Skip to content

Gestational Weight Gain and the Electronic Medical Record

WATE Study - Gestational Weight Gain and the Electronic Medical Record

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01987141
Acronym
WATE
Enrollment
150
Registered
2013-11-19
Start date
2013-10-31
Completion date
2016-05-31
Last updated
2016-05-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancy, Weight Gain

Brief summary

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.

Interventions

OTHEREMR Intervention

Electronic medical record flag/notification in the patient's chart

Sponsors

Loyola University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frameDescription
Weight gainAt delivery, average of 40 weeks from enrollmentPrimary outcome will be measured as the percent of patients who achieve their recommended weight gain goal in pregnancy (IOM guidelines)

Secondary

MeasureTime frameDescription
Patient perceptionAt end of pregnancy, average of 40 weeks from enrollmentSurvey to patients at the end of pregnancy regarding how patients perceive and are influenced by EMR notifications and counseling

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026