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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
- Source :
- Trials, Vol 21, Iss 1, Pp 1-10 (2020), Trials, Saeed, M I, Sivapalan, P, Eklöf, J, Ulrik, C S, Pisinger, C, Lapperre, T, Tønnesen, P, Hoyer, N, Janner, J, Karlsson, M L, Bech, C S, Marså, K, Godtfredsen, N, Brøndum, E, Munk, B, Raaschou, M, Browatzski, A, Lütken, P & Jensen, J-U S 2020, ' 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 ', Trials, vol. 21, 730 . https://doi.org/10.1186/s13063-020-04653-z
- Publication Year :
- 2020
- Publisher :
- BMC, 2020.
-
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
- Subjects :
- medicine.medical_specialty
medicine.medical_treatment
Medicine (miscellaneous)
Equivalence Trials as Topic
Smoking cessation
law.invention
Exacerbations
03 medical and health sciences
chemistry.chemical_compound
Pulmonary Disease, Chronic Obstructive
Study Protocol
0302 clinical medicine
Randomized controlled trial
law
Internal medicine
medicine
Clinical endpoint
Humans
Multicenter Studies as Topic
COPD
Pharmacology (medical)
030212 general & internal medicine
Varenicline
lcsh:R5-920
Smokers
business.industry
Standard treatment
Guideline
medicine.disease
Tobacco Use Cessation Devices
Treatment Outcome
chemistry
Quality of Life
Human medicine
Cotinine
business
lcsh:Medicine (General)
030217 neurology & neurosurgery
Subjects
Details
- Language :
- English
- ISSN :
- 17456215
- Volume :
- 21
- Issue :
- 1
- Database :
- OpenAIRE
- Journal :
- Trials
- Accession number :
- edsair.doi.dedup.....bc0c8700b772125ffcfdd1c0ca9a319b
- Full Text :
- https://doi.org/10.1186/s13063-020-04653-z