healthcare providers.Trial registration number ISRCTN47776579; Pre-results.