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Smart Phone Application for Enteral Nutrition

University of Oklahoma (OU) logo

University of Oklahoma (OU)

Status

Completed

Conditions

Nutritional and Metabolic Diseases

Treatments

Other: Tube Feeding Application

Study type

Observational

Funder types

Other

Identifiers

NCT03419299
OU 4496

Details and patient eligibility

About

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.

Full description

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.

Enrollment

376 patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Admitted to the ICU
  2. Require Mechanical Ventilation
  3. Physician plans to order enteral nutrition for the patient

Exclusion criteria

  1. Death likely within 24 hours
  2. Needing parenteral nutrition
  3. Cannot tolerate enteral nutrition for any reason

Trial design

376 participants in 2 patient groups

Pre- Application
Description:
Patients admitted prior to use of tube feeding application
Post- Application
Description:
Patients admitted when tube feeding application was being used.
Treatment:
Other: Tube Feeding Application

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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