Decreasing Medication Errors by Caregivers Using a Health Literacy Intervention
2015年4月23日 更新者:Columbia University
Giving medications to children can be confusing; studies have shown that caregivers make dosing administration errors up to 50% of the time.
There are many reasons that there are so many errors, including the fact that dosing for children is based on their weight, liquid medications come in many different forms, and caregivers often give medicines using kitchen teaspoons and tablespoons.
Caregivers who have difficulty reading have even more difficulty understanding medication instructions.
We are developing and testing a web-based educational module to teach caregivers how to give medications.
We are focusing on the pediatric emergency department because we know that this population has low literacy levels, and that many antibiotics are prescribed in this setting.
We anticipate that those caregivers that view the interactive module will have increased knowledge on how to give medications once they get home.
研究概览
详细说明
Dosing error rates of home administration of medications to children have been reported to be as high as 50%.
Contributing to this error rate are the complexity of pediatric weight-based dosing, confusing formulations of liquid medications, and a reliance on non-standardized dosing tools such as kitchen teaspoons and tablespoons to administer medications.
Families with low health literacy are at particular risk for medication administration errors.
Health literacy promoting interventions to improve medication administration such as dissemination of a pictogram-based medication list have been shown to work for common over-the-counter medications such as acetaminophen, but their effect on administration practices for common medications prescribed in the pediatric emergency department (PED) has not been evaluated.
Of the 50,000 patients seen in the PED each year, approximately 85% of patients are discharged with a prescription for medication.
This makes the PED an ideal setting to implement a health literacy intervention to reduce medication administration errors at home.
The investigators are proposing to conduct a randomized controlled trial of an educational module focused on how to administer antibiotics at home and test whether there is an improvement in care practices.
研究类型
介入性
注册 (实际的)
132
阶段
- 不适用
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
-
-
New York
-
New York、New York、美国、10032
- Columbia University Medical Center
-
-
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
2个月 至 8年 (孩子)
接受健康志愿者
不
有资格学习的性别
全部
描述
Inclusion Criteria:
Caregivers of:
- Patients aged 2 months to 8 years
- Patients triaged to Emergency Severity Index (ESI) level 4 or 5 in the pediatric emergency department.
- Patients with at least one prescription for a liquid, tablet or ointment antibiotic.
Exclusion Criteria:
Caregivers of:
- Patients in need of immediate care.
- Patients hospitalized.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:卫生服务研究
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:单身的
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:Fever assessment and management
Medication administration educational module for low literacy subjects on how to administer common medications appropriately and safely.
|
The Research Assistant (RA) will enter the subject's language (English or Spanish), the type of medicine (tablet/capsule, liquid, or ointment) from the antibiotic prescription, and the frequency (once a day, twice a day, three times a day, four times a day) from the antibiotic prescription into the web-based educational module on medication administration so that a tailored module will be setup for the subject.
The subject will then view the educational interactive module.
After the subject is done with the module, the RA will administer a verbal post-test.
The post-test will include questions on medication administration as well as questions on fever assessment and management.
其他名称:
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Score on the telephone interview post-test
大体时间:48-72 hours post Emergency Department visit
|
Subject scores will be dichotomized in the follow way: anything less than 100% will be considered incorrect, a score of 100% will be considered correct.
|
48-72 hours post Emergency Department visit
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Prevalence of perfect performance on each element of the questionnaire
大体时间:48-72 hours post Emergency Department visit
|
Each answer on the telephone interview post-test will be dichotomized into a correct/incorrect answer.
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48-72 hours post Emergency Department visit
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合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
调查人员
- 首席研究员:Anupama Subramony, MD, MBA、Columbia University
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2011年2月1日
初级完成 (实际的)
2013年1月1日
研究完成 (实际的)
2013年1月1日
研究注册日期
首次提交
2011年2月4日
首先提交符合 QC 标准的
2011年2月10日
首次发布 (估计)
2011年2月11日
研究记录更新
最后更新发布 (估计)
2015年4月24日
上次提交的符合 QC 标准的更新
2015年4月23日
最后验证
2015年4月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.