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. 2021 Sep 14;2021(9):CD010216. doi: 10.1002/14651858.CD010216.pub6

ISRCTN61193406.

Study name Do e‐cigarettes help smokers quit when not accompanied by intensive behavioral support? A multi‐center randomized controlled trial
Methods RCT
Setting: UK
Multicenter. Participants will be recruited mainly from hospitals and GP practices across the UK by the Clinical Research Network. The study is being organized by Queen Mary University of London (QMUL)
Researchers from QMUL will provide the study treatment and conduct follow‐up calls
Participants 1170 people who smoke tobacco cigarettes
Inclusion criteria:
  • Adult daily smokers who are motivated to stop smoking

  • Must own a mobile phone and be willing to try either an online or texting treatment package, or both, or an e‐cigarette with or without telephone support.

  • Be happy to receive follow‐up calls

  • Be able to read/write/understand English


Exclusion criteria:
  • Women who are pregnant

  • Currently using an e‐cigarette

Interventions 1. Control: NHS Quit Now program (QN)
2. E‐cigarette starter pack with no ongoing support (EC)
3. EC starter pack with helpline support (EC+)
The study will aim to use a refillable EC that is similar to the type used in a previous EC trial (One Kit ‐ Innokin, UK Ecig Store), and one that is compliant with UK regulations, and not produced by a tobacco company
Outcomes Follow‐up at 4 weeks, 6 months and 12 months. CO at 6 and 12 months
Primary outcome measure:
Sustained smoking cessation at 6 months post‐TQD. This is measured by asking participants if they have smoked since their TQD at the 6‐month follow‐up. To be counted as a 'quitter', participants must report smoking no more than 5 cigarettes since 2 weeks post‐TQD with no smoking in the previous week, validated by carbon monoxide (CO) reading of < 8 ppm. Participants lost to follow‐up will be counted as smokers
Secondary outcome measures:
  • Validated sustained abstinence rates measured by asking smoking status and taking a carbon‐monoxide reading at 12 months post‐TQD

  • Validated sustained abstinence rates between 6 and 12 months, measured by asking smoking status and taking a carbon‐monoxide reading at 6 and 12 months

  • Self‐reported 7‐day point‐prevalence abstinence, measured by asking smoking status in last 7 days at 4 weeks, 6 months and 12 months post‐TQD

  • Cigarette consumption in non‐abstainers by vaping status, measured by questionnaire at four weeks, 6 and 12 months

  • Frequency and severity of urges to smoke and withdrawal symptoms, measured by questionnaire at 4 weeks post‐TQD.

  • Weight, measured by asking weight at 4 weeks, 6 months and 12 months post‐TQD

  • Respiratory symptoms, measured by questionnaire, at 4 weeks, 6 months and 12 months post‐TQD

  • Treatment adherence and ratings, measured by questionnaire at 4 weeks (and 6 and 12 months for EC arms)

  • Adverse reactions to EC, measured by questionnaire at 4 weeks, 6 and 12 months post‐TQD

  • Cost‐effectiveness of the interventions, measured by questionnaires at baseline, 6 and 12 months

  • Smokers' and health‐care professionals views and opinions of the helpline, measured by one‐off qualitative interviews separate to the main trial.

Starting date Overall trial start date: 01 September 2020
Trial end date: 31 May 2024
Not yet recruiting. Last edited 12 August 2020
Contact information Dr Katie Myers Smith, katie.smith@qmul.ac.uk
Notes