Cytisine versus varenicline for smoking cessation for Māori (the indigenous people of New Zealand) and their extended family: protocol for a randomized non-inferiority trial

Addiction. 2019 Feb;114(2):344-352. doi: 10.1111/add.14449. Epub 2018 Nov 9.

Abstract

Background and aims: Cytisine, a nicotinic acetylcholine receptor partial agonist (like varenicline) found in some plants, is a low-cost, effective smoking cessation medication that may appeal to Māori [the indigenous people of New Zealand (NZ)]. The RAUORA trial aims to determine the effectiveness, safety and cost-effectiveness of cytisine (Tabex® ) versus varenicline (Champix® ) for smoking cessation in Māori and the whānau (extended family) of Māori.

Design: Pragmatic, community-based, open-label randomized non-inferiority trial.

Setting: Lakes District Health Board region, NZ.

Participants: Daily smokers (n = 2140) who self-identify as Māori or whānau of Māori, and are: aged ≥ 18 years, motivated to quit smoking in the next 2 weeks, eligible for subsidized varenicline, able to provide verbal consent and have daily access to a mobile phone/internet. Recruitment uses multi-media advertising.

Intervention and comparator: Participants are randomized (1 : 1 ratio) to receive a prescription for 12 weeks of cytisine tablets [following the manufacturer's dosing regimen for 25 days, then one 1.5-mg tablet every 6 hours (two per day) until 12 weeks] or varenicline tablets (following the manufacturer's dosing regimen). Both groups receive brief stop-smoking advice from the prescribing doctor and withdrawal-orientated behavioural support via community-based stop-smoking counselling services (frequency, duration and mode of delivery tailored for participants) or a research assistant (six weekly 10-15-minute calls). Participants are advised to reduce their smoking over the first 4 days of treatment, with day 5 as their designated quit-date.

Measurements: The primary outcome is carbon monoxide-verified continuous abstinence at 6 months post-quit date. Secondary outcomes at 1, 3, 6 and 12 months post-quit date include: self-reported continuous abstinence, 7-day point prevalence abstinence, cigarettes per day, time to (re)lapse, adverse events, treatment adherence/compliance, treatment acceptability, nicotine withdrawal/urge to smoke and health-care utilization/health-related quality of life.

Comments: This trial compares cytisine and varenicline when used by the indigenous people of NZ and their extended family for smoking cessation.

Keywords: Cytisine; effectiveness; indigenous; non-inferiority; randomized; safety trial; varenicline.

Publication types

  • Clinical Trial Protocol
  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alkaloids / therapeutic use*
  • Azocines / therapeutic use
  • Carbon Dioxide / analysis
  • Counseling
  • Equivalence Trials as Topic*
  • Family
  • Humans
  • Native Hawaiian or Other Pacific Islander / ethnology
  • New Zealand / ethnology
  • Patient Safety
  • Quinolizines / therapeutic use
  • Randomized Controlled Trials as Topic*
  • Smoking Cessation / methods*
  • Smoking Cessation Agents / therapeutic use*
  • Varenicline / therapeutic use*

Substances

  • Alkaloids
  • Azocines
  • Quinolizines
  • Smoking Cessation Agents
  • Carbon Dioxide
  • cytisine
  • Varenicline