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More-2-Eat; Implementation of INPAC (m2E)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT02800304
Recruitment Status : Completed
First Posted : June 15, 2016
Last Update Posted : February 5, 2019
Sponsor:
Collaborator:
University of Western Ontario, Canada
Information provided by (Responsible Party):
Heather Keller, University of Waterloo

Brief Summary:
M2E is a developmental evaluation of the implementation of the Integrated Nutrition Pathway for Acute Care, in five medical units in five hospitals in Canada.

Condition or disease
Acute Care Medical

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Study Type : Observational
Actual Enrollment : 5995 participants
Observational Model: Cohort
Time Perspective: Prospective
Study Start Date : September 1, 2015
Actual Primary Completion Date : March 31, 2017
Actual Study Completion Date : March 31, 2017

Resource links provided by the National Library of Medicine





Primary Outcome Measures :
  1. Implementation success of Integrated Nutrition Pathway for Acute Care (INPAC) [ Time Frame: admission ]
    INPAC is an evidence based pathway to improve detection, prevention and treatment of malnutrition in acute care. The primary outcome of this study is the trajectory and proportion of care activities that happen for a given population e.g. % screened, assessed with SGA, have standard care strategies provided etc.



Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population
medical patients over the age of 18 years
Criteria

Inclusion Criteria:

  • admitted to study unit
  • no delirium or dementia
  • return to community anticipated

Exclusion Criteria:

  • unable to communicate in English or French

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT02800304


Locations
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Canada, Alberta
Royal Alexander Hospital
Edmonton, Alberta, Canada
Canada, Manitoba
Concordia Hospital
Winnipeg, Manitoba, Canada
Canada, Ontario
Niagara Health Systems
Niagara Falls, Ontario, Canada
The Ottawa Hospital
Ottawa, Ontario, Canada
Canada, Saskatchewan
Pasqua Hospital
Regina, Saskatchewan, Canada
Sponsors and Collaborators
University of Waterloo
University of Western Ontario, Canada
Investigators
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Principal Investigator: Heather Keller, PhD University of Waterloo
  Study Documents (Full-Text)

Documents provided by Heather Keller, University of Waterloo:
Study Protocol  [PDF] June 1, 2017

Additional Information:
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

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Responsible Party: Heather Keller, Research Chair, Nutrition & Aging, University of Waterloo
ClinicalTrials.gov Identifier: NCT02800304    
Other Study ID Numbers: 20590
First Posted: June 15, 2016    Key Record Dates
Last Update Posted: February 5, 2019
Last Verified: February 2019
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No
Keywords provided by Heather Keller, University of Waterloo:
malnutrition
food intake
frailty