跳至主要内容
临床试验/NCT03473509
NCT03473509已完成不适用

Impact of a Safety-Net Primary Care CKD Registry

University of California, San Francisco0 个研究点目标入组 746 人开始时间: 2013年6月最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
746
主要终点
Change in clinic systolic

研究概览

简要总结

This study examines whether a safety-net primary care CKD registry directed at the entire primary care team can enhance the delivery of guideline concordant CKD care, including BP control, ACEi/ARB use and albuminuria quantification.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All PCPs who worked in practice teams and provided longitudinal primary care to patients were eligible to participate in this study. Practice teams that consisted of several physicians (+/- trainees), one nurse, nurse practitioners, medical assistants and behaviorists, were randomized 1:1 to one of two arms with a random number generator: access to an electronic CKD registry or a usual care registry for 12 months.

排除标准

  • PCPs who solely provided specialty care, for example HIV services or urgent care, were excluded.

研究组 & 干预措施

Chronic Kidney Disease (CKD) Registry

Experimental

The CKD registry provided primary care practice teams with point-of-care data about patient-specific CKD status, recent ambulatory clinic blood pressure (BP) readings, status of Angiotensin Converting Enzyme inhibitor (ACEi) or Angiotensin Receptor Blocker (ARB) prescription, and quantification of albuminuria (UACR). It also provided data about diabetes care, immunization status, and data pertinent to age appropriate cancer screening, to align with usual care. Point-of-care decision support reminded primary care providers (PCPs) about guideline concordant care for individuals with CKD. Quarterly feedback to practice teams and individual PCPs identified patients with CKD and BP >140/90 mmHg, those not prescribed an ACEi/ARB, and those with albuminuria.

干预措施: CKD Registry (Other)

Usual Care Registry

No Intervention

Usual care consisted of an electronic registry that was in use before trial implementation. It provided practice teams with point-of-care data about diabetes care, age-appropriate cancer screening and immunizations, but no CKD-related data. Medical assistants were encouraged to use the usual care registry to identify patients who were due for cancer screening or immunizations. Quarterly feedback was not provided for practice teams randomized to receive usual care.

结局指标

主要结局

Change in clinic systolic

时间窗: 12 months

Change in ambulatory systolic BP measured at ambulatory clinic visits in the health care system.

次要结局

  • Change in proportion fo patients with urine albuminuria quantification(12 months)
  • Change in proportion of patients with BP control(12 months)
  • Change in proportion of patients with ACEi/ARB prescription(12 months)
  • Change in albuminuria severity(12 months)

研究者

申办方类型
Other
责任方
Sponsor

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