Post Intensive Care Syndrome
Do Improvements in Functionality on the ICU Give a Reduction of Post Intensive Care Syndrome
1 other identifier
observational
849
1 country
1
Brief Summary
Barthel Index and demographic variables of patients were collected to investigate the question whether the improvements of the functionality improves the Barthel Index over the years.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2015
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2015
CompletedFirst Submitted
Initial submission to the registry
February 16, 2016
CompletedFirst Posted
Study publicly available on registry
March 11, 2016
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2016
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2016
CompletedApril 12, 2016
April 1, 2016
6 months
February 16, 2016
April 11, 2016
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Difference in Barthel Index
barthel index is analyzed over the years 2012 - 2014
from januari 2012 until decembre 2014
Secondary Outcomes (1)
Relation between Barthel Index and length of stay in ICU
from januari 2012 until decembre 2014
Study Arms (1)
cohort 2012 - 2014
all patients admitted for \> 48 hours on the Intensive Care Unit in 2012, 2013 and 2014
Interventions
The Barthel Index for functionality is done standard in all patients after intensive care admission
Eligibility Criteria
patients treated in Intensive Care for minimal 48 hours, during the years 2012 - 2014
You may qualify if:
- years and older
- length of stay longer than 48 hours
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Medical Center Leeuwarden
Leeuwarden, 8904 BR, Netherlands
MeSH Terms
Conditions
Study Officials
- PRINCIPAL INVESTIGATOR
Matty Koopmans, MSc
MCL
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- MSc
Study Record Dates
First Submitted
February 16, 2016
First Posted
March 11, 2016
Study Start
October 1, 2015
Primary Completion
April 1, 2016
Study Completion
April 1, 2016
Last Updated
April 12, 2016
Record last verified: 2016-04
Data Sharing
- IPD Sharing
- Will not share