Assessing the efficacy and impact of a personalised smoking cessation intervention among type 2 diabetic smokers: study protocol for an open-label randomised controlled trial (DISCGO-RCT)

被引:4
作者
Clair, Carole [1 ,2 ]
Augsburger, Aurelie [1 ]
Birrer, Priska [1 ,2 ]
Locatelli, Isabella [1 ,2 ]
Schwarz, Joelle [1 ]
Greub, Gilbert [3 ]
Zanchi, Anne [4 ]
Jacot-Sadowski, Isabelle [5 ]
Puder, Jardena J. [6 ]
机构
[1] Ctr Primary Care & Publ Hlth, Dept Training Res & Innovat, Lausanne, Vaud, Switzerland
[2] Univ Lausanne, Fac Biol & Med, Lausanne, Switzerland
[3] Univ Hosp Lausanne, Ctr Res Intracellular Bacteria, Inst Microbiol, Lausanne, Switzerland
[4] Univ Hosp Lausanne, Serv Nephrol & Hypertens, Serv Endocrinol Diabet & Metab, Dept Med, Lausanne, Switzerland
[5] Ctr Primary Care & Publ Hlth, Dept Hlth Promot & Prevent, Lausanne, Vaud, Switzerland
[6] Univ Hosp Lausanne, Dept Woman Mother Child, Serv Obstet, Lausanne, Vaud, Switzerland
来源
BMJ OPEN | 2020年 / 10卷 / 11期
基金
瑞士国家科学基金会;
关键词
diabetes & endocrinology; general medicine (see internal medicine); preventive medicine; CORONARY-HEART-DISEASE; RISK-FACTORS; CIGARETTE-SMOKING; SELF-CARE; CARDIOVASCULAR MORTALITY; TRANSLATING RESEARCH; PHYSICAL-ACTIVITY; GLYCEMIC CONTROL; SEX DISPARITIES; MELLITUS;
D O I
10.1136/bmjopen-2020-040117
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionFew studies have assessed the efficacy of smoking cessation interventions in individuals with type 2 diabetes, but interventions adapted to the specific needs of this population are warranted. The aim of this study is to assess the efficacy of a smoking cessation intervention in a population of smokers with type 2 diabetes and to measure the metabolic impact of smoking cessation.Methods and analysisThe study is an open-label, randomised control trial. Participants recruited from a sanitary region of Switzerland will be randomly allocated to either the intervention or the control arm. The intervention group will have four individual counselling sessions over 12 weeks. Trained research nurses will conduct the behavioural intervention, using motivational interviews and addressing diabetes and gender specificities. The control group will have one short counselling session at baseline and will be given written information on smoking cessation. Both groups will have a follow-up visit at 26 and 52 weeks. Demographic and medical data will be collected at baseline and follow-up, along with blood and urine samples. The primary study outcome is continuous smoking abstinence validated by expired-air carbon monoxide from week 12 to week 52. Secondary study outcomes are continuous and 7-day point prevalence smoking abstinence at 12 and 26 weeks; change in motivation to quit and cigarette consumption; and change in glycosylated haemoglobin levels, body weight, waist circumference and renal function after smoking cessation. In a subsample of 80 participants, change in stool microbiota from baseline will be measured at 3, 8 and 26 weeks after smoking cessation.Ethics and disseminationEthical approval has been obtained by the competent ethics committee (Commission cantonale d'ethique de la recherche sur l'etre humain, CER-VD 2017-00812). The results of the study will be disseminated through publications in peer-reviewed journals and conference presentations.Trial registration numbersClinicalTrials.gov NCT03426423 and SNCTP000002762; Pre-results.
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页数:13
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