Administrative Workload in the Intensive Care Unit (AWIC)

April 25, 2019 updated by: Angelique Spoelstra-de Man, Amsterdam UMC, location VUmc

Administrative Workload in the Intensive Care Unit (AWIC Study)

A prospective observational study in the Intensive Care Unit and the Medium Care Unit in a university hospital in Amsterdam. Recent studies show that administrative tasks occupy more than 30% of the workload. One-third of these administrative tasks is unrelated to care. The administrative workload of physicians and nurses will be observed and quantified using two different methods. The amount of time physicians and nurses are logged on into the patient data management system (PDMS) will be measured and the time spent on different work tasks will be monitored with a work sampling method. Two different patient data management systems will be compared.

Study Overview

Status

Unknown

Conditions

Detailed Description

In recent years, regulatory authorities request a growing number of protocols and checklists to improve healthcare. Though the intention is to prevent medical mistakes and to improve patient care, these demands might result in an increased administrative workload for physicians and nurses. Recent studies show that administrative tasks and documentation occupy more than thirty percent of the workload of physicians, of which one-third is unrelated to care. This time spent on administration could lower the amount of time spent with the patient and the patient's family. In the Intensive Care Unit and the Medium Care Unit, most of the administrative tasks are executed within the patient data management system. The way an electronic patient data management system is set up could impact the administrative workload for physicians and nurses. A prospective observational study at the department of Intensive and Medium Care of the University medical centre will be performed with the aim to quantify the time spent on direct patient care versus administrative work. Two different patient data management systems will be compared at different points in time. The Nursing Activity Score and other patient characteristics will be registered for all the admitted patients during the two study periods.

The administrative workload of physicians and nurses will be measured before and after the implementation of a new patient data management system, using the following methods:

  • Login time in the electronic patient data management system during fourteen consecutive days in the Intensive Care Unit and the Medium Care Unit
  • Timing of activities of physicians and nurses with a work sampling method during five consecutive day shifts in the Intensive Care Unit

Study Type

Observational

Enrollment (Anticipated)

200

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Noord-Holland
      • Amsterdam, Noord-Holland, Netherlands, 1007 MB
        • Recruiting
        • VUMedicalCentre
        • Contact:
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

All patients admitted to the Intensive Care Unit during one of the two study periods

Description

Inclusion Criteria:

  • Admission to the Intensive Care Unit during one of the two study periods

Exclusion Criteria:

  • Not applicable

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Patients admitted during measurement 1
All patients admitted to the Intensive Care and Medium Care Unit during a two-week study period before the implementation of a new electronic patient data management system
Patients admitted during measurement 2
All patients admitted to the Intensive Care and Medium Care Unit during a two-week study period after the implementation of a new electronic patient data management system

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Login time in the PDMS per hour for nurses
Time Frame: 24 hours a day
The amount of time being logged on to the PDMS per hour will be calculated for different shifts
24 hours a day
Login time in the PDMS per hour for doctors
Time Frame: 24 hours a day
The amount of time being logged on to the PDMS per hour will be calculated for different shifts
24 hours a day
Amount of time spent on administrative work and documentation per shift for nurses
Time Frame: 9 hours a day
The amount of time spent on administrative tasks and documentation during dayshifts measured with a work sampling methode
9 hours a day
Amount of time spent on administrative work and documentation per shift for doctors
Time Frame: 9 hours a day
The amount of time spent on administrative tasks and documentation during dayshifts measured with a work sampling methode
9 hours a day

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Amount of time spent on direct patient care per shift for nurses
Time Frame: 9 hours a day
The amount of time spent on direct care during dayshifts measured with a work sampling methode
9 hours a day
Amount of time spent on direct patient care per shift for doctors
Time Frame: 9 hours a day
The amount of time spent on direct care during dayshifts measured with a work sampling methode
9 hours a day

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Director: Angelique ME Spoelstra - de Man, MD PhD, Amsterdam UMC, location VUmc

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

January 1, 2016

Primary Completion (Actual)

May 1, 2017

Study Completion (Anticipated)

January 1, 2020

Study Registration Dates

First Submitted

March 31, 2016

First Submitted That Met QC Criteria

March 31, 2016

First Posted (Estimate)

April 6, 2016

Study Record Updates

Last Update Posted (Actual)

April 26, 2019

Last Update Submitted That Met QC Criteria

April 25, 2019

Last Verified

April 1, 2019

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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