A widespread self-management education program to reduce health disparities in African American women with systemic lupus erythematosus

一项广泛的自我管理教育计划，旨在减少患有系统性红斑狼疮的非裔美国女性的健康差异

• 批准号: 9481199
• 负责人: Cristina Marta Drenkard
• 金额: $ 39万
• 依托单位: EMORY UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2016
• 资助国家: 美国
• 起止时间: 2016-08-23 至 2021-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9481199
• 关键词: Accident and Emergency department; Address; Adult; Affect; Affordable Care Act; African American; Age; Anxiety; Arthritis; Behavior; Characteristics; Charge; Chronic; Chronic Disease; Client; Clinical; Communication; Communities; Complex; Data; Databases; Degenerative polyarthritis; Diabetes Mellitus; Disease; Disease Management; Education; Effectiveness; Emergency department visit; Emotions; Enrollment; Exercise; Family; Fatigue; Female of child bearing age; Goals; Health; Health Services; Health Status; Health behavior change; Health education; Health system; Healthcare; Healthy Eating; Hospitalization; Individual; Intervention; Intervention Studies; Interview; Learning; Link; Longitudinal cohort; Low income; Lupus; Measures; Medical; Medication Management; Mental Depression; Outcome; Pain; Parents; Participant; Patients; Personal Satisfaction; Pilot Projects; Policies; Population; Prevalence; Problem Solving; Process; Reporting; Resources; Rheumatology; Sampling; Self Care; Self Efficacy; Self Management; State Hospitals; Symptoms; Systemic Lupus Erythematosus; Testing; Time; Visit; Woman; barrier to care; base; care outcomes; chronic autoimmune disease; cohort; community center; comorbid depression; design; ethnic minority population; evidence base; experience; health care availability; health care service utilization; health disparity; health related quality of life; health service use; high risk; improved; improved outcome; medication compliance; mortality; multiple chronic conditions; novel; pain reduction; peer; physical conditioning; population based; post intervention; programs; psychosocial; public health relevance; recruit; self-management program; skills; social; socioeconomics; symptom management; tool; treatment as usual

 DESCRIPTION (provided by applicant): Systemic lupus erythematosus (SLE) is a chronic disease that primarily strikes young African American women. Prevalence is three times higher for African American than White women, and patients from ethnic minorities are at the highest risk for comorbidities, depression, poor health, and mortality. SLE patients must engage in challenging self-management activities to promote their wellbeing and efficiently use health care services. Because effectively self-managing chronic conditions requires skills that are often related to health education, self-management support is one of the top priorities of the US health system. Unlike for other chronic illnesses such as arthritis and diabetes, there are no widely disseminated, evidence-based SLE-specific self-management resources. The proposed study will examine whether an established self-management program for people with chronic illnesses, the Chronic Disease Self-management Program (CDSMP), can improve fundamental self- management behaviors and reduce the negative medical and psychosocial consequences of SLE among AA women. The CDSMP is a broadly available small group-based program delivered in the community as an effective tool for improving self-management behaviors and health outcomes, and for decreasing health care utilization in people with chronic diseases. Designed to address health issues that cut across different conditions (e.g., pain, fatigue, anxiety), the CDSMP may represent a suitable option for African American with SLE, with the advantage of its wide dissemination. As the CDSMP has been primarily evaluated in samples predominantly represented by white middle class seniors with more common diseases (e.g. osteoarthritis, diabetes), the effectiveness of the CDSMP in helping AAs women to self-manage SLE is unknown. This study aims to assess the effectiveness and cultural relevance of the CDSMP in African American women with SLE. Participants will be recruited from the Georgians Organized Against Lupus (GOAL), a population-based cohort of individuals with SLE with the full clinical spectrum and from broad socioeconomic background. A random sample of 150 African American women will attend the CDSMP in their communities, along with people with other diseases. Twelve- and 18-month changes of health behaviors, health status, and health services utilization will be compared between CDSMP participants and African American women with SLE receiving usual care. Differential effects of the CDSMP on outcomes by sociodemographic and health factors will be examined. A longitudinal qualitative study will assess the impact of the CDSMP on women's definitions and experiences related to self-management, health and health service utilization. The potential for immediate large-scale implementation of the CDSMP to a large segment of the SLE population that is at high-risk for poor outcomes may contribute to reduce health disparities.

 描述（由申请人提供）：系统性红斑狼疮（SLE）是一种慢性疾病，主要打击年轻的非洲裔美国妇女。非裔美国人的患病率是白色妇女的三倍，少数民族患者患合并症、抑郁症、健康状况不佳和死亡率的风险最高。 SLE患者必须参与具有挑战性的自我管理活动，以促进他们的健康并有效地利用医疗保健服务。由于有效地自我管理慢性病需要通常与健康教育相关的技能，因此自我管理支持是美国卫生系统的首要任务之一。与关节炎和糖尿病等其他慢性疾病不同，没有广泛传播的、基于证据的SLE特异性自我管理资源。 拟议的研究将检查慢性病患者的既定自我管理计划，慢性病自我管理计划（CDSMP），是否可以改善基本的自我管理行为，减少AA女性中SLE的负面医疗和心理社会后果。 CDSMP是一个广泛提供的小团体为基础的计划，在社区提供作为一个有效的工具，改善自我管理行为和健康结果，并减少慢性病患者的医疗保健利用。旨在解决跨越不同条件的健康问题（例如，疼痛，疲劳，焦虑），CDSMP可能是一个合适的选择，非洲裔美国人与SLE，其广泛传播的优势。由于CDSMP主要在以患有更常见疾病（如骨关节炎、糖尿病）的白色中产阶级老年人为代表的样本中进行了评价，因此CDSMP在帮助AA女性自我管理SLE方面的有效性尚不清楚。本研究旨在评估CDSMP在非裔美国女性SLE患者中的有效性和文化相关性。 参与者将从格鲁吉亚组织抗狼疮（GOAL）招募，这是一个基于人群的SLE患者队列，具有完整的临床谱和广泛的社会经济背景。随机抽样的150名非洲裔美国妇女将参加CDSMP在他们的社区，沿着与其他疾病的人。12个月和18个月的健康行为，健康状况和卫生服务利用的变化将比较CDSMP参与者和非裔美国女性SLE接受常规护理。将研究CDSMP对社会人口学和健康因素结果的不同影响。一项纵向定性研究将评估CDSMP对妇女自我管理、保健和保健服务利用方面的定义和经验的影响。 对大部分SLE患者立即大规模实施CDSMP的可能性可能有助于减少健康差异。