Back to Search Start Over

TOB-STOP-COP (TOBacco STOP in COPd trial): study protocol—a randomized open-label, superiority, multicenter, two-arm intervention study of the effect of 'high-intensity' vs. 'low-intensity' smoking cessation intervention in active smokers with chronic obstructive pulmonary disease

Authors :
Mohamad Isam Saeed
Pradeesh Sivapalan
Josefin Eklöf
Charlotte Suppli Ulrik
Charlotta Pisinger
Therese Lapperre
Philip Tønnesen
Nils Hoyer
Julie Janner
Marie Lavesen Karlsson
Charlotte Sandau Bech
Kristoffer Marså
Nina Godtfredsen
Eva Brøndum
Birgit Munk
Merete Raaschou
Andrea Browatzski
Pernille Lütken
Jens-Ulrik Stæhr Jensen
Source :
Trials, Vol 21, Iss 1, Pp 1-10 (2020)
Publication Year :
2020
Publisher :
BMC, 2020.

Abstract

Abstract Background Cigarette smoking is the leading cause of chronic obstructive pulmonary disease (COPD), and it contributes to the development of many other serious diseases. Smoking cessation in COPD patients is known to improve survival and reduce the number of hospitalization-requiring acute exacerbations of COPD. However, smoking cessation interventions in these patients have only been successful for approximately 15–20% for consistent smoking abstinence in 12 months. Thus, more effective interventions are needed for this patient group. The aim of this study is to determine whether a high-intensity intervention compared to a low-intensity intervention can increase the proportion of persistent (> 12 months) anamnestic and biochemical smoking cessation in active smokers with COPD. Methods This study is a randomized controlled trial. A total of 600 active smokers with COPD will be randomly assigned 1:1 to either a standard treatment (guideline-based municipal smoking cessation program, “low intensity” group) or an intervention (“high-intensity” group) group, which consists of group sessions, telephone consultations, behavior design, hotline, and “buddy-matching” (smoker matched with COPD patient who has ceased smoking). Both groups will receive pharmacological smoking cessation. The primary endpoint is anamnestic and biochemical (cotinine analysis in urine) validated smoking cessation after 12 months. Discussion The potential benefit of this project is to improve smoking cessation rates and thereby reduce smoking-related exacerbations of COPD. In addition, the project can potentially benefit from increasing the quality of life and longevity of COPD patients and reducing the risk of other smoking-related diseases. Trial registration ClinicalTrials.gov NCT04088942 . Registered on 13 September 2019

Details

Language :
English
ISSN :
17456215
Volume :
21
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Trials
Publication Type :
Academic Journal
Accession number :
edsdoj.1a730c396d4b4aac8a6a9c182e8da253
Document Type :
article
Full Text :
https://doi.org/10.1186/s13063-020-04653-z