Magnan Elizabeth, Gosdin Melissa, Tancredi Daniel, Jerant Anthony
Department of Family and Community Medicine, University of California Davis, Sacramento, CA, USA.
Center for Healthcare Policy and Research, University of California Davis, Sacramento, CA, USA.
J Multimorb Comorb. 2021 Dec 1;11:26335565211062387. doi: 10.1177/26335565211062387. eCollection 2021 Jan-Dec.
Multimorbidity is common, and care is impacted by patient life context. Effective, efficient interventions to improve patient-centered outcomes such as perceived treatment burden are limited. There is a need for interventions that integrate patient contextual information into primary care encounters to improve such outcomes. Patient life context is a multitude of factors that influence a patient's life and healthcare, including social determinants of health and broader elements such as family and work demands.
This pilot randomized controlled trial (RCT) protocol will compare standard pre-visit planning to pre-visit planning that incorporates the patient's life context, for patients with diabetes plus other chronic comorbid conditions. Primary outcomes include measures of trial protocol and intervention feasibility and acceptability: physician study and visit perceived burden, patient satisfaction, and patient, physician and staff experience with the trial. Additional measurements of intervention impact include: initial estimates of effect size on patient treatment burden and other patient-oriented outcomes, change in glycemic control, and other intermediate medical outcomes.
This intervention is novel as it collects patient life context information using a direct person-to-person approach, allows physicians to review the information prior to patient arrival at the clinic and, where appropriate, incorporate it when negotiating treatment plans, and is longitudinal, summarizing evolving contextual information over time. This pilot RCT has the potential to demonstrate trial protocol and intervention feasibility and acceptability, and estimate effect size on patient and provider outcomes, to inform for a future, definitive RCT.Trial Registration: This trial was registered at ClinicalTrials.gov prior to patient enrollment: NCT04568382.
多种疾病并存的情况很常见,患者的生活背景会影响医疗护理。旨在改善以患者为中心的结局(如感知到的治疗负担)的有效且高效的干预措施有限。需要将患者背景信息整合到初级医疗服务中的干预措施,以改善此类结局。患者生活背景是影响患者生活和医疗保健的众多因素,包括健康的社会决定因素以及家庭和工作需求等更广泛的因素。
本试点随机对照试验(RCT)方案将比较针对患有糖尿病及其他慢性合并症患者的标准就诊前规划与纳入患者生活背景的就诊前规划。主要结局包括试验方案及干预措施的可行性和可接受性指标:医生对研究和就诊的感知负担、患者满意度,以及患者、医生和工作人员对试验的体验。干预措施影响的其他测量指标包括:对患者治疗负担及其他以患者为导向的结局的效应大小的初步估计、血糖控制的变化以及其他中间医疗结局。
该干预措施具有创新性,因为它采用直接的人际交流方式收集患者生活背景信息,允许医生在患者到达诊所之前查看信息,并在协商治疗方案时酌情纳入这些信息,而且是纵向的,会总结随时间变化的背景信息。这项试点RCT有可能证明试验方案及干预措施的可行性和可接受性,并估计对患者和提供者结局的效应大小,为未来的确定性RCT提供参考。试验注册:本试验在患者入组前已在ClinicalTrials.gov上注册:NCT04568382。