Loyola University Medical Center
Maywood, Illinois, 60153, United States
NCT Number: NCT01987141
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.
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Notify Me18 year and older
Female
Interventional
Not applicable
Maywood, Illinois, 60153, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Electronic medical record flag/notification in the patient's chart
Time frame: 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)
Time frame: At end of pregnancy, average of 40 weeks from enrollment
Survey to patients at the end of pregnancy regarding how patients perceive and are influenced by EMR notifications and counseling
Loyola University
Other
WATE Study - Gestational Weight Gain and the Electronic Medical Record
Acronym: WATE
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