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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
Massachusetts General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

    First Posted
    October 27, 2014
    Last Updated
    January 31, 2017
    Sponsor
    Massachusetts General Hospital
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    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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