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OpenTrials
Completed

NCT Number: NCT03419299

Smart Phone Application for Enteral Nutrition

Internal medicine resident physicians were provided an ipod with the EN application to assist them in choosing EN formulas for patients during their ICU rotation. The primary outcome was improved initiation of EN within 24 hours of admission. Secondary outcomes include, time to initiate EN, goal calories reached, infections rates, length of stay, mortality, and concordance with clinical guidelines.

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Key information

Age range

18 year–90 year

Sex eligibility

All sexes

Study type

Observational

About this study

Background: Resident physicians are frequently uncomfortable ordering enteral nutrition (EN) and are unaware of the variety of formulas and supplements available for different disease processes. Many depend on a clinical dietitian to assist with recommending EN formulas and patient energy requirements which may not be readily available upon patient admission. This creates a barrier to early initiation of EN and non-compliance with Society of Critical Care Medicine and American Society of Parenteral and Enteral Nutrition clinical guidelines. Objective: Internal medicine resident physicians were provided an ipod with the EN application to assist them in choosing EN formulas for patients during their ICU rotation. The primary outcome was improved initiation of EN within 24 hours of admission. Secondary outcomes include, time to initiate EN, goal calories reached. Design: This study is a retrospective chart review to evaluate the impact of a smart phone/device application (EN application) to assist resident physicians when ordering EN. The study is a single center trial conducted at an academic teaching facility. All patient data was obtained by a retrospective chart review of patients admitted to the intensive care unit (ICU) at The University of Oklahoma Medical Center.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Admitted to the ICU
  • Require Mechanical Ventilation
  • Physician plans to order enteral nutrition for the patient

Exclusion criteria

  • Death likely within 24 hours
  • Needing parenteral nutrition
  • Cannot tolerate enteral nutrition for any reason

Treatment and study plan

Tube Feeding Application

Other

A smart device application was developed and used to help residents determine the best enteral nutrition prescription for patients admitted to the ICU

Primary outcomes

  1. The primary outcome was improved initiation of EN within 24 hours of admission

    Time frame: The time frame does involve a change in practice. The change is introduction of a smart app- 12 months prior to the smart device being used in the ICU by residents and 12 months during which the smart application was use by the ICU residents

    percent of patients with enteral nutrition ordered within 24 hours of admit compared to all patients admitted

Secondary outcomes

  1. Total time to initiate EN

    Time frame: The time frame does involve a change in practice. The change is introduction of a smart app- 12 months prior to the smart device being used in the ICU by residents and 12 months during which the smart application was use by the ICU residents

    total hours between admit and when enteral nutrition is ordered

  2. Percent of goal calories received prior to discharge from ICU

    Time frame: The time frame does involve a change in practice. The change is introduction of a smart app- 12 months prior to the smart device being used in the ICU by residents and 12 months during which the smart application was use by the ICU residents

    percent of calories received (a percent of the total recommended calories for the patient)

Sponsors and collaborators

Lead sponsor

University of Oklahoma

Other

Registry information

Official study title

Smart Phone/Device Application to Improve Delivery of Enteral Nutrition in Adult Patients Admitted to the Medical Intensive Care Unit

Important dates

Study start
2015
Primary completion
2017
Study completion
2017
First posted
Feb 1, 2018
Registry last updated
Jun 12, 2019

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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