An Email Intervention to Prevent Iatrogenic Malnutrition in the ICU
Primary Purpose
Malnutrition
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Feedback/Reminder email.
Sponsored by
About this trial
This is an interventional prevention trial for Malnutrition focused on measuring Malnutrition in the ICU (caloric deficit >4000 kcal or 150 g protein deficit) or >48hrs of admission without receiving nutrition
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.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
E-mail intervention
No E-mail intervention
Arm Description
ICU clinicians caring for patients who have not yet been initiated on nutrition 48 hours after ICU admission will receive a reminder email. ICU clinicians caring for patients who accumulate a caloric deficit greater than 4000 calories or 150 g protein deficit will receive a feedback email
Nutrition status of patients will be assessed but no reminder or feedback emails will be sent
Outcomes
Primary Outcome Measures
Patients started on nutrition within 72 h of ICU admission
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
Secondary Outcome Measures
Full Information
NCT ID
NCT02277535
First Posted
October 27, 2014
Last Updated
January 31, 2017
Sponsor
Massachusetts General Hospital
1. Study Identification
Unique Protocol Identification Number
NCT02277535
Brief Title
An Email Intervention to Prevent Iatrogenic Malnutrition in the ICU
Official Title
An Email Intervention to Prevent Iatrogenic Malnutrition in the ICU
Study Type
Interventional
2. Study Status
Record Verification Date
January 2017
Overall Recruitment Status
Completed
Study Start Date
December 2014 (undefined)
Primary Completion Date
April 2015 (Actual)
Study Completion Date
April 2015 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Massachusetts General Hospital
4. Oversight
Data Monitoring Committee
No
5. Study Description
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malnutrition
Keywords
Malnutrition in the ICU (caloric deficit >4000 kcal or 150 g protein deficit) or >48hrs of admission without receiving nutrition
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
197 (Actual)
8. Arms, Groups, and Interventions
Arm Title
E-mail intervention
Arm Type
Experimental
Arm Description
ICU clinicians caring for patients who have not yet been initiated on nutrition 48 hours after ICU admission will receive a reminder email.
ICU clinicians caring for patients who accumulate a caloric deficit greater than 4000 calories or 150 g protein deficit will receive a feedback email
Arm Title
No E-mail intervention
Arm Type
No Intervention
Arm Description
Nutrition status of patients will be assessed but no reminder or feedback emails will be sent
Intervention Type
Other
Intervention Name(s)
Feedback/Reminder email.
Primary Outcome Measure Information:
Title
Patients started on nutrition within 72 h of ICU admission
Description
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
Time Frame
After completing the intervention for each ICU (2 months)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
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.
12. IPD Sharing Statement
Learn more about this trial
An Email Intervention to Prevent Iatrogenic Malnutrition in the ICU
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