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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

Tracking Information
First Submitted Date June 7, 2016
First Posted Date June 15, 2016
Last Update Posted Date February 5, 2019
Study Start Date September 1, 2015
Actual Primary Completion Date March 31, 2017   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures
 (submitted: June 9, 2016)
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.
Original Primary Outcome Measures Same as current
Change History
Current Secondary Outcome Measures Not Provided
Original Secondary Outcome Measures Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title More-2-Eat; Implementation of INPAC
Official Title Not Provided
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.
Detailed Description Not Provided
Study Type Observational
Study Design Observational Model: Cohort
Time Perspective: Prospective
Target Follow-Up Duration Not Provided
Biospecimen Not Provided
Sampling Method Non-Probability Sample
Study Population medical patients over the age of 18 years
Condition Acute Care Medical
Intervention Not Provided
Study Groups/Cohorts Not Provided
Publications *

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status Completed
Actual Enrollment
 (submitted: April 18, 2017)
5995
Original Estimated Enrollment
 (submitted: June 9, 2016)
2000
Actual Study Completion Date March 31, 2017
Actual Primary Completion Date March 31, 2017   (Final data collection date for primary outcome measure)
Eligibility Criteria

Inclusion Criteria:

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

Exclusion Criteria:

  • unable to communicate in English or French
Sex/Gender
Sexes Eligible for Study: All
Ages 18 Years and older   (Adult, Older Adult)
Accepts Healthy Volunteers No
Contacts Contact information is only displayed when the study is recruiting subjects
Listed Location Countries Canada
Removed Location Countries  
 
Administrative Information
NCT Number NCT02800304
Other Study ID Numbers 20590
Has Data Monitoring Committee No
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement
Plan to Share IPD: No
Current Responsible Party Heather Keller, University of Waterloo
Original Responsible Party Same as current
Current Study Sponsor University of Waterloo
Original Study Sponsor Same as current
Collaborators University of Western Ontario, Canada
Investigators
Principal Investigator: Heather Keller, PhD University of Waterloo
PRS Account University of Waterloo
Verification Date February 2019