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Journal ArticleDOI

Outcome criteria in smoking cessation trials: proposal for a common standard

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TLDR
Six standard criteria comprising the 'Russell Standard' (RS) are proposed and it is believed that these criteria provide the best compromise between practicability and surrogacy for long-term cessation and will enable meaningful comparison between studies.
Abstract
Smoking cessation treatment is now integrated into many health-care systems and a major research effort is under way to improve current success rates. Until now results from randomized clinical trials have been reported in many different ways, leading to problems of interpretation. We propose six standard criteria comprising the 'Russell Standard' (RS). These criteria are applicable to trials of cessation aids where participants have a defined target quit date and there is face-to-face contact with researchers or clinic staff, as follows. (1) Follow-up for 6 months (RS6) or 12 months (RS12) from the target quit date or the end of a predefined 'grace period'; (2) self-report of smoking abstinence over the whole follow-up period allowing up to five cigarettes in total; (3) biochemical verification of abstinence at least at the 6-month or 12-month follow-up point; (4) use of an 'intention-to-treat' approach in which data from all randomized smokers are included in the analysis unless they have died or moved to an untraceable address (participants who are included in the analysis are counted as smokers if their smoking status at the final follow-up cannot be determined); (5) following-up 'protocol violators' and using their true smoking status in the analysis; and (6) collecting follow-up data blind to smokers' allocation to trial group. We believe that these criteria provide the best compromise between practicability and surrogacy for long-term cessation and will enable meaningful comparison between studies. There may be good reasons why other outcome criteria would also be reported, and studies that involve interventions with special groups or where there is no designated target quit date or face to face contact would need to adapt these criteria accordingly.

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Citations
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References
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Journal ArticleDOI

The Revised CONSORT Statement for Reporting Randomized Trials: Explanation and Elaboration

TL;DR: The Consort Statement as mentioned in this paper is a group of scientists and editors developed to improve the quality of reporting of randomized, controlled trials (RCTs) by providing guidance to authors about how to improve their reporting of their trials.
Journal ArticleDOI

A Comparison of Sustained-Release Bupropion and Placebo for Smoking Cessation

TL;DR: A double-blind, placebo-controlled trial of a sustained-release form of bupropion for smoking cessation, which excluded smokers with current depression, but not those with a history of major depression.
Journal ArticleDOI

Measures of abstinence in clinical trials: issues and recommendations.

TL;DR: A workgroup formed by the Society for Research on Nicotine and Tobacco reviewed the literature on abstinence measures used in trials of smoking cessation interventions and recommended that trials report multiple measures of abstinence.
Reference EntryDOI

Interventions for promoting smoking cessation during pregnancy

TL;DR: Smoking cessation interventions in pregnancy reduce the proportion of women who continue to smoke in late pregnancy, and reduce low birthweight and preterm birth.
Journal ArticleDOI

Effectiveness of interventions to help people stop smoking: findings from the Cochrane Library

TL;DR: This review aims to summarise evidence for the effectiveness of the available interventions and concludes that advice from doctors, structured interventions from nurses, and individual and group counselling are effective interventions.
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