Post Intensive Care Syndrome

• Sponsor: Medical Centre Leeuwarden (Other)
• Overall Status: Completed
• CT.gov ID: NCT02706457
• Collaborator: (none)
• Enrollment: 849
• Location: 1
• Duration (Months): 6
• Patients Per Site Per Month: 141.2

Study Details

Study Description

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.

Condition or Disease	Intervention/Treatment	Phase
Post Intensive Care Syndrome; Barthel Index	Other: Barthel index for functionality

Detailed Description

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Study Design

• Study Type: Observational
• Actual Enrollment: 849 participants
• Observational Model: Cohort
• Time Perspective: Retrospective
• Official Title: Do Improvements in Functionality on the ICU Give a Reduction of Post Intensive Care Syndrome
• Study Start Date: Oct 1, 2015
• Actual Primary Completion Date: Apr 1, 2016
• Actual Study Completion Date: Apr 1, 2016

Arms and Interventions

Arm	Intervention/Treatment
cohort 2012 - 2014 all patients admitted for > 48 hours on the Intensive Care Unit in 2012, 2013 and 2014	Other: Barthel index for functionality; The Barthel Index for functionality is done standard in all patients after intensive care admission

Outcome Measures

Primary Outcome Measures

1. Difference in Barthel Index [from januari 2012 until decembre 2014]

   barthel index is analyzed over the years 2012 - 2014

Secondary Outcome Measures

1. Relation between Barthel Index and length of stay in ICU [from januari 2012 until decembre 2014]

Eligibility Criteria

Criteria

• Ages Eligible for Study: 18 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• 18 years and older

• length of stay longer than 48 hours

Exclusion Criteria:

• no exclusion criteria if inclusion is correct

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	Medical Center Leeuwarden	Leeuwarden		Netherlands	8904 BR

Sponsors and Collaborators

• Medical Centre Leeuwarden

Investigators

• Principal Investigator: Matty Koopmans, MSc, MCL

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.

• Responsible Party: Matty Koopmans, MSc, Medical Centre Leeuwarden
• ClinicalTrials.gov Identifier: NCT02706457
• Other Study ID Numbers: nWMO 143
• First Posted: Mar 11, 2016
• Last Update Posted: Apr 12, 2016
• Last Verified: Apr 1, 2016

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No
• Keywords provided by Matty Koopmans, MSc, Medical Centre Leeuwarden: intensive care; functionality
• Additional relevant MeSH terms: Syndrome

Study Results

No Results Posted as of Apr 12, 2016