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ENHANCE-D:一项实用的三臂随机对照试验方案,比较强化戒烟干预措施与在牙科护理环境中为成年吸烟者提供的简短建议的效果。

ENHANCE-D: protocol for a pragmatic, 3-arm, randomised controlled trial comparing the impact of enhanced smoking cessation interventions to very brief advice for adult smokers in dental care settings.

作者信息

Holliday Richard, Wilson Nina, Ryan Vicky, Butcher Chrissie, Homer Tara, Watts Philippa, Kareithi Dorcas, Blaylock Paul, Ternent Laura, Finch Roland, Bissett Susan M, Todd Adam, Hancock Helen, Ellwood Fiona, Conway David I, Jakubovics Nicholas S, Kist Ralf, Holmes Richard D, Bauld Linda, Preshaw Philip M, McColl Elaine

机构信息

School of Dental Sciences, Faculty of Medical Sciences, Newcastle University, Newcastle Upon Tyne, UK.

Newcastle Upon Tyne Hospitals NHS Foundation Trust, Newcastle Upon Tyne, UK.

出版信息

Trials. 2025 Jul 28;26(1):261. doi: 10.1186/s13063-025-08954-z.

Abstract

BACKGROUND

Smoking is a key contributor to health inequalities, particularly impacting oral health. Periodontal (gum) health is significantly affected by smoking. With their extensive reach, regular and frequent patient contact, and potential teachable moments, dental teams are well placed to support patients to stop smoking. This is currently mainly provided through Very Brief Advice (VBA) interventions and so there is scope to enhance the cessation support offered. A large definitive trial is needed to confirm whether this would lead to improved smoking quit rates, improved oral health, and be good value for money.

METHODS

The ENHANCE-D trial is a multi-centre, pragmatic, definitive, 3-arm, parallel group, individually randomised controlled superiority trial, including an internal pilot, conducted in NHS dental settings. In total, 1215 patients who are current regular smokers will be randomly allocated using a 1:2:2 ratio to the following: (i) VBA; (ii) the offer of a standard course of Nicotine Replacement Therapy (NRT); (iii) or the offer of an e-cigarette starter kit. A subgroup of patients with periodontitis (gum disease) will have additional oral examinations and samples collected. The primary outcome is biochemically verified smoking abstinence at 6 months. A key secondary outcome is the percentage of periodontal sites with probing pocket depths (PPDs) ≥ 5 mm at 6 months in the periodontitis subgroup. Participants will be blinded to the purpose of the trial and not be aware of the treatment packages. Periodontal health outcomes will be recorded by trained and aligned assessors, blinded to intervention arm. Participant recruitment started in July 2022 with an internal pilot progressing to the main trial in May 2023. A qualitative process evaluation will explore participants' experiences of receiving the study interventions, alongside the views of dental teams, NHS commissioners, service managers, and policymakers. An economic evaluation will include a cost-effectiveness analysis and a cost-benefit analysis.

DISCUSSION

This will be the largest contemporary randomised trial of smoking cessation interventions in dental settings and one of the first to evaluate enhanced interventions. E-cigarettes were included as an intervention due to growing evidence of their effectiveness. They will be compared to VBA and NRT, and oral health outcomes assessed. The multi-centre, pragmatic design of this trial supports the external validity and potential for impacting clinical practice.

TRIAL REGISTRATION

ISRCTN 13158982. Registered on 10 May 2022. https://www.isrctn.com/ISRCTNISRCTN13158982.

摘要

背景

吸烟是导致健康不平等的关键因素,对口腔健康的影响尤为显著。牙周(牙龈)健康会受到吸烟的严重影响。牙科团队凭借其广泛的覆盖范围、与患者定期且频繁的接触以及潜在的可教育时机,非常适合支持患者戒烟。目前这主要通过极简短建议(VBA)干预来提供,因此有进一步加强戒烟支持的空间。需要开展一项大型确定性试验,以确认这是否会提高戒烟率、改善口腔健康并具有成本效益。

方法

ENHANCE - D试验是一项多中心、务实、确定性、三臂、平行组、个体随机对照优势试验,包括一项内部预试验,在英国国民健康服务(NHS)牙科机构中进行。总共1215名当前的经常吸烟者将按1:2:2的比例随机分配到以下组:(i)VBA;(ii)提供标准疗程的尼古丁替代疗法(NRT);(iii)或提供电子烟启动套件。患有牙周炎(牙龈疾病)的患者亚组将进行额外的口腔检查并采集样本。主要结局是6个月时经生化验证的戒烟情况。一个关键的次要结局是牙周炎亚组中6个月时探诊袋深度(PPD)≥5毫米的牙周部位百分比。参与者将对试验目的不知情,且不知道治疗方案。牙周健康结局将由经过培训且校准一致的评估人员记录,评估人员对干预组不知情。参与者招募于2022年7月开始,内部预试验于2023年5月进展到主要试验阶段。一项定性过程评估将探索参与者接受研究干预的体验,以及牙科团队、NHS专员、服务经理和政策制定者的观点。一项经济评估将包括成本效益分析和成本效益分析。

讨论

这将是牙科环境中当代最大规模的戒烟干预随机试验,也是首批评估强化干预措施的试验之一。由于电子烟有效性的证据越来越多,因此将其作为一种干预措施纳入。将其与VBA和NRT进行比较,并评估口腔健康结局。该试验的多中心、务实设计支持其外部有效性以及对临床实践产生影响的潜力。

试验注册

ISRCTN 13158982。于2022年5月10日注册。https://www.isrctn.com/ISRCTNISRCTN131589

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/52e2/12305899/e937de665886/13063_2025_8954_Fig1_HTML.jpg

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