University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA
Corporal Michael J Crescenz VA Medical Center, Philadelphia, Pennsylvania, USA.
BMJ Open. 2024 Nov 18;14(11):e086698. doi: 10.1136/bmjopen-2024-086698.
Annual influenza vaccination reduces disease burden but vaccination rates are suboptimal, with persistent disparities among subpopulations. The purpose of this trial is to evaluate multicomponent behavioural economic nudge interventions to clinicians and patients to increase influenza vaccination. This trial also includes an intensification nudge to reduce disparities in vaccination among older adult, primary care patients.
This is a two-part, multisite cluster randomised, pragmatic clinical trial. In the first part, a multicomponent nudge intervention will be tested over approximately 6 months (September 2023-February 2024). The second part consists of a replication trial conducted at an additional site during the following influenza season (September 2024-February 2025). Primary care clinics will be randomised to the nudge intervention or usual care. Eligible clinicians and patients at intervention clinics will receive the intervention, and patients deemed high risk for not receiving a vaccine will be further randomised to receive an intensification nudge. The primary outcome is vaccine completion during the eligible visit and the secondary outcome is vaccine completion within 3 months of the eligible visit.
The effect of the clinic-level nudge intervention on the primary and secondary outcomes will be evaluated using generalised estimating equations (GEEs) with a clinic-level exchangeable working correlation to account for clustering of observations within the clinic. GEE models with an independent working correlation will be used to evaluate the impact of the additional intensification nudge on the primary and secondary outcomes.
The University of Pennsylvania Institutional Review Board (IRB) approved this trial and serves as the single IRB of record (IRB #851838). Results will be disseminated via peer-reviewed publication and conference presentations.
NCT06057727.
每年接种流感疫苗可减轻疾病负担,但疫苗接种率不理想,各亚人群之间仍存在持续差异。本试验旨在评估针对临床医生和患者的多组分行为经济学推动干预措施,以增加流感疫苗接种率。本试验还包括一项强化推动措施,以减少老年、初级保健患者中疫苗接种的差异。
这是一项两部分、多站点、集群随机、实用临床试验。在第一部分中,将在大约 6 个月(2023 年 9 月至 2024 年 2 月)内测试多组分推动干预措施。第二部分包括在随后的流感季节(2024 年 9 月至 2025 年 2 月)在另一个地点进行的复制试验。初级保健诊所将随机分配到推动干预组或常规护理组。干预诊所的合格临床医生和患者将接受干预措施,并且被认为有不接种疫苗风险的患者将进一步随机分配接受强化推动措施。主要结局是在合格就诊期间完成疫苗接种,次要结局是在合格就诊后 3 个月内完成疫苗接种。
使用广义估计方程(GEE)评估诊所层面推动干预对主要和次要结局的影响,GEE 模型采用诊所层面的可交换工作相关系数,以解释诊所内观察的聚类。将使用具有独立工作相关系数的 GEE 模型评估额外强化推动措施对主要和次要结局的影响。
宾夕法尼亚大学机构审查委员会(IRB)批准了这项试验,作为单一的 IRB 记录(IRB#851838)。结果将通过同行评审出版物和会议报告进行传播。
NCT06057727。