• Preventive medicine · Apr 2015

    Randomized Controlled Trial

    Efficacy of a tobacco quitline among adult cancer survivors.

    • Robert C Klesges, Rebecca A Krukowski, James L Klosky, Wei Liu, Deo Kumar Srivastava, James M Boyett, Jennifer Q Lanctot, Melissa M Hudson, Charla Folsom, Harry Lando, and Leslie L Robison.
    • Department of Epidemiology and Cancer Control, St. Jude Children's Research Hospital, Memphis, TN, USA; The Department of Preventive Medicine, University of Tennessee Health Science Center, Memphis, TN, USA. Electronic address: rklesges@uthsc.edu.
    • Prev Med. 2015 Apr 1; 73: 222722-7.

    ObjectiveThe purpose of the study (conducted 2010-2013) was to determine the efficacy of two common types of tobacco quitlines in adult cancer survivors who regularly smoked cigarettes.MethodAdult onset cancer survivors in Memphis, Tennessee (n=427, 67% female, 60% Caucasian) were randomized either to a Proactive (i.e., counselor-initiated calls) or Reactive (i.e., participant-initiated calls) quitline. Both conditions also received nicotine replacement therapy. The primary outcome was biochemically-verified (i.e., salivary cotinine) smoking cessation.ResultsWhile 12-month self-reported abstinence was consistent with other published studies of smoking cessation (22% and 26% point prevalence abstinence for Proactive and Reactive conditions, respectively), 48% of participants who were tested for cotinine failed biochemical verification, indicating a considerable falsification of self-reported cessation. Adjusted cessation rates were less than 5% in both intervention conditions.ConclusionOur results are consistent with other studies indicating that traditional smoking cessation interventions are ineffective among cancer survivors. Moreover, self-reports of cessation were unreliable in cancer survivors participating in a quitline intervention, indicating that future studies should include biochemical verification. Given the importance of smoking cessation among cancer survivors and low cessation rates in the current study, it may be necessary to design alternative interventions for this population. ClinicalTrials.gov identifier: NCT00827866.Copyright © 2015 Elsevier Inc. All rights reserved.

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