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Preoperative contingency management intervention for smoking abstinence in cancer patients: trial protocol for a multisite randomised controlled trial.
Rojewski, Alana M; Fucito, Lisa M; Baker, Nathaniel L; Palmer, Amanda M; Foster, Madeline G; Warren, Graham W; Bernstein, Steven L; Toll, Benjamin A.
Afiliación
  • Rojewski AM; Public Health Sciences, Medical University of South Carolina, Charleston, South Carolina, USA rojewski@musc.edu.
  • Fucito LM; Hollings Cancer Center, Charleston, South Carolina, USA.
  • Baker NL; Psychiatry, Yale School of Medicine, New Haven, Connecticut, USA.
  • Palmer AM; Public Health Sciences, Medical University of South Carolina, Charleston, South Carolina, USA.
  • Foster MG; Public Health Sciences, Medical University of South Carolina, Charleston, South Carolina, USA.
  • Warren GW; Pulmonary, Critical Care, Allergy, and Sleep Medicine, Medical University of South Carolina, Charleston, South Carolina, USA.
  • Bernstein SL; Public Health Sciences, Medical University of South Carolina, Charleston, South Carolina, USA.
  • Toll BA; Hollings Cancer Center, Charleston, South Carolina, USA.
BMJ Open ; 11(6): e051226, 2021 06 29.
Article en En | MEDLINE | ID: mdl-34187835
ABSTRACT

INTRODUCTION:

Continued smoking following a cancer diagnosis has substantial health risks including increased overall and cancer-specific mortality, risk of secondary malignancies, cancer treatment toxicity and risk of surgical complications. These risks can be mitigated by quitting smoking. The preoperative period represents a prime opportunity in which to administer robust smoking cessation treatment to both improve health and support and improve surgical outcomes. We will conduct a randomised clinical trial to evaluate the effectiveness of financial incentives delivered contingent on biochemically verified smoking abstinence (contingency management (CM)) in patients with cancer undergoing surgery. METHODS AND

ANALYSIS:

The study will take place across two study sites, and participants (N=282) who smoke, are diagnosed with or suspected to have any type of operable cancer and have a surgical procedure scheduled in the next 10 days to 5 weeks will be randomised to receive standard care plus Monitoring Only or CM prior to surgery. All patients will receive breath carbon monoxide (CO) tests three times per week, nicotine replacement therapy and counselling. The CM group will also earn payments for self-reported smoking abstinence confirmed by CO breath test ≤4 ppm on an escalating schedule of reinforcement (with a reset if they smoked). Point prevalence abstinence (PPA) outcomes (self-report of 7-day abstinence confirmed by CO≤4 ppm and/or anabasine ≤2 ng/mL) will be assessed on the day of surgery and 6 months after surgery. The effect of CM on 7-day PPA at the time of surgery and 6-month follow-up will be modelled using generalised linear mixed effects models. ETHICS AND DISSEMINATION This study has been reviewed and approved by the Medical University of South Carolina Institutional Review Board. We will disseminate our scientific results through traditional research-oriented outlets such as presentations at scientific meetings and publications in peer-reviewed journals. TRIAL REGISTRATION NUMBER NCT04605458.
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Texto completo: 1 Colección: 01-internacional Asunto principal: Cese del Hábito de Fumar / Neoplasias Tipo de estudio: Clinical_trials / Risk_factors_studies Límite: Humans Idioma: En Revista: BMJ Open Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Asunto principal: Cese del Hábito de Fumar / Neoplasias Tipo de estudio: Clinical_trials / Risk_factors_studies Límite: Humans Idioma: En Revista: BMJ Open Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos