We are updating the design of this site. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

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

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT02800304
First Posted: June 15, 2016
Last Update Posted: April 19, 2017
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.
Collaborator:
University of Western Ontario, Canada
Information provided by (Responsible Party):
Heather Keller, University of Waterloo
  Purpose
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
Acute Care Medical

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective

Further study details as provided by Heather Keller, University of Waterloo:

Primary Outcome Measures:
  • 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.


Enrollment: 5995
Study Start Date: September 1, 2015
Study Completion Date: March 31, 2017
Primary Completion Date: March 31, 2017 (Final data collection date for primary outcome measure)
  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years and older   (Adult, Senior)
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
  Contacts and Locations
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
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
Principal Investigator: Heather Keller, PhD University of Waterloo
  More Information

Responsible Party: Heather Keller, Research Chair, Nutrition & Aging, University of Waterloo
ClinicalTrials.gov Identifier: NCT02800304     History of Changes
Other Study ID Numbers: 20590
First Submitted: June 7, 2016
First Posted: June 15, 2016
Last Update Posted: April 19, 2017
Last Verified: April 2017
Individual Participant Data (IPD) Sharing Statement:
Plan to Share IPD: No

Keywords provided by Heather Keller, University of Waterloo:
malnutrition
food intake
frailty