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OpenTrials
Completed

NCT Number: NCT01987141

Gestational Weight Gain and the Electronic Medical Record

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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Key information

Age range

18 year and older

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Loyola University Medical Center

Maywood, Illinois, 60153, United States

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

EMR Intervention

Other

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

Primary outcomes

  1. Weight gain

    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)

Secondary outcomes

  1. Patient perception

    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

Sponsors and collaborators

Lead sponsor

Loyola University

Other

Registry information

Official study title

WATE Study - Gestational Weight Gain and the Electronic Medical Record

Acronym: WATE

Important dates

Study start
2013
Primary completion
2014
Study completion
2016
First posted
Nov 19, 2013
Registry last updated
May 12, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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