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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

Authors :
Walker, N.
Smith, B.
Barnes, J.
Verbiest, M. E. A.
Kurdziel, T.
Parag, V.
Pokhrel, S.
Bullen, C.
Walker, N.
Smith, B.
Barnes, J.
Verbiest, M. E. A.
Kurdziel, T.
Parag, V.
Pokhrel, S.
Bullen, C.
Source :
Addiction vol.114 (2019) nr.2 p.344-352 [ISSN 0965-2140]
Publication Year :
2019

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

Details

Database :
OAIster
Journal :
Addiction vol.114 (2019) nr.2 p.344-352 [ISSN 0965-2140]
Notes :
DOI: 10.1111/add.14449, Addiction vol.114 (2019) nr.2 p.344-352 [ISSN 0965-2140], English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1124838242
Document Type :
Electronic Resource