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临床试验/NCT01987141
NCT01987141已完成不适用

WATE Study - Gestational Weight Gain and the Electronic Medical Record

Loyola University2 个研究点 分布在 1 个国家目标入组 150 人开始时间: 2013年10月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
150
试验地点
2
主要终点
Weight gain

研究概览

简要总结

Less than one third of pregnant women actually achieve the Institute of Medicine's (IOM) recommended weight gain. To date, there are no randomized controlled trials studying the use of the electronic medical record to alert providers to initiate the counseling of patients on the IOM gestational weight gain recommendations.

In the investigator's planned study intervention, using the EPIC EMR system, an electronic alert (Best Practice Advisory) will appear for providers at each prenatal care visit. This alert will remind providers to counsel patients on the recommendations for gestational weight gain. The control group will receive standard prenatal care, without electronic alerts generated regarding BMI and gestational weight gain.

The investigators hypothesize that a higher percentage of patients who receive the intervention will meet the IOM guidelines for weight gain.

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
None

入排标准

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

入选标准

  • Pregnant with a single intrauterine gestation
  • Present for new OB visit up to 13 weeks and 6 days gestation

排除标准

  • They have a multiple gestation pregnancy
  • They are under the age of 18
  • They do not speak English

结局指标

主要结局

Weight gain

时间窗: At delivery, average of 40 weeks from enrollment

Primary outcome will be measured as the percent of patients who achieve their recommended weight gain goal in pregnancy (IOM guidelines)

次要结局

  • Patient perception(At end of pregnancy, average of 40 weeks from enrollment)

研究者

发起方
Loyola University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Scott Graziano

Associate Professor

Loyola University

研究点 (2)

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