Roelsgaard Ida Kristiane, Thomsen Thordis, Østergaard Mikkel, Christensen Robin, Hetland Merete Lund, Jacobsen Søren, Andersen Lena, Tønnesen Hanne, Rollefstad Silvia, Semb Anne Grete, Esbensen Bente Appel
Copenhagen Center for Arthritis Research (COPECARE), Center for Rheumatology and Spine Diseases, Rigshospitalet, Glostrup, Denmark.
Abdominal Centre, Rigshospitalet, Copenhagen, Denmark.
Trials. 2017 Nov 28;18(1):570. doi: 10.1186/s13063-017-2309-5.
Rheumatoid arthritis (RA) is a chronic, inflammatory rheumatic disease with the potential to induce significant disability. Patients with RA are at increased risk of cardiovascular diseases (CVD). Smokers with RA tend to experience more pain and fatigue, higher disease activity, more erosive joint destruction and a lower health-related quality of life (HR-QoL) than non-smokers. It remains to be determined whether these effects can be reduced by smoking cessation. This randomised controlled trial (RCT) in patients with RA aims to examine the effect of intensive smoking cessation intervention (motivational counselling combined with tailored nicotine replacement therapy) versus standard care on smoking cessation, and consequently on disease activity. Secondary objectives are to explore the effect on flare, risk factors for CVD, lung function, physical function, HR-QoL, pain and fatigue in patients with RA.
This will be a multicentre, open label, two arm, parallel group, RCT, including 150 daily smokers with RA, being in remission or having low-moderate disease activity (DAS28 ≤ 5.1). The intervention group (n = 75) will receive five counselling sessions with a trained smoking cessation counsellor based on the principles of motivational counselling. Furthermore, intervention patients will be offered nicotine replacement therapy tailored to individual needs. Participants randomised to the control group will receive standard care. The co-primary outcome is a hierarchical endpoint, which will be evaluated at 3 months follow-up and will include (1) self-reported smoking cessation biochemically validated by exhaled carbon monoxide and (2) achievement of EULAR clinical response (an improvement in DAS28 of > 0.6). Follow-up visits will be performed at 3, 6 and 12 months post-intervention.
This trial will reveal whether intensive smoking cessation counselling helps smokers with RA to achieve continuous smoking cessation and whether, as a concomitant benefit, it will reduce their RA disease activity. The trial aims to generate high quality evidence for the feasibility of a health promotion intervention for smokers with RA.
ClinicalTrials.gov, identifier: NCT02901886 . Registered on 10 September 2016. Recruitment status updated on 10th October 2016.
类风湿关节炎(RA)是一种慢性炎症性风湿性疾病,有可能导致严重残疾。类风湿关节炎患者患心血管疾病(CVD)的风险增加。与不吸烟者相比,患类风湿关节炎的吸烟者往往经历更多疼痛和疲劳、疾病活动度更高、关节侵蚀性破坏更严重且健康相关生活质量(HR-QoL)更低。这些影响是否可以通过戒烟来减轻仍有待确定。这项针对类风湿关节炎患者的随机对照试验(RCT)旨在研究强化戒烟干预(动机咨询结合量身定制的尼古丁替代疗法)与标准护理相比对戒烟的影响,进而对疾病活动度的影响。次要目标是探讨对类风湿关节炎患者病情复发、心血管疾病风险因素、肺功能、身体功能、健康相关生活质量、疼痛和疲劳的影响。
这将是一项多中心、开放标签、双臂、平行组随机对照试验,纳入150名患类风湿关节炎的每日吸烟者,病情处于缓解期或疾病活动度为低至中度(DAS28≤5.1)。干预组(n = 75)将接受由经过培训的戒烟顾问根据动机咨询原则进行的五次咨询。此外,干预组患者将获得根据个人需求量身定制的尼古丁替代疗法。随机分配到对照组的参与者将接受标准护理。共同主要结局是一个分层终点,将在3个月随访时进行评估,包括(1)通过呼出一氧化碳进行生化验证的自我报告戒烟情况,以及(2)达到欧洲抗风湿病联盟(EULAR)临床反应(DAS28改善>0.6)。干预后3、6和12个月将进行随访。
这项试验将揭示强化戒烟咨询是否有助于患类风湿关节炎的吸烟者实现持续戒烟,以及作为附带益处,它是否会降低他们的类风湿关节炎疾病活动度。该试验旨在为针对患类风湿关节炎的吸烟者的健康促进干预措施的可行性提供高质量证据。
ClinicalTrials.gov,标识符:NCT02901886。于2016年9月10日注册。2016年10月10日更新招募状态。