NCT02706457

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
849

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Oct 2015

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

February 16, 2016

Completed
24 days until next milestone

First Posted

Study publicly available on registry

March 11, 2016

Completed
21 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2016

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2016

Completed
Last Updated

April 12, 2016

Status Verified

April 1, 2016

Enrollment Period

6 months

First QC Date

February 16, 2016

Last Update Submit

April 11, 2016

Conditions

Keywords

intensive carefunctionality

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

Other: Barthel index for functionality

Interventions

The Barthel Index for functionality is done standard in all patients after intensive care admission

cohort 2012 - 2014

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodProbability Sample
Study Population

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

Location

MeSH Terms

Conditions

postintensive care syndrome

Study Officials

  • Matty Koopmans, MSc

    MCL

    PRINCIPAL INVESTIGATOR

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

Locations