RCT of a client-centred, caseworker-delivered smoking cessation intervention for a socially disadvantaged population

被引:15
作者
Bonevski, Billie [1 ]
Paul, Christine [2 ]
D'Este, Catherine [3 ]
Sanson-Fisher, Robert [2 ]
West, Robert [4 ]
Girgis, Afaf [1 ]
Siahpush, Mohammad [5 ]
Carter, Robert [6 ]
机构
[1] NSW Canc Council, Ctr Hlth Res & Psychooncol CHeRP, Newcastle, NSW, Australia
[2] Univ Newcastle, Sch Med & Publ Hlth, Discipline Hlth Behav, Newcastle, NSW 2308, Australia
[3] Univ Newcastle, Sch Med & Publ Hlth, CCEB, Newcastle, NSW 2308, Australia
[4] UCL, Dept Epidemiol & Publ Hlth, Canc Res UK Hlth Behav Res Ctr, London, England
[5] Univ Nebraska Med Ctr, Nebraska Med Ctr, Coll Publ Hlth, Dept Hlth Promot Social & Behav Hlth, Omaha, NE USA
[6] Deakin Univ, Burwood, Vic, Australia
基金
英国医学研究理事会;
关键词
NICOTINE REPLACEMENT THERAPY; PREVALENCE; STRATEGIES; SETTINGS; TOBACCO; TRIALS; WOMEN;
D O I
10.1186/1471-2458-11-70
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background: Disadvantaged groups are an important target for smoking cessation intervention. Smoking rates are markedly higher among severely socially disadvantaged groups such as indigenous people, the homeless, people with a mental illness or drug and alcohol addiction, and the unemployed than in the general population. This proposal aims to evaluate the efficacy of a client-centred, caseworker delivered cessation support intervention at increasing validated self reported smoking cessation rates in a socially disadvantaged population. Methods/Design: A block randomised controlled trial will be conducted. The setting will be a non-government organisation, Community Care Centre located in New South Wales, Australia which provides emergency relief and counselling services to predominantly government income assistance recipients. Eligible clients identified as smokers during a baseline touch screen computer survey will be recruited and randomised by a trained research assistant located in the waiting area. Allocation to intervention or control groups will be determined by time periods with clients randomised in one-week blocks. Intervention group clients will receive an intensive client-centred smoking cessation intervention offered by the caseworker over two face-to-face and two telephone contacts. There will be two primary outcome measures obtained at one, six, and 12 month follow-up: 1) 24-hour expired air CO validated self-reported smoking cessation and 2) 7-day self-reported smoking cessation. Continuous abstinence will also be measured at six and 12 months follow up. Discussion: This study will generate new knowledge in an area where the current information regarding the most effective smoking cessation approaches with disadvantaged groups is limited. Trial registration number: ISRCTN85202510
引用
收藏
页数:8
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