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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02277535
Other study ID # 2014P001702
Secondary ID
Status Completed
Phase N/A
First received October 27, 2014
Last updated January 31, 2017
Start date December 2014
Est. completion date April 2015

Study information

Verified date January 2017
Source Massachusetts General Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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


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.


Recruitment information / eligibility

Status Completed
Enrollment 197
Est. completion date April 2015
Est. primary completion date April 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Feedback/Reminder email.


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Massachusetts General Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary 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 After completing the intervention for each ICU (2 months)
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