IBDPROMISE: A Web-based Patient-centric Model to Improve Quality and Outcomes

IBDPROMISE：基于网络的以患者为中心的模型，用于提高质量和结果

• 批准号: 9144365
• 负责人: Ashish Atreja
• 金额: $ 17.75万
• 依托单位: ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI
• 依托单位国家: 美国
• 财政年份: 2013
• 资助国家: 美国
• 起止时间: 2013-09-16 至 2018-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9144365
• 关键词: Address; Adoption; Adult; Affect; Blood Pressure; Caring; Clinical; Clinical Trials Design; Cohort Studies; Colonoscopy; Communities; Computer Literacy; Consent; Cost Savings; Crohn' s disease; Data; Decision Making; Demographic Impact; Devices; Diabetes Mellitus; Dimensions; Disease; Disease Management; Drops; Economics; Effectiveness; Electronic Health Record; Electronics; Emotional; Enrollment; Evaluation; Focus Groups; Future; Goals; Graph; Health; Health Care Reform; Hemoglobin; Home environment; Hospitals; Hypertension; Immunization; Inflammatory Bowel Diseases; Institution; Lead; Learning; Licensing; Measurement; Measures; Medical; Methods; Modeling; Monitor; Multi-Institutional Clinical Trial; Office Visits; Online Systems; Outcome; Participant; Patient Outcomes Assessments; Patient-Focused Outcomes; Patients; Personal Satisfaction; Phenotype; Physicians; Provider; Quality Indicator; Quality of Care; Quality of life; Questionnaires; Randomized Controlled Trials; Recommendation; Recording of previous events; Report (document); Reporting; Resources; Risk; Self Management; Severities; Severity of illness; Site; Societies; Socioeconomic Status; Stratification; Structure; Surveys; Tablets; Time; Ulcerative Colitis; Work; arm; base; compliance behavior; cost; cost effective; cost effectiveness; dashboard; design; disease phenotype; disorder control; eHealth; health care quality; health care service utilization; improved; improved outcome; literacy; meetings; point of care; primary outcome; prospective; skills; social; tertiary care; trend; web-enabled

DESCRIPTION (provided by applicant): Background: Measuring and improving healthcare quality is an important national challenge. The discussion about quality and disease management rarely happens during office visits when patients and providers have a unique opportunity to listen to each other and make collaborative decisions. Hypothesis: Encouraging patients to proactively measure and improve quality can bring remarkable efficiency, effectiveness and cost-savings to quality improvement efforts. Goal: To acquire skills to design and evaluate a patient-centric model, IBDPROMISE (IBD Patient Reported Outcomes and Medical IIlness Severity Evaluation), in which patients with inflammatory bowel disease (IBD) measure their quality of care metrics (such as colonoscopy surveillance) as well as quality of life in waiting rooms and at home; and physicians use this information at the point of care for quality improvement efforts. The specific aims of the project are: " AIM I. Define a set of comprehensive quality of care metrics (such as immunization, appropriate colonoscopy surveillance) for IBD patients from national recommendations. " AIM II. Measure longitudinally quality of care metrics and quality of life (QOL). "AIM III. Conduct a randomized controlled trial to determine the impact of IBDPROMISE in improving outcomes (quality of care, quality of life, patient adherence, disease control and resource utilization). Methods: All eligible adult patients arriving in Mount Sinai Hospital IBD center and a community site during study recruitment will be offered tablet-based questionnaire in waiting rooms and enrolled once consented. After a baseline period (at least six months), participants in the IBDPROMISE arm will be asked to report their quality of care metrics and QOL every month for 18 months. This will generate an electronic health card (detailing disease summary, quality metrics and a graph showing the trend of QOL and healthcare utilization over time). Patients and providers will use the health card, active decision support (a drop in scores) and passive decision support (quality dashboards and reminders) to improve the quality of care collaboratively. Outcome: The primary end-point of the study is the proportion of patients in each group (IBDPROMISE vs. control) who meet all eligible quality metrics at week 104. Secondary endpoints will be comparison of quality of life, disease control rates and utilization of healthcare resources between the two arms. Additional analysis will be done to determine the impact of demographics, socioeconomic status and computer literacy on IBDPROMISE adoption and improvement in outcomes. Future Direction: This project will help me acquire critical skills in self-management, quality improvement, design of clinical trials and analysis of quality of life data and cost effectiveness. In the future, IBDPROMISE and its point of care QI model within EHR, if proven successful, will be made available license-free to other academic institutions, and help me implement multi-site clinical trials and prospective cohort studies in IBD.

描述（由申请人提供）：背景：衡量和提高医疗质量是一个重要的国家挑战。关于质量和疾病管理的讨论很少发生在办公室访问期间，当患者和提供者有一个独特的机会互相倾听并做出合作决定时。假设：鼓励患者主动测量和改进质量可以为质量改进工作带来显着的效率，有效性和成本节约。目标：获得设计和评价以患者为中心的模型IBDPROMISE（IBD患者报告结局和医学疾病严重程度评价）的技能，其中炎症性肠病（IBD）患者测量其护理指标质量（如结肠镜检查监测）以及生活质量 在候诊室和家里;医生在护理点使用这些信息进行质量改进。该项目的具体目标是：“AIM I。根据国家建议，为IBD患者定义一套全面的护理质量指标（如免疫接种、适当的结肠镜检查监测）。 “AIM II.纵向测量护理质量指标和生活质量（QOL）。 “AIM III.进行随机对照试验 确定IBDPROMISE在改善结局（护理质量、生活质量、患者依从性、疾病控制和资源利用）方面的影响。研究方法：在研究招募期间到达西奈山医院IBD中心和社区研究中心的所有合格成人患者将在候诊室获得基于平板电脑的问卷，并在获得知情同意后入组。在基线期（至少6个月）后，将要求IBDPROMISE组的参与者每月报告他们的护理质量指标和QOL，持续18个月。这将生成一张电子健康卡（详细说明疾病摘要、质量指标和显示QOL和医疗保健利用率随时间变化趋势的图表）。患者和医疗服务提供者将使用健康卡、主动决策支持（分数下降）和被动决策支持（质量仪表板和提醒）来协同提高护理质量。结果：研究的主要终点是第104周时每组（IBDPROMISE vs.对照组）中符合所有合格质量指标的患者比例。次要终点将是两组之间的生活质量、疾病控制率和医疗资源利用的比较。将进行额外的分析，以确定人口统计学，社会经济地位和计算机素养对IBDPROMISE采用和改善结果的影响。未来方向：这个项目将帮助我获得自我管理，质量改进，临床试验设计和生活质量数据和成本效益分析的关键技能。 在未来，如果IBDPROMISE及其在EHR中的床旁QI模型被证明是成功的，将免费提供给其他学术机构，并帮助我在IBD中实施多中心临床试验和前瞻性队列研究。