跳至主要内容
临床试验/NCT00251875
NCT00251875Unknown不适用

Shared Online Health Records for Patient Safety and Care

Agency for Healthcare Research and Quality (AHRQ)10 个研究点 分布在 1 个国家目标入组 5,400 人开始时间: 2005年7月1日最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
5,400
试验地点
10
主要终点
1. ADEs

研究概览

简要总结

The study uses a randomized, prospective cohort design to assess the impact of shared online health records on 1) patient safety, 2) health goal adherence and outcomes, 3) documentation of family history, and 4) barriers to the adoption of patient-physician communication technology.

Hypothesis: the respective interventions will result in 1) improved patient safety 2) greater adherence to health care maintenance and chronic disease guidelines 3) more accurate documentation of family history 4) the identification of technology adoption enablers and barriers.

详细描述

During the first phase of the study, primary care practice patients continue to receive "usual care" while their physician's offices are using Patient Gateway, an Internet portal offering secure messaging, common requests, chart information, and health information that has already been developed. Also in this first phase, all patients using Patient Gateway will receive an electronic letter explaining the research study and a link to an electronic consent form. In addition to recruitment of subjects, phase 1 allows for baseline data to be collected.

In the second phase, study clinics will be randomized into one of two intervention "arms". Study subjects whose clinics are randomized into Arm 1 will be invited to review and comment on their medication, allergy, and diabetes information through Patient Gateway; they can then submit this information to their primary care physician for review. Those randomized into Arm 2 will report on their health maintenance status and family history and submit this information to their primary care physician through Patient Gateway prior to a scheduled visit. Chart reviews performed at the end of Phase 1 and Phase 2 will be conducted to identify differences in process measures and outcome measures between intervention and control groups.

In addition, a medication phone survey sub-study will be conducted to evaluate the effect of the new Patient Gateway features on medication management.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

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

入选标准

  • •All patients, who are enrolled in Patient Gateway, of physicians and practices participating in the study.

排除标准

  • •Any patients who are not enrolled in Patient Gateway or do not belong to a participating practice.

结局指标

主要结局

1. ADEs

2. duration of ameliorable medication side effects

3. health goal adherence rates

4. diabetes outcomes

5. familial risk factor documentation rates

6. user satisfaction surveys

7. user metrics

次要结局

未报告次要终点

研究者

发起方
Agency for Healthcare Research and Quality (AHRQ)
申办方类型
Fed

研究点 (10)

Loading locations...

相似试验