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Clinical Trials/NCT02277535
NCT02277535
Completed
Not Applicable

An Email Intervention to Prevent Iatrogenic Malnutrition in the ICU

Massachusetts General Hospital0 sites197 target enrollmentDecember 2014
ConditionsMalnutrition

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Malnutrition
Sponsor
Massachusetts General Hospital
Enrollment
197
Primary Endpoint
Patients started on nutrition within 72 h of ICU admission
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

This is a quality improvement research project evaluating if a targeted feedback email to clinicians impacts their nutrition delivery in the ICU.

Detailed Description

This prospective study looks to determine if a targeted email to clinicians taking care of critically ill patients will allow reduce malnutrition in the Intensive Care Units (ICU). Four ICUs will be included: medical ICU (MICU), coronary care unit (CCU) and two surgical ICUs. The investigators will rotate a 2 month period intervention amongst the aforementioned participating ICUs and follow simultaneous cohorts to evaluate the effect of our intervention (email feedback to treating clinicians) on nutrition delivery in the ICU. After the completion of the intervention, there will be a six-month follow-up of nutritional adequacy to assess the durability of changes in behavior.

Registry
clinicaltrials.gov
Start Date
December 2014
End Date
April 2015
Last Updated
9 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Daniel Dante Yeh

Trauma and Critical Care Surgeon

Massachusetts General Hospital

Eligibility Criteria

Inclusion Criteria

  • Clinicians taking care of patients admitted to the ICU within the past 48hrs
  • Clinicians taking care of patients in whom enteral nutrition is prescribed

Exclusion Criteria

  • Clinicians taking care of patients in whom enteral nutrition is not prescribed.

Outcomes

Primary Outcomes

Patients started on nutrition within 72 h of ICU admission

Time Frame: After completing the intervention for each ICU (2 months)

The ICU admission date and EN initiation date will be collected in a data base which will later be analyzed to assess the percentange of patients initiated on EN within 72 hours of admission to the ICU. This will be reported as rates and will be compared amongst intervention and no-intervention arms using Fisher's Exact test or Chi-sq Test

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